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INR
Array
Array
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"YEARLY"
PwC -
associate
- Digital Solutions Analytics
PwC -
associate
- Digital Solutions Analytics
PwC
2-4 Yrs
15 hrs ago
Bangalore, Mumbai
Bangalore
,
Karnataka
IN
0
Bangalore
Mumbai
Maharashtra
IN
0
Mumbai
PwC -
associate
- Digital Solutions Analytics
12-12-2019
2020-03-11
PricewaterhouseCoopers Service Delivery Center Bangalore Private Limited is a wholly owned indirect subsidiary of the US firm of PricewaterhouseCoopers - Decision Innovation Analytics Consulting DIAC an operating unit of PricewaterhouseCoopers Service - Delivery Center Bangalore Private Limited has capabilities rooted in deep strategy technology operations and industry experience The firms approach to client service is based on objectivity collaboration and an unwavering commitment to its clients best interests DIAC serves Global 2000 clients in such industries as consumer-packaged goods financial services logistics manufacturing retail and distribution telecommunications healthcare and public sector organizations - DIAC provides fast insightful analysis of complex marketing and operational issues where intelligent use of data holds the key to better decisions and actions Specific services include analytics to uncover and realize new revenue and cost savings information management to track and measure key strategic business metrics not available otherwise and information strategy to identify ways of using information to increase competitive advantage and to improve underlying information architecture for sustained cost effective delivery of higher quality information throughout the enterprise Position Experienced Associate We are looking for Experienced Associates with 2 - 4 years of experience to work in our Analytics Consulting practice in Bangalore - Experienced Associates will work as an integral part of business analytics teams in India alongside clients and consultants in the U S performing high-end analysis and providing business recommendations to project teams Education B Tech B E Masters Degree from reputed institute s Required Skills Successful candidates will have demonstrated the following skills and characteristics - Experience in analyzing complex problems and translating them to data science algorithms with due attention to computational efficiency and testing at scale - Prior experience of having worked in consulting product analytics environment - Experience with big data technologies Hadoop Hive PySpark and knowledge of distributed systems for computing and data storage - Should have experience working on Python R Pyspark Spark and good to have experience in building Statistical Machine learning and AI models - Team player and demonstrated ability to work effectively across various internal organizations and international teams - Ability to mentor and train junior team members Roles and Responsibilities - Build analytics products accelerators using a variety of big data technologies and analytics tools as required by stakeholders and create robust documentation of solutions underlying design decisions and operating procedures - Work on several large scale datasets e g internal client data external public data and new sources of data and drive analytics path to align with overall project objective develop and execute analytical module development on PwCs big data platform - Engage well with both internal and external stakeholders to understand requirements and translate them to analytical solutions - Required to meet tight deadlines and manage multiple competing priorities ability to work independently and navigate through ambiguous requirements - Manage the continuous improvement of data science and machine learning by following industry best practices What we offer - Opportunity to work with an impressive array of leading companies that are strategically dependent on information and technology Experienced Associates can expect to get broad exposure to a variety of industries and assignments - An excellent opportunity to switch careers and or focus on management consulting - An opportunity to work with fast paced and innovative environment along with a group of world class and entrepreneurial professionals
Full Time
Key Skills :
data analytics, analytics, big4, data science, big data...
Job Description:
PricewaterhouseCoopers Service Delivery Center Bangalore Private Limited is a wholly owned indirect subsidiary of the US firm of PricewaterhouseCoop...
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INR
Array
Array
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"YEARLY"
Manager/Senior
associate
- Strategy - IIM/ISB/Ivy League
Manager/Senior
associate
- Strategy - IIM/ISB/Ivy League
Trio Partners
2-8 Yrs
15 hrs ago
Bangalore
Bangalore
Karnataka
IN
0
Bangalore
Manager/Senior
associate
- Strategy - IIM/ISB/Ivy League
12-12-2019
2020-03-11
Manager Senior Associate - Strategy Roles and Responsibilities - Help develop Companys short and long term strategies and business roadmap - Evaluate new strategic initiatives and opportunities by bringing in customer and market perspective as well as understanding of companys capabilities - Conceptualize new offerings or systems and create business model and processes for them - Drive implementation of the initiatives through collaborating with cross-functional teams and contributing in external conversations - Create appropriate collaterals and documents to drive the strategic initiatives and business partnerships - Be a thought partner to other teams and support them in operational activities as required Requirement - MBA from a top tier B-School or an advanced degree in engineering statistics or mathematics with 2-8 years of management consulting experience - Exposure to a startup or some startup-related experience or experience in project management roles will be preferred but not required - Must be proficient in Excel and Powerpoint and should have sufficient experience working with these tools - Must be able to quickly ramp up understanding about new concepts business opportunities and technologies - Must be excited about getting their hands dirty in executing solutions and not merely theorizing or strategizing - Must have exceptional communication skills - written and oral and be a confident presenter - Must operate with an incredibly high bias towards action - Must be self-motivated have high sense of ownership and be able to wade through a lot of fragmentation and ambiguity with high attention to detail - Must demonstrate a high level of empathy as well as teamwork and inter-personal skills
Full Time
Key Skills :
strategy consulting, corporate strategy...
Job Description:
Manager Senior Associate - Strategy Roles and Responsibilities - Help develop Companys short and long term strategies and business roadmap - E...
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INR
Array
Array
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"YEARLY"
Amway -
associate
Manager - Indirect Procurement
Amway -
associate
Manager - Indirect Procurement
Amway
6-8 Yrs
15 hrs ago
Delhi Ncr
Delhi Ncr
Not Mentioned
IN
0
Delhi Ncr
Amway -
associate
Manager - Indirect Procurement
12-12-2019
2020-03-11
Responsibilities Include - Sources and purchases IT hardware and services including new IT platform implementation support warehousing services contract shop operations facilities office supplies and or supplies necessary for operations of an organization - In addition to Amway India requirements sourcing buyer would be also be part of the global category team and would be responsible for executing global strategies for his categories - Applies purchasing procurement methodology to achieve organizational objectives best value for the enterprise and achievement of target return on investments ROI - Works very closely with internal clients to identify sourcing needs conduct buy market profiles define acceptable service levels - Develops sourcing strategies solicits analyzes request for proposals negotiates contracts and coordinates supplier integration plan with internal client Also Includes - Compiles and analyzes statistical data to determine feasibility of buying products and to establish price objectives - Establish a supplier relationship management process with continuous improvement goals programs Monitors market dynamics and communicates changes that affect internal client needs - Compiles information to keep informed on price trends and manufacturing processes - Confers with suppliers and analyzes suppliers operations to determine factors that affect prices and determines lowest cost consistent with quality reliability and ability to meet required schedules - Reviews proposals negotiates prices selects or recommends suppliers analyzes trends follows up orders placed verifies delivery approves payment and maintains necessary records May prepare bid packages CAREER LEVEL PROFICIENT - Requires complete understanding of a broad application of techniques theoretical principles and practices of area of specialty IT sourcing - Provides solutions to a variety of problems of simple to moderate scope and complexity using application of basic standards principles theories concepts and techniques - Leads simple to moderately complex projects - Manages simple to moderately complex programs - Work is reviewed for soundness of judgment overall adequacy and accuracy Education Degree Field Related Experience BE MBA PGD Mechanical production IT IT Operations supply chain 6-8 years Hands on experience in dealing with Facilities service providers or support service providers Required Knowledge Skills Abilities and or Related Experience Thorough grasp of the following Includes - Benchmarking Benchmarking seeks to deliver enhanced business results competitive advantage through use of an on-going process of comparing and contrasting our quantitative results e g cost quality etc and processes internally and externally to determine - best in class- then identifying and implementing appropriate plans to deliver - best in class- results that meet the business needs - Business Partner Relationship Management Procurement manages relationships with our key internal Business Partners to know and understand their business needs Procurement is able to build relationships by utilizing tools such as the Joint Business Plan process initiative list management and effective persuasive selling skills - Commercial Agreements Procurement drafts and executes in partnership with Legal pertinent written agreements for ongoing requirements purchase orders leases Contracts etc and Procurement collaborates on establishment of pertinent agreements for development requirements CDAs JDAs Letters of Intent etc - Industry Analysis Industry Analysis provides the Company with competitive advantage by obtaining and analyzing information on industry supply demand dynamics production technology and cost structure feedstocks capital which is used to build effective sourcing strategies cost forecasts and negotiation positions - Competitive Analysis Competitive Analysis contributes to competitive advantage by gathering and using information about competitors- materials technologies supply base sourcing strategies suppliers material costs and processes to enable the benchmarking forecasting of competitors- material services prices and material services changes - Competitive Bidding Procurement uses competitive bidding including pre-inquiry meetings to insure our price competiveness in the market place thus deliver business results and a competitive advantage - Economic Analysis Procurement forecasts costs availability and trends of material equipment services purchased by Amway and anticipates significant short and long-term changes which may impact our sourcing and or business strategy - Linking Leveraging Delivers a competitive advantage by linking Amway business needs to supplier and industry capabilities and innovation via in-depth knowledge of industries and suppliers Links Amways supplier performance expectations with supplier capabilities and drives performance improvement as needed - Negotiation Procurement plans and carries out negotiations including development of negotiation objectives goals strategies tactics to achieve required business results with consideration for desired impact on new and existing supplier relationships - Policy Stewardship Understanding and appropriate application of principles and policies in key areas that influence our practices and behaviors in sourcing activities - Sourcing Strategy Sourcing Strategy delivers required business results by appropriately applying the concepts needed to determine develop sourcing strategies and to modify those existing strategies as required by changing business and market conditions - Supplier Analysis Supplier Analysis develops a superior understanding of supplier capability and uses that understanding to deliver that suppliers goods services technologies etc to provide optimum total value results to the business - Supplier Relationship Management SRM is used for managing key supplier relationships to deliver improved business results It is intended to drive supplier-generated value that enhances Amways competitive position with both our customers and consumers General Skills - Recognized business acumen to understand needs and engage cross functional team accordingly - Ability to multi-task and proven track record in meeting deadlines in a fast-paced environment while following the fundamental processes and prioritization - Strong leadership deep practical engineering knowledge and a proven track record for timely project delivery project management cost control and customer satisfaction - Must be able to work effectively in a team environment and will interface closely with cross and outside functions - Strong analytical skills to develop simple to moderately complex business plans - Proven technical and influence skills aligning stakeholders - Strong interpersonal written verbal communication skills with ability to communicate at all levels of the organization Experience Qualifications - 6-8 years of hands-on working experience in Logistics courier service provider - BE mechanical production IT and MBA specializing in IT Operations or supply chain
Full Time
Key Skills :
procurement, purchase, sourcing, vendor management, buying...
Job Description:
Responsibilities Include - Sources and purchases IT hardware and services including new IT platform implementation support warehousing services c...
Apply Now
INR
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Array
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"YEARLY"
Senior
associate
- Finance - CFO Office Services - Financial Services
Senior
associate
- Finance - CFO Office Services - Financial Services
Leading Financial Services Provider
5-8 Yrs
15 hrs ago
Bangalore
Bangalore
Karnataka
IN
0
Bangalore
Senior
associate
- Finance - CFO Office Services - Financial Services
12-12-2019
2020-03-11
Responsibilities Assumed Project Management - Managerial role with exposure and experience in advanced Fund Administration and Book-keeping - Determining the scope of engagements delivering project plans to clients managing timelines and driving deliverables through plans - Handling accounting of funds and multiple investment companies SPVs - Managing and reviewing projects relating to the calculation of net assets values reconciliation of capital calls and distributions partner capital statements cash and bank account reconciliation preparation of monthly quarterly financial reporting packages journal entries calculation of management fees carried interest and waterfall - Being efficient in managing the execution of all key aspects of client deliverables - Communicating directly with senior professionals such as CFOs controllers and accounting managers - Ensuring all scheduled work is completed by agreed deadlines checklists are signed and files contain all required details Managing Client Relationships - Acquiring knowledge of clients operations and general strategy - Building and managing relationships with existing clients - Understanding the overall goals of the transaction and client relationships Team Management and Leadership - Managing Mentoring a team of Analysts Associates and reporting to the Senior Vice President - Driving Projects and Process Improvements - Monitoring procedures and controls within the team and reviewing and approving the teams work daily within the stated departmental guideline Prerequisites - Excellent Communication Skills - Strong grasp of various aspects of finance and an analytical ability - Commitment and ownership - Strong eye for detail and ability to multi-task - Ability to meet client-driven deadlines demanding hours requiring time management skills - High levels of honesty integrity ability to lead a team and self-drive are essential Candidate Experience - 5 to 8 years of relevant work experience with a bachelors degree or An MBA in Finance CA with a minimum of 5 years of work experience is preferred Sr Associate CFO Office Services Location Bangalore
Full Time
Key Skills :
finance and accounts, reconciliation, ca, fund administration, fund accounting...
Job Description:
Responsibilities Assumed Project Management - Managerial role with exposure and experience in advanced Fund Administration and Book-keeping - D...
Apply Now
INR
Array
Array
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"YEARLY"
Mobikwik
associate
Director Marketing
Mobikwik
associate
Director Marketing
MobiKwik
10-12 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
Mobikwik
associate
Director Marketing
12-12-2019
2020-03-11
Responsibility - To spearhead the Marketing Communication Creative and Design team - Develop and execute hugely creative and impactful integrated advertiser messaging and marketing communications for ATL BTL digital and in-app platforms - Define and develop social media strategy and expand social media presence by capitalizing on new trends use various social media channels effectively for acquisition and salience for payments as well as fintech products of MobiKwik Devise a complete social media strategy to drive actionable results from social media campaigns - Supervise and manage the content writers to devise overall content strategy and drive more traffic and business - Ensuring SEO strategies are in line with the businesss overall goals and objectives - Work cohesively with merchant marketing and product leaders internally to ensure effective positioning of the brand and drive customer acquisition - Constantly scan the industry space consumers with a view to understand trends and implication on the brand - Identify and manage tactical strategic marketing partnerships with popular mass brands across FMCG Auto e-com and similar sectors to drive key business objectives around brand salience user acquisition and user retention - Manage relationships with external vendors and agency partners SEO Social Media Planning Buying BTL activations OOH Marketing Collaterals et al Requirement - Total 10 years of experience and at least 5 years of experience of ATL BTL Digital media planning buying Should have hands-on experience in data-driven marketing use of analytics for actionable insights mobile first or in some cases mobile-only approach search marketing digital social media communication methods - Proven leadership experience working with senior stakeholders and being able to influence them without authority - Extensive knowledge of brand development and customer acquisition Life Cycle Management via online media - Ability to think strategically and prioritize in a resource constrained environment - Proven experience in managing building and developing a high performance team - Should have experience working with a Fintech Internet company About us MobiKwik is Indias largest independent mobile payments network connecting 107 million users with more than 3 million direct merchants It enables users to discover retailers brick-and-mortar stores e-com websites m-com apps billers telcos and then start paying them with 1-tap MobiKwik is powering payments for IRCTC Uber Meru Cabs Shuttl Big Bazaar OYO Rooms Zomato Barista PVR Archies WHSmith India BookMyShow Grofers Big Basket Dominos Pizza Hut eBay ShopClues Myntra Jabong Pepperfry GoDaddy MakeMyTrip Cleartrip and Yatra The company has raised funding from Sequoia Capital American Express Tree Line Asia and Cisco Investments With MobiKwik users load money into the wallet once using cash loyalty points debit card credit card and netbanking to make secure 1-tap payments for online or offline purchases Most MobiKwik users make 10-12 purchases every month using their wallet balance across diverse use cases such as recharge bills food grocery travel cabs shopping entertainment etc Users can also make bank to bank transfers via UPI to friends and family using MobiKwik Users today enjoy MobiKwik wallet services on Android Windows and iOS mobile applications and on MobiKwik com MobiKwik aspires to be the largest source of digital transactions in India
Full Time
Key Skills :
marketing, marketing communications, digital marketing, social media, sem / seo...
Job Description:
Responsibility - To spearhead the Marketing Communication Creative and Design team - Develop and execute hugely creative and impactful integrated a...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Quantitative
research
er - Trading Firm
Quantitative
research
er - Trading Firm
Stalwart People Co.
2-5 Yrs
15 hrs ago
Delhi
Delhi
Delhi
IN
0
Delhi
Quantitative
research
er - Trading Firm
12-12-2019
2020-03-11
Quantitative Researcher - Trading Firm Job Profile - Develop and deploy completely automated systematic strategies alpha seeking and market making strategies - Using advanced mathematical techniques to model and predict market movements - Analyse large financial data sets to identify trading opportunities Skill set Required - Understanding of Algorithmic infrastructures - Working knowledge of Linux Unix and experience in C or C - Proficiency in using Python R matlab for statistical data analysis
Full Time
Key Skills :
algorithmic trading, quant, quantitative trading, financial
research
, financial analysis...
Job Description:
Quantitative Researcher - Trading Firm Job Profile - Develop and deploy completely automated systematic strategies alpha seeking and market maki...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Cartesian Consulting -
associate
/Lead - Analytics
Cartesian Consulting -
associate
/Lead - Analytics
Cartesian Consulting
1-5 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
Cartesian Consulting -
associate
/Lead - Analytics
12-12-2019
2020-03-11
Role Purpose - To be an associate who works outside his comfort zone with a wide variety of work on multiple and distinctive client in an intellectually stimulating environment Key Responsibilities - Work on developing solutions to maximize usage of analytics and decision sciences in a Marketing context Lifetime value Repeat Retention Cross Sell Mix Modelling etc - Get and understand client brief across different industries Retail Telecom Finance Travel etc - Do exploratory analysis data mining report generation - Analytical approach design Hypothesis generation and validation - Development of analytical models - Interact with client to understand the if your work is comprehendible and actionable - Hand-hold through that action - Analyze campaigns and build ROI models - Coordinate client projects and manage client expectations Desired Behaviour - Equally comfortable and adaptable between working in teams and as an individual contributor - Versatile- Able to work on a diverse range of clients and assignments with seamless transition from one to the other - Meticulous and patient- After the task at hand is completed should be able to understand clients interpretation of the same and if it is actionable Should be able to guide through each step of the actions suggested - Agility and Quick Learner - Learns quickly when facing new problems A relentless and versatile learner - Strong Project and account management skills Specialised Knowledge Required - Strong technical skills - proficiency in R Python SQL - Sound grasp of Analytics Techniques - Experience of using advance analytics techniques like Regression Time Series Modelling Segmentation Clustering etc - Client handling and account management - Marketing analytics or operations experience Other Skill Sets - Strong written communications - Is able to write clearly and succinctly in a variety of communication settings and styles Can get messages across that have the desired effect - Ability to guide the client during the action implementation - Good interpretation and presentation skills Education and Experience - Your education will be BTech BE - 1-5 years experience in Analytics including hands-on experience in model development use of advanced analytics techniques and managing client interaction
Full Time
Key Skills :
analytics, data analytics, sql, python, data mining...
Job Description:
Role Purpose - To be an associate who works outside his comfort zone with a wide variety of work on multiple and distinctive client in an intellect...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Director - Product Management - Online/Internet
associate
Director - Product Management - Online/Internet
CareerNet Technologies
7-11 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
associate
Director - Product Management - Online/Internet
12-12-2019
2020-03-11
Role Associate Director Experience 1 To manage the overall vendor ecosystem by - Performance base-lining competitive benchmarking 2 Identify the opportunity for improvement 3 Working with the vendor development team to drive critical projects 4 Resolving existing escalations and complaints 5 Manage the overall serviceability for each vendor to enhance overall performance 6 Responsible for overseeing last mile operations as central SPOC 7 Analyze different vendor performance 8 Work towards resolution of complaints escalations from customers 9 Manage last-mile serviceability of its different partners 10 Improve overall delivery performance to enhance customer experience 11 Should have strong operations and business development background 12 Must have 6 sigma certification 13 Understand Lean tools 14 To work with a vendor in developing the systems processes and convert them into strategic partners who can work at scale with reliable performance 15 Work with a strategic partner to develop overall operations 16 Make it more reliable scalable and cost-effective 17 Improve overall delivery performance to enhance customer experience 18 Responsible for overseeing last mile operations as central SPOC 19 Analyze different vendor performance 20 Should have strong operations process and business development background
Full Time
Key Skills :
online product management, it product management, lean, six sigma...
Job Description:
Role Associate Director Experience 1 To manage the overall vendor ecosystem by - Performance base-lining competitive benchmarking 2 Identify ...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Sutherland - Senior Professional/
associate
Manager - Investment Banking
Sutherland - Senior Professional/
associate
Manager - Investment Banking
Sutherland Global
6-10 Yrs
15 hrs ago
Navi Mumbai
Navi Mumbai
Maharashtra
IN
0
Navi Mumbai
Sutherland - Senior Professional/
associate
Manager - Investment Banking
12-12-2019
2020-03-11
Description Sutherland is seeking an attentive and analytical person to join us as a Sr Professional Associate Manager - Investment Banking to be responsible for providing highly customized investment research support to some of the top Investment Banking and Private Equity clients in the Sutherland Research division Responsibilities - Support the team in delivering client requests which will ultimately help end-clients in M A Advisory Research Buy Side Sell Side Research Idea Generation Pitch books Due-diligence assignments etc - Ability to interpret analyze and summarize complex data and turn it into insightful presentations charts from a Buy-Side Research perspective - Have excellent written and oral communication skills - Should be able to independently engage with Investment Banking and Private Equity clients of Sutherland with minimal supervision - Ability to lead a team and groom junior team member - Work professionally and coherently with a diverse group of executives managers and subject matter experts - Maintain knowledge and stay abreast of developments in the fields related to his her area of responsibilities - Typical deliverables include but not limited to a Pitch Books b Operational Financial Benchmarking c Precedent Transaction Analysis d Industry Sector Company Studies e Financial Modeling Valuation Absolute and Relative Valuation f Investment Memos Confidential Information Memorandums Qualifications To succeed in this position you must - Be an MBA Finance and or a Chartered Accountant - CFA Charter holder would be an added advantage but not mandatory - Have at least seven years of prior experience in Investment Banking M A Advisory Research Private Equity - Efficient in Microsoft Office products especially MS Excel and MS Power point - Be able to work in a fast-paced environment - Have strong analytical skills be able to interpret data identify trends and make suggestions for improvements - Be pro-active in developing trust and professional rapport with employees and team members work as a team-player - Have strong verbal and written communication skills be able to communicate in a clear constructive and professional manner
Full Time
Key Skills :
banking, investment banking, investment
research
, m&a, due diligence...
Job Description:
Description Sutherland is seeking an attentive and analytical person to join us as a Sr Professional Associate Manager - Investment Banking to b...
Apply Now
INR
Array
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"YEARLY"
Mobikwik - Investment Analyst - IIM/ISB/FMS/MDI
Mobikwik - Investment Analyst - IIM/ISB/FMS/MDI
MobiKwik
3-5 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
Mobikwik - Investment Analyst - IIM/ISB/FMS/MDI
12-12-2019
2020-03-11
Support the management team in the preparation and execution of transactions - Contribute to the production of presentation materials prepare transaction documents carry out due diligence and conduct market and industry research - Conduct financial assessments discounted cash flows and multiples-based analyses - Preparation of financial models investment pitches and exit strategies - Understand the transaction cycle and process steps - Procurement and evaluation of potential investment opportunities - Conduct primary and secondary research on various industries and assess the competitive landscape for potential opportunities - Contribute to the management of the post-investment of the holding company Required Skill Set Must have - Ability to create storylines and convert them into PowerPoint documents - Financial modelling - Familiarity and or keen interest in consumer technology businesses - Communication details with the ability to interact effectively with high-level professionals clients and key stakeholders in other industries - Self-motivated highly motivated and able to work independently Nice to have skills but not essential - Prior experience in the tech industry product management Previous experience and education - Previous work experience in an investment bank venture capital firm corp dev arm of tech business - Top tier MBA college - Pre-MBA candidates are welcome to apply About us MobiKwik is Indias largest independent mobile payments network connecting 107 million users with more than 3 million direct merchants It enables users to discover retailers brick-and-mortar stores e-com websites m-com apps billers telcos and then start paying them with 1-tap MobiKwik is powering payments for IRCTC Uber Meru Cabs Shuttl Big Bazaar OYO Rooms Zomato Barista PVR Archies WHSmith India BookMyShow Grofers Big Basket Dominos Pizza Hut eBay ShopClues Myntra Jabong Pepperfry GoDaddy MakeMyTrip Cleartrip and Yatra The company has raised funding from Sequoia Capital American Express Tree Line Asia and Cisco Investments With MobiKwik users load money into the wallet once using cash loyalty points debit card credit card and netbanking to make secure 1-tap payments for online or offline purchases Most MobiKwik users make 10-12 purchases every month using their wallet balance across diverse use cases such as recharge bills food grocery travel cabs shopping entertainment etc Users can also make bank to bank transfers via UPI to friends and family using MobiKwik Users today enjoy MobiKwik wallet services on Android Windows and iOS mobile applications and on MobiKwik com MobiKwik aspires to be the largest source of digital transactions in India
Full Time
Key Skills :
investment banking, financial modeling, investment
research
, venture capital, financial analysis...
Job Description:
Support the management team in the preparation and execution of transactions - Contribute to the production of presentation materials prepare tran...
Apply Now
INR
Array
Array
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"YEARLY"
Page Group -
associate
Consultant/Team Executive - Recruitment
Page Group -
associate
Consultant/Team Executive - Recruitment
Michael Page
0-2 Yrs
15 hrs ago
Mumbai, Navi Mumbai
Mumbai
,
Maharashtra
IN
0
Mumbai
Navi Mumbai
Maharashtra
IN
0
Navi Mumbai
Page Group -
associate
Consultant/Team Executive - Recruitment
12-12-2019
2020-03-11
About Michael Page Established in 1976 in London Michael Page is a global market leader in specialist recruitment With over 40 years of experience in recruiting on behalf of the worlds top employers the group has grown organically to spread across 166 offices in 34 countries with presence in all major economies in Asia As an effort to expand its India operations and nurture young talent in the region Michael Page is currently recruiting for its coveted Team Executive Programme for the Mumbai office - Our programme enables young professionals to be trained and developed to the highest standards over a period through training comprising of on-the-job primarily and theoretical courses The reward structure is constructed within a result-driven work hard play hard culture You will be responsible for - Preparation of industry sector analysis and mapping - Sourcing for candidates - Responsible for managing the candidates applications and internal coding alignment - Maintaining candidate pool and all other aspects of candidate management - Recruitment process - Assisting a team of consultants for end-to-end functions of the recruitment cycle Ad hoc projects And over a period of time interviewing candidates on a general basis and for specific assignments The Successful Applicant You must be an enthusiastic dynamic and detail-oriented individual with a strong track record of success flair for sales and a proactive team player with the ability to demonstrate excellent communication skills and self-motivation in a client facing environment With up to 0 - 2 years of experience you must be from a top tier institution and have impeccable presentation skills If you have a desire to progress in a business to business commercial environment wed like to hear from you Whats on Offer - An environment of continual learning to increase the impact of our industry leading courses workshops and on the job mentoring - We offer unparalleled career advancement opportunities including the option of overseas relocations
Full Time
Key Skills :
recruitment, talent acquisition...
Job Description:
About Michael Page Established in 1976 in London Michael Page is a global market leader in specialist recruitment With over 40 years of experience...
Apply Now
INR
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Array
Array-Array
"YEARLY"
Moglix.com -
associate
Director/Director - Category Management - IIT/NIT/IIM/ISB
Moglix.com -
associate
Director/Director - Category Management - IIT/NIT/IIM/ISB
Moglix
4-7 Yrs
15 hrs ago
Noida
Noida
Uttar Pradesh
IN
0
Noida
Moglix.com -
associate
Director/Director - Category Management - IIT/NIT/IIM/ISB
12-12-2019
2020-03-11
Associate Director Director - Category Management Role Objective - To manage and successfully drive a SBU consisting of multiple product categories over an E-commerce driven channel while achieving targets against the KPIs as per the system This role demands the candidate to be a go-getter who has a knack for problem-solving and growth hacking - The business requires acumen to disrupt the traditional procurement processes of the MSME market and bring in a more organized way of transaction The profile allows the candidate to project entrepreneurship and leadership skills which contributing towards the success of the organization Role Responsibilities - Responsible for maximizing sales and profit of the categories and achieving sales budgets while remaining competitive in the marketplace Management of topline and bottomline P L merchandise mix and price sanity - Negotiate all vendor buying agreements between the company and respective suppliers Managing end-to-end supplier relationships Work closely with suppliers majorly brands and engage them in joint business plans with a promise of growth and scale - Work with merchandising teams on promotional planning and merchandising on the sales platforms - Work with marketing teams for selecting products through online paid channels social media etc while ensuring pricing accuracy - Plan category structure as per the market while ensuring no SEO impact to improve the customer shopping experience - Monitoring product lifecycle of every product in the category and take early calls for opportunity maximization - Accurately forecasting trends planning stock and monitoring performance - Maintaining strong focus on KPIs such as Traffic CTR Conversion Bounce Rate etc - Planning and developing the product range and finalizing the pricing strategy for products - Ensuring 100 customer satisfaction through Seller brand level monitoring of the NPS score vis-avis Inventory Management Delivery SLA Product Quality Returns Cancellations etc Education - B Tech IIT NIT BITS Pilani MBA IIM ISB - Full time flagship program
Full Time
Key Skills :
category management, ecommerce, merchandising, marketing, category head...
Job Description:
Associate Director Director - Category Management Role Objective - To manage and successfully drive a SBU consisting of multiple product catego...
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INR
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"YEARLY"
OYO Rooms -
associate
/Assistant Manager - Bank Reconciliation
OYO Rooms -
associate
/Assistant Manager - Bank Reconciliation
OYO Rooms
2-7 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
OYO Rooms -
associate
/Assistant Manager - Bank Reconciliation
12-12-2019
2020-03-11
Associate Assistant Manager - Bank Reconciliation Key Deliverables 1 Perform Bank Reconciliation on a Daily Basis 2 Liaison with all the departments for closure of open items 3 Liaison with Banks on need basis 4 Preparation of MIS Dashboard month end reports 5 Supporting the month end process
Full Time
Key Skills :
reconciliation, finance and accounts, accounting...
Job Description:
Associate Assistant Manager - Bank Reconciliation Key Deliverables 1 Perform Bank Reconciliation on a Daily Basis 2 Liaison with all the dep...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
ZoomRx -
associate
Consultant - Business Analysis
ZoomRx -
associate
Consultant - Business Analysis
ZoomRx
2-5 Yrs
15 hrs ago
Chennai
Chennai
Tamil Nadu
IN
0
Chennai
ZoomRx -
associate
Consultant - Business Analysis
12-12-2019
2020-03-11
At ZoomRx we help some of the worlds biggest biopharmaceutical companies answer questions no one else can We use innovative data analytics to provide an edge to our clients within their highly competitive marketplaces Each of us takes great pride in the quality of our work which is considered among the best in the industry We have offices in Boston New York City San Francisco and Chennai and we are growing rapidly The Business Analysis team at ZoomRx is responsible for turning raw data into powerful insights and delivering those insights to our clients We seek a motivated experienced professional to join our Business Analysis Team in our Chennai office as an Associate Consultant If you love finding creative solutions to challenging and complex problems building direct and meaningful relationships with colleagues and working in a collaborative team environment we want to hear from you What - does an Associate Consultant do - Data Analysis and Insight Generation - Working with multiple pharma clients to understand the strategic context and key objectives of the project - Designing planning and implementing multiple projects - Planning project execution and internal resource requirements - Driving project execution by managing a team of associates and data scientists - Delivering impactful concise presentations to clients that incorporate cutting edge data presentation visualizations and delivery methods - To execute these responsibilities an Associate Consultant is expected to have a solid foundation of pharma experience S He is also expected to be extremely motivated independent and agile A ZoomRx Associate Consultant must possess high-quality standards sound business judgment and compelling presentation skills Who are we looking for - Masters degree in either life-sciences related OR quantitative discipline engineering economics business and strong academic credentials - Undergraduates with 3 to 5 years of experience in market research business analytics or Post Graduates with 1 5 to 3 years of relevant work experience - Exposure to and deep understanding of multiple therapeutic areas is preferred - Proficiency in leading teams - Proficiency in MS PowerPoint MS Excel and MS Word is imperative Why is ZoomRx the place for you As a ZoomRx Associate Consultant you will have a unique bundle of opportunities - A ringside seat to a rapidly-growing company - Lead client-facing teams at Fortune 500 pharma companies - Manage a team of associates and data scientists to deliver on high-visibility market research projects
Full Time
Key Skills :
data analytics, business analysis, consulting - healthcare...
Job Description:
At ZoomRx we help some of the worlds biggest biopharmaceutical companies answer questions no one else can We use innovative data analytics to provid...
Apply Now
INR
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Array
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Lendingkart - Senior Manager/
associate
Director - Corporate Communications
Lendingkart - Senior Manager/
associate
Director - Corporate Communications
Lendingkart Technologies Pvt Ltd
6-10 Yrs
15 hrs ago
Bangalore
Bangalore
Karnataka
IN
0
Bangalore
Lendingkart - Senior Manager/
associate
Director - Corporate Communications
12-12-2019
2020-03-11
Position - Senior Manager AD - Corporate Communications Responsibilities - Contributes in strategizing and driving the implementation of communication campaigns of all nature - Develops content including authored articles spokespeople quotes opinion pieces press releases pitch notes etc - Scouts for relevant media opportunities and pitching to the right segment of journalists influencers Will be responsible for seeing it through till closure - Competition mapping preparing coverage reports briefing books etc - Tracks the industry competition and media Provide insights into key trends that are relevant to Lendingkart and creates story ideas that generate buzz and coverage - Proactively develops relationships with key journalists editors analysts bloggers and other influencers in the market and leverages these relationships to achieve results Requirement - Degree or equivalent ideally in the field of PR communications or journalism - Candidate should have minimum 5 years of relevant experience - Should have excellent media relations - Able to communicate clearly concisely and confidently in written as well as spoken English - Proven track record in delivering impactful results in the press and other media - Must be comfortable working in a dynamic work environment where speed of implementation and reaction times are crucial
Full Time
Key Skills :
corporate communication, marketing, bfsi marketing, marketing head, media relations...
Job Description:
Position - Senior Manager AD - Corporate Communications Responsibilities - Contributes in strategizing and driving the implementation of communic...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Scienaptic - Data Scientist - Operations
research
Scienaptic - Data Scientist - Operations
research
Scienaptic Systems
4-5 Yrs
15 hrs ago
Bangalore
Bangalore
Karnataka
IN
0
Bangalore
Scienaptic - Data Scientist - Operations
research
12-12-2019
2020-03-11
Scienaptic is a new age AI powered credit underwriting company that offers end-to-end credit decisioning platform Scienaptics Ether platform is fundamentally disrupting the way consumer credit is administered Financial institutions looking to expand their addressable market are engaging with Ether which offers a suite of smart AI tools to better identify qualified prospects flag high-risk prospects and offer a much more comprehensive risk assessment This approach allows financial institutions to attract prospects that were previously off the map and lend profitably to a previously underserved market Our strength is built on our ability to get together a high calibre team of coders and data scientists Our diverse backgrounds offer different perspectives and new ways of thinking It encourages lively discussions inspires thought leadership and helps us build better solutions for our clients We want someone who thrives in this setting and is inspired to craft meaningful solutions through true collaboration If you- re comfortable with ambiguity excited by change and excel through autonomy Scienaptic will be the perfect place for you We are looking for an energetic and experienced person as Data Scientist The chosen candidate will be responsible for developing all aspects of data mining predictive analytic network optimization solution development to name a few Few expectations from the candidate are - Focus on developing clear and concise analytical approach for problem solving with client partnership - Strong understanding and experience in building various optimization algorithms is a must - Academic paper level understanding of math e g mixed integer linear programming mixed integer non-linear programming techniques - Experience in working with python libraries such as gurobipy and google OR tools is a must - Strong understanding of ML libraries and applications e g Neural Net SVMs boosting methods and implementation using R Python is a plus - Managing delivery of projects incl timely communication setting milestones and tracking - Experience in working on real life large messy dataset to solve real business problems Kaggle experience is a plus - Experience in working in Healthcare industry running designing and implementing simulations such as Monte Carlo simulations is an added bonus Desired Qualifications Experience for Data Science role are - Minimum 4 years of experience with machine learning analytics consulting product development - Minimum 4 years hands on coding experience with either of R Python and demonstrated strong proficiency - PhD MBA MS B Tech Masters in Operations Research Statistics Mathematics - Passionate about innovating solving bigger picture problems dealing with ambiguity - Strong presentation data visualization skills using either of Tableau d3 js is a plus
Full Time
Key Skills :
data science, data scientist, data management, machine learning, python...
Job Description:
Scienaptic is a new age AI powered credit underwriting company that offers end-to-end credit decisioning platform Scienaptics Ether platform is funda...
Apply Now
INR
Array
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"YEARLY"
associate
- Legal - Corporate & Commercial Team - Law Firm
associate
- Legal - Corporate & Commercial Team - Law Firm
Apprentice Education & Consulting Services LLP
3-5 Yrs
15 hrs ago
Bangalore
Bangalore
Karnataka
IN
0
Bangalore
associate
- Legal - Corporate & Commercial Team - Law Firm
12-12-2019
2020-03-11
Our client a full-service law firm headquartered in Bangalore is looking for an Associate to join their corporate and commercial team Roles and Responsibilities - Contract drafting - Contract reviewing - Contract negotiation - Legal research - Legal advisory - Legal and title due diligence - M A Mergers and Acquisitions Whos hiring A full-service law firm headquartered in Bangalore Apply to this job only if - Candidate having relevant experience Interested in working at a law firm - Advantages of applying to this position - Good work exposure good pay chance to work with an employee friendly law firm work-life balance Other prerequisites Good communication interpersonal and soft skills
Full Time
Key Skills :
corporate law, llb, contract management...
Job Description:
Our client a full-service law firm headquartered in Bangalore is looking for an Associate to join their corporate and commercial team Roles and Res...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Manager Market
research
Analysis Internet Online Logistics Firm
Manager Market
research
Analysis Internet Online Logistics Firm
Impeccable HR Consulting Pvt Ltd
4-8 Yrs
15 hrs ago
Mumbai
Mumbai
Maharashtra
IN
0
Mumbai
Manager Market
research
Analysis Internet Online Logistics Firm
12-12-2019
2020-03-11
Manager-Market Research and Analysis - The person will be responsible for acquiring and analyzing internal and external market information to provide inputs to the senior management in planning product development and facilitate effective decision making - Ensure the timely conduct of various market research and market intelligence studies for effective decision making including reports - Scan environment for business opportunities through external and internal research competitor intelligence etc and present findings to the senior management - Work closely with the Managing Director Head - Business Development CMO in developing the marketing sales and product strategy - Ensure the conduct of product specific research in terms of market potential competitor activities competitor pricing competitor services etc and forward the same to the respective product head - Lead the conduct of various customer satisfaction studies through appropriate coordination with the external market research agency - Support in the conduct of Annual Brand Equity study - Attend relevant industry seminars lectures to provide inputs to the senior management on market information trends and new business opportunities
Full Time
Key Skills :
market
research
, market intelligence,
research
...
Job Description:
Manager-Market Research and Analysis - The person will be responsible for acquiring and analyzing internal and external market information to provide...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Director Bra Marketing FMCG Internet Online IIM ISB FMS MDI
associate
Director Bra Marketing FMCG Internet Online IIM ISB FMS MDI
RGF Recruit India Pvt Ltd
15-18 Yrs
15 hrs ago
Bangalore
Bangalore
Karnataka
IN
0
Bangalore
associate
Director Bra Marketing FMCG Internet Online IIM ISB FMS MDI
12-12-2019
2020-03-11
Who you are A A Brand Strategist with passion for brand building who has hands-on understanding of brand development and GTM B A Brand Evangelist who will not only shape brands but has the drive to help scale and deliver on ambitious business metrics C A Brand Communication Lead who can independently craft integrated marketing plans for both ATL and Digital working in tandem with external agency partners and internal stakeholders D Above all you should be Consumer First Someone who can help distill and bring forth deep consumer insights to complex business problems Core Responsibilities A Would contribute to the Brand Development Positioning and Go-to-Market for various Category marketing initiatives B Would be the custodian of the brand as expressed for the respective categories who will define and drive adherence to brand philosophy campaign design Must haves A Ability to translate complex business and consumer tasks into brand propositions with deep consumer connect B Creative thinker with a passion for ideas and deep understanding of using digital and traditional channels as a means for brands to communicate with online audiences C Be comfortable with both creative and business dimensions of marketing D Comfortable to strategize and execute large scale branding and marketing communication campaigns E Think about brand beyond communication and develop a holistic brand experience from packaging to after sale service across consumer touch points F Understand the partner ecosystem to bring the right business partners to a project and help nurture those relationships G Be able to translate brand propositions into internal pitches as required to drive stakeholder approvals and buy-ins H Minimum 15 years of experience in a core brand management profiles having managed a complete brand development lifecycle from brand development to GTM Role Dimensions Competencies 1 A Creative Appreciation Able to choose the winning creative among a group of ideas based of a mix of technical knowledge and intuition 1 B Proposition Development Is able to articulate the problem statement and create an effective proposition 1 C Understanding Media Strategy Plans Sources and selects optimal media platforms and determines the best combination of media to achieve the marketing campaign objectives 1 D Research Orientation Showcases problem oriented and critical thinking Adapts a research based approach to problems and understands industry best practices 2 A Customer Orientation - Puts the customer at the beginning centre end of every decision 2 B Data Analytics Understands the business and the market and provides business intelligence that can be translated to actions 2 C Managing Stakeholders Forms monitors and maintains constructive relationships with stakeholders by managing their expectations and moves the project business towards its stated goals 2 D Planning The ability to think clearly and logically to understand the problem statement provide solutions where relevant and share it with relevant stakeholders 2 E Business Understanding Demonstrates keenness and quickness in understanding business and macro trends affecting business - candidates from premier institutes only
Full Time
Key Skills :
brand management, marketing, marketing communications, go to market, media planning...
Job Description:
Who you are A A Brand Strategist with passion for brand building who has hands-on understanding of brand development and GTM B A Brand Evangelist...
Apply Now
INR
Array
Array
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"YEARLY"
associate
- Knowledge Management - Pharma
associate
- Knowledge Management - Pharma
Conscript
3-9 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
associate
- Knowledge Management - Pharma
12-12-2019
2020-03-11
We seek Knowledge Management Associate to join our New Delhi India office in our Headquarters group The person in this role will research develop and maintain knowledge for the firm and will have an opportunity to partner and collaborate with thought leaders project teams and practice areas across The KM Associate role is designed for individuals who have a strong passion for knowledge and research and the people they impact They have responsibility for supporting thought leaders project teams and practice areas by collating organizing and disseminating external and collective knowledge of the firm to help our project teams and client service RESPONSIBILITIES - Assess firm knowledge needs and requirements short-term or long-term - Deliver targeted insights using internal knowledge and external sources - Help the firm prepare materials for Summits and Conferences - Support the creation and update of knowledge assets including client updates competitive intelligence industry research etc - Maintain manage and develop the firms knowledge infrastructure - Share best practices and tactical knowledge across offices practice areas and teams - Engage and build relationships with firm members and leaders
Full Time
Key Skills :
knowledge management,
research
, consulting - pharma...
Job Description:
We seek Knowledge Management Associate to join our New Delhi India office in our Headquarters group The person in this role will research develop a...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
SEO Executive
SEO Executive
Softlogic Systems Pvt Ltd
1-3 Yrs
14 hrs ago
Chennai
Chennai
Tamil Nadu
IN
0
Chennai
SEO Executive
12-12-2019
2020-03-11
Must be good in SEO SMO SEM techniques Focus towards Lead Generation Creating SMM strategies to create a brand name in Social Media and raise awareness Evaluating competitor s strategies and creating plans to overtake them
Full Time
Key Skills :
adsense, adwords, wordpress cms, google analytics, link building...
Job Description:
Must be good in SEO SMO SEM techniques Focus towards Lead Generation Creating SMM strategies to create a brand name in Social Media and rais...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Business
research
/Industry
research
Role - Big4
Business
research
/Industry
research
Role - Big4
Spectral Consulting
2-7 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
Business
research
/Industry
research
Role - Big4
12-12-2019
2020-03-11
Role Qualitative and Quantitative Research Location Gurgaon Gurugram Role Description Executing quantitative qualitative research for various M A projects Job Description KRAs - Perform qualitative and quantitative research on the markets and or target companies - Involved in analyzing various investment banking products including M A analysis benchmarking analysis and transaction analysis - Conducting secondary research using several databases and drawing insights from the available data Desired Candidate - MBA or CA with 2 5-6 years - Expert knowledge of Qualitative and Quantitative research and databases such as Capital IQ One Source Factiva and Merger Market
Full Time
Key Skills :
big4,
research
, ca, financial
research
...
Job Description:
Role Qualitative and Quantitative Research Location Gurgaon Gurugram Role Description Executing quantitative qualitative research for various ...
Apply Now
INR
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Array
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"YEARLY"
Client
associate
s -
associate
- Asset Allocation
Client
associate
s -
associate
- Asset Allocation
Client Associates
5-7 Yrs
15 hrs ago
Delhi Ncr, Gurgaon, Gurugram
Delhi Ncr
,
Not Mentioned
IN
0
Delhi Ncr
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
Client
associate
s -
associate
- Asset Allocation
12-12-2019
2020-03-11
Develop financial models and analysis relevant to making recommendations over the tactical and strategic investment horizons - Use financial principles to develop a systematic data-driven approach to formulating modeled returns and risks for significant asset classes and constructing optimal portfolios - Develop and refine models for security selection evaluations of investment products and portfolios examination of current markets for attractiveness of active and passive management and analysis of current and timely investment controversies - Strong knowledge of MF Non MFs - Should have deep knowledge of EQ Portfolio performance Alpha EQ HYB - Handle clients queries related to Asset Allocation
Full Time
Key Skills :
asset management, financial modeling, portfolio management...
Job Description:
Develop financial models and analysis relevant to making recommendations over the tactical and strategic investment horizons - Use financial prin...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
PwC -
associate
- IoT Analytics
PwC -
associate
- IoT Analytics
PwC
2-4 Yrs
15 hrs ago
Bangalore, Mumbai
Bangalore
,
Karnataka
IN
0
Bangalore
Mumbai
Maharashtra
IN
0
Mumbai
PwC -
associate
- IoT Analytics
12-12-2019
2020-03-11
PricewaterhouseCoopers Service Delivery Center Bangalore Private Limited is a wholly owned indirect subsidiary of the US firm of PricewaterhouseCoopers Decision Innovation Analytics Consulting - DIAC- a business unit of PwC Service Delivery Center Bangalore Private Limited has capabilities rooted in deep strategy technology operations and industry experience The firms approach to client service is based on objectivity collaboration and an unwavering commitment to its clients best interests DIAC serves Global 2000 clients in such industries as consumer packaged goods financial services logistics manufacturing retail and distribution telecommunications healthcare and public sector organizations - DIAC provides fast insightful analysis of complex marketing and operational issues where intelligent use of data holds the key to better decisions and actions Specific services include analytics to uncover and realize new revenue and cost savings information management to track and measure key strategic business metrics not available otherwise and information strategy to identify ways of using information to increase competitive advantage and to improve underlying information architecture for sustained cost effective delivery of higher quality information throughout the enterprise Level Associate 2 - We are looking for experienced leaders with strong analytics background and overall professional experience of 2 - 4 years to work in our Analytics Consulting practice in Mumbai - Associate 2 will work as an integral part of business analytics teams in India alongside clients and consultants in the U S leading teams for high-end analytics consulting engagements and providing business recommendations to project teams - Level of Education Specific Schools BTech MTech Masters in Economics Statistics Mathematics MBA PhD typically from following schools like NIT IIT IGIDR Delhi School of Economics IIM ISB or any other reputed school Required Skills Successful candidates will have demonstrated the following skills and characteristics - Prior experience of having worked in consulting analytics environment - Ability to structure projects engagements for the team - Strong verbal and written communication and presentation skills - Experience of engaging with International clients and working in onsite-offshore environment - Ability to contribute beyond the defined scope of work - Strong aptitude along with good academic and professional background - Demonstrated experience of contributing in firm and knowledge building - Hands on experience with multiple types of modern deep learning architecture - Experience of working on hardware sensors device prototyping and edge computing Role - Candidate should have inclination towards creative ideas experimenting and working in advanced innovation driven environment keeping industry demand and applicability of such experiments in consulting engagements - This role is for hands-on analytics data scientist with mindset of AI driven innovation in different platforms with new and emerging techniques - Candidate should be oriented to work in high performing team environment and lead other team members - Experience and acquaintance with some or most of the below mentioned areas is what we are looking for - Must have hands on Python experience e g Pandas OpenCV pybrain Scikit etc - Working experience in sensor programing edge device computing mobile GPUs hardware prototyping etc - Experience interfacing IoT devices to cloud computing environment - Should have implementation knowledge of advanced applications like image and motion analytics NLP techniques word2vec Topic modeling audio processing etc and deep learning What we offer 1 Opportunity to work with an impressive array of leading companies that are strategically dependent on information and technology 2 Senior Associates would typically be tagged to an industry of specialization or choice with the opportunity of cross-industry movement 3 An excellent opportunity to switch careers and or focus on analytics embedded consulting 4 An opportunity to work with fast paced
Full Time
Key Skills :
python, analytics, data analytics, internet of things, big4...
Job Description:
PricewaterhouseCoopers Service Delivery Center Bangalore Private Limited is a wholly owned indirect subsidiary of the US firm of PricewaterhouseCoo...
Apply Now
INR
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Array
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PwC - Senior
associate
- Digital Solutions Analytics
PwC - Senior
associate
- Digital Solutions Analytics
PwC
4-7 Yrs
15 hrs ago
Bangalore, Mumbai
Bangalore
,
Karnataka
IN
0
Bangalore
Mumbai
Maharashtra
IN
0
Mumbai
PwC - Senior
associate
- Digital Solutions Analytics
12-12-2019
2020-03-11
PricewaterhouseCoopers Service Delivery Center Bangalore Private Limited is a wholly owned indirect subsidiary of the US firm of PricewaterhouseCoopers - Decision Innovation Analytics Consulting DIAC an operating unit of PricewaterhouseCoopers Service Delivery Center Bangalore Private Limited has capabilities rooted in deep strategy technology operations and industry experience The firms approach to client service is based on objectivity collaboration and an unwavering commitment to its clients best interests DIAC serves Global 2000 clients in such industries as consumer-packaged goods financial services logistics manufacturing retail and distribution telecommunications healthcare and public sector organizations - DIAC provides fast insightful analysis of complex marketing and operational issues where intelligent use of data holds the key to better decisions and actions Specific services include analytics to uncover and realize new revenue and cost savings information management to track and measure key strategic business metrics not available otherwise and information strategy to identify ways of using information to increase competitive advantage and to improve underlying information architecture for sustained cost effective delivery of higher quality information throughout the enterprise Position Experienced Associate We are looking for Experienced Associates with 2 - 4 years of experience to work in our Analytics Consulting practice in Bangalore - Experienced Associates will work as an integral part of business analytics teams in India alongside clients and consultants in the U S performing high-end analysis and providing business recommendations to project teams Education B Tech B E Masters Degree from reputed institute s Required Skills Successful candidates will have demonstrated the following skills and characteristics - Experience in analyzing complex problems and translating them to data science algorithms with due attention to computational efficiency and testing at scale - Prior experience of having worked in consulting product analytics environment - Experience with big data technologies Hadoop Hive PySpark and knowledge of distributed systems for computing and data storage - Should have experience working on Python R Pyspark Spark and good to have experience in building Statistical Machine learning and AI models - Team player and demonstrated ability to work effectively across various internal organizations and international teams - Ability to mentor and train junior team members Roles and Responsibilities - Build analytics products accelerators using a variety of big data technologies and analytics tools as required by stakeholders and create robust documentation of solutions underlying design decisions and operating procedures - Work on several large scale datasets e g internal client data external public data and new sources of data and drive analytics path to align with overall project objective develop and execute analytical module development on PwCs big data platform - Engage well with both internal and external stakeholders to understand requirements and translate them to analytical solutions - Required to meet tight deadlines and manage multiple competing priorities ability to work independently and navigate through ambiguous requirements - Manage the continuous improvement of data science and machine learning by following industry best practices What we offer - Opportunity to work with an impressive array of leading companies that are strategically dependent on information and technology Experienced Associates can expect to get broad exposure to a variety of industries and assignments - An excellent opportunity to switch careers and or focus on management consulting - An opportunity to work with fast paced and innovative environment along with a group of world class and entrepreneurial professionals
Full Time
Key Skills :
data analytics, analytics, big4, data science, big data...
Job Description:
PricewaterhouseCoopers Service Delivery Center Bangalore Private Limited is a wholly owned indirect subsidiary of the US firm of PricewaterhouseCoo...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
VMock -
associate
Product Manager
VMock -
associate
Product Manager
VMock
1-5 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
VMock -
associate
Product Manager
12-12-2019
2020-03-11
VMock is an AI ML based SMART Career Preparation Platform that combines the power of cutting-edge data analytics and sophisticated technology to provide personalized feedback to students and alumni It is currently being used by students alumni and career centres across 120 leading global universities and business schools The company also boasts of investors who have been Directors at McKinsey SF office EVP Bain Capital White House Champions of Change Award recipient as great entrepreneurs and several others - We are a team of technical minds engineering experts thinkers and innovators bringing intelligent automation in the career development space People at VMock are ambitious young leaders from some of the best institutes from around the world with skills and zeal to solve the toughest problems They work with innovation at its bleeding edge and are passionate about building products to change the shape of a persons professional journey Machine learning advanced analytics natural language processing and state-of-the-art engineering and unparalleled technology are at the core of VMocks specialized products - People at VMock are collaborators at heart and support each other in learning and developing indulging in knowledge sharing while having thoughtful discussions on bringing unparalleled innovation using technology - If you have the willingness to exceed beyond definitive job roles and if you want to work at a place that will challenge you to push your boundaries every day VMock is the place for you Responsibilities - Manage the entire life cycle of a product from inception to launch - Lead a team define and shape customer experience deliver new features and products - Understand and articulate customer needs conduct on-going customer research leverage internal knowledge and expertise and prioritize customer requirements - Identify market opportunities and define product vision and strategy - Define product roadmaps based on leaderships strategy and vision - Understand customer needs and gather product requirements - Engage closely with the engineering team and other stakeholders Analysts Sales Marketing and Business teams to guide ideas and products from inception to launch - Handle complex ideas and break them down into concise and effective requirements to drive product development - Define implement and monitor Key Performance Indicators for product effectiveness Requirements - Strong academic background - UG in engineering from tier -1 institutes and MBA from a top - tier business school India or abroad - 1 years of demonstrated experience of developing products from concept to launch - Experience in Product Lifecycle Management - Deep understanding of customers- needs and aspirations - Passionate about using technology to solve real world business problems - Understanding of how customer requirements are translated into meaningful products - Coding and development experience preferred - Leadership DNA with proven ability to excite and lead a cross-functional engineering team - Excellent problem-solving organizational and analytical skills
Full Time
Key Skills :
it product management, it product development...
Job Description:
VMock is an AI ML based SMART Career Preparation Platform that combines the power of cutting-edge data analytics and sophisticated technology to prov...
Apply Now
INR
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Array
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"YEARLY"
159Solutions - Analytics
associate
Consultant
159Solutions - Analytics
associate
Consultant
159 Solutions
2-3 Yrs
15 hrs ago
Pune
Pune
Maharashtra
IN
0
Pune
159Solutions - Analytics
associate
Consultant
12-12-2019
2020-03-11
Does working closely with a small and driven group of entrepreneurs intrigue you- - Does solving complex problems in a fast paced and unstructured environment excite you- - Does the idea of wearing multiple proverbial hats and challenging yourself to achieve goals delight you- - Do you see yourself managing driven analysts to deliver high quality analytics- If you answered YES to the above questions read on 159 Solutions was founded to solve a key gap among analytics providers - lack of business context Unlike larger firms that provide limited engagement of senior members we model our teams in a way that allows our partners to be actually staffed on projects We are focused on healthcare - specifically Oncology and Specialty therapeutics and devices that allow us to build deep expertise to make a difference to our clients We are looking for Analytics Associate consultants in Pune India who thrive on the challenge of using complex data to solve critical business problems Our ACs work with consultants or managers to create custom solutions by leveraging disparate data sources to support sales and marketing decisions ACs will be responsible for substantial portion of analyses from problem formulation to solution creation Job description Associate consultants will have the opportunity to leverage a wide variety of skills - Process large-scale healthcare datasets using SAS R SQL other database management tools - Develop advanced statistical models that relate promotion and product sales - Build simulation models using Excel VBA to assess the effects of sales and marketing programs based on different permutation combinations - Perform exploratory and predictive analytics CART ridge regression SVM etc to address complex business problems - Assist with creation of PowerPoint slides and online visualization e g highcharts Qlik etc to communicate findings - Mentor junior associates and assist with multiple work streams to deliver high quality deliverables on time - Advance analytics knowledge base and assist with new capabilities development Responsibilities The position is expected to work at least 40 hours per week and distribute work as per the tasks assigned Heres an approximate breakout of time spent on different tasks - Processing data and building integrated datasets for analysis 30 - Building advanced statistical models 30 - Preparing presentation materials to communicate results 15 - Project and team management and firm contribution 15 - Advancing analytics knowledge and training 10 Consulting is a fast-paced environment and the candidate should be open to learning new skills quickly and deliver work under tight timelines The candidates needs to be flexible working with multiple clients and managing analysis to deliver high quality work The position will be responsible for delivering high quality work under consultant supervision and guidance from the Principal Manager Qualifications 159 solutions seeks candidates with strong programming database management and statistics and mathematics background We welcome candidates with at least a bachelors degree in computer science business analytics engineering or related quantitative disciplines - Two years of experience in quantitative analysis - Strong skills in manipulation of large complex data sets - Ability to quickly learn the basics of healthcare and become proficient in the use of proprietary data sets - High motivation strong work-ethic and positive attitude while working under tight timelines - Strong attention to detail and focus on quality - Team management and Excel VBA experience would be a plus - Willingness to mentor associates and dedication to continuous learning
Full Time
Key Skills :
analytics, data analytics, data management, sas, statistics...
Job Description:
Does working closely with a small and driven group of entrepreneurs intrigue you- - Does solving complex problems in a fast paced and unstructured ...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Head -
research
& Development - FMCG
Head -
research
& Development - FMCG
Fintellect Consultancy Services Private Limited
10-20 Yrs
15 hrs ago
Noida
Noida
Uttar Pradesh
IN
0
Noida
Head -
research
& Development - FMCG
12-12-2019
2020-03-11
Conceptualise new products and projects - Improvement of existing products and formulations - Identify suitable areas of research for future growth - Conduct collaborative research with various research institutes in India and abroad - Provide technical support to domestic marketing teams - Provide analysis on technical matters to operations team and Head SBU - Planning and timely implementation of Capex items
Full Time
Key Skills :
r&d, new product development, new product design...
Job Description:
Conceptualise new products and projects - Improvement of existing products and formulations - Identify suitable areas of research for future gro...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Senior
associate
/Assistant Manager/Manager - Business Tax
Senior
associate
/Assistant Manager/Manager - Business Tax
Contactx
3-10 Yrs
15 hrs ago
Bangalore
Bangalore
Karnataka
IN
0
Bangalore
Senior
associate
/Assistant Manager/Manager - Business Tax
12-12-2019
2020-03-11
Excellent opportunity in Big 4 For Bangalore Location Any candidate ready for Relocation to Bangalore will be consider for this position Roles and responsibilities US Tax- Business Tax - The Tax Senior is responsible for reviewing trust partnership and corporate tax returns preparing complex tax returns and assisting in reporting and MIS activities - Experience into 1065 1120 - Strong tax accounting skills with proficiency in US GAAP and tax compliance - Understanding of Federal taxes - Broad exposure to Federal income taxation and knowledge of tax regulations - Ability to perform FAS 109 tax provisions Qualification Graduate MBA M com CA Post Qualification atleast 3 Years of relevant Experience required Excellent communication Skills
Full Time
Key Skills :
direct tax, taxation, ca...
Job Description:
Excellent opportunity in Big 4 For Bangalore Location Any candidate ready for Relocation to Bangalore will be consider for this position Roles and ...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Flipkart -
associate
Director - Performance Development
Flipkart -
associate
Director - Performance Development
Flipkart
10-12 Yrs
15 hrs ago
Bangalore
Bangalore
Karnataka
IN
0
Bangalore
Flipkart -
associate
Director - Performance Development
12-12-2019
2020-03-11
Flipkart - Associate Director - Performance Development Responsibilities - Build and execute end to end performance strategy with a strong focus on driving a culture of meritocracy risk-taking innovation and collaboration - Lead and own the performance cycle which includes working closely with stakeholders across levels and continuously enhancing the effectiveness of the processes - Develop and implement ideas for improving the performance process and outcomes by collecting feedback and insights to identify areas of improvement and ensuring buy-in of the various stakeholders - Lead the SVP and VP ratings and promotions processes - Be the champion of organizational values and ensure alignment across performance as well as other org-wide HR processes - Create define dashboards metrics measurements of success and conduct regular reporting to key stakeholders - Benchmark best practices from the market and leverage wherever applicable - Design review oversee and ensure compliance of various processes policies systems Desired skills and experience - Candidates with 10 years of extensive HR experience with a relevant degree in human resources - Collaborative approach effective program management experience and an ability to influence senior leadership regarding critical talent decisions - Analytical problem solving - People centric approach - Subject matter expertise in the areas of talent development performance assessment and business partnering - Must have a broad understanding of the external market - Relevant experience in E-Commerce Retail FMCG Supply Chain industry preferred
Full Time
Key Skills :
hr head, hr business partner, performance management, talent development, ecommerce...
Job Description:
Flipkart - Associate Director - Performance Development Responsibilities - Build and execute end to end performance strategy with a strong focu...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Manager/Senior
associate
- Risk Advisory - Consulting Firm - CA
Manager/Senior
associate
- Risk Advisory - Consulting Firm - CA
Phenom Placements
3-9 Yrs
15 hrs ago
Overseas, International, Mauritius
Overseas
,
Not Mentioned
IN
0
Overseas
International
,
Not Mentioned
IN
0
International
Mauritius
Not Mentioned
IN
0
Mauritius
Manager/Senior
associate
- Risk Advisory - Consulting Firm - CA
12-12-2019
2020-03-11
Employer MNC Consulting Firm Job Location Mauritius Position Title Senior Associate Manager CA 3 yrs Accommodation Will not be provided by the employer Department Risk Advisory Role Responsibilities As a senior Associate Manager you will be Ensuring successful completion of assigned engagements from start to finish Depending on assigned engagement reports to one or more member s of the Senior Management team Technical Capabilities a Identifies and communicates issues raised offering recommended solutions relevant to business b Performs other related duties as assigned Leadership Supervisory Skills a Supervises Associates assigned to engagements providing guidance and overall review of deliverables b Organizes personal effort along with those of juniors to be risk-based productive and efficient at all times c Ensures adequate focus on personal professional growth relevant to taking on more challenging assignments in line with standard career progression - proactively seeks relevant Education and training opportunities Communication a Ensures adherence at all times to all applicable department and professional standards Communicates assigned tasks to engagement team in a manner that is clear and concise ensuring high quality accurate and efficient results and takes corrective actions when needed Client Relationship a Interact with clients to help ensure that the information flow from the client to the team is efficient If you are interested please share your updated CV along with the following details 1 Current Company 2 Current CTC 3 Expected CTC 4 Notice Period 5 Skype ID 6 OK for Mauritius 8 Marital Status Ankur
Full Time
Key Skills :
risk management, ca...
Job Description:
Employer MNC Consulting Firm Job Location Mauritius Position Title Senior Associate Manager CA 3 yrs Accommodation Will not be prov...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Vice President - Credit Analyst - Fixed Income - Investment Banking
associate
Vice President - Credit Analyst - Fixed Income - Investment Banking
Thema Corporate Services LLP
7-9 Yrs
15 hrs ago
Mumbai, Navi Mumbai
Mumbai
,
Maharashtra
IN
0
Mumbai
Navi Mumbai
Maharashtra
IN
0
Navi Mumbai
associate
Vice President - Credit Analyst - Fixed Income - Investment Banking
12-12-2019
2020-03-11
Designation - Associate Vice President Band 3 Credit Research Analyst Role Specs - Credit assessment of existing and new issuers from financial and non-financial sectors interactions with management credit rating agencies bankers and other market participants - Preparing credit notes encompassing quantitative and qualitative factors on regular frequency based on internal risk assessment sharing outlook on credit rating movements and recommending exposure limits and tenor to the investment committee and fund managers - Maintaining updated dashboard on existing set of issuer universe for fund management audit and risk control - Assess industry trends and client financial performance changing industry trends and provide forward looking views in the analysis - Tracking industry and macro parameters and support fund manager in developing portfolio management strategies and presenting it to investment committee fund managers and other functions
Full Time
Key Skills :
credit analysis, fixed income, credit risk, investment banking, banking...
Job Description:
Designation - Associate Vice President Band 3 Credit Research Analyst Role Specs - Credit assessment of existing and new issuers from financial ...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Sutherland - Senior Professional/
associate
Manager - Investment Banking
research
Sutherland - Senior Professional/
associate
Manager - Investment Banking
research
Sutherland Global
6-9 Yrs
15 hrs ago
Navi Mumbai
Navi Mumbai
Maharashtra
IN
0
Navi Mumbai
Sutherland - Senior Professional/
associate
Manager - Investment Banking
research
12-12-2019
2020-03-11
Description Sutherland is seeking an attentive and analytical person to join us as a Sr Professional Associate Manager - Investment Banking to be responsible for providing highly customized investment research support to some of the top Investment Banking and Private Equity clients in the Sutherland Research division Responsibilities - Support the team in delivering client requests which will ultimately help end-clients in M A Advisory Research Buy Side Sell Side Research Idea Generation Pitch books Due-diligence assignments etc - Ability to interpret analyze and summarize complex data and turn it into insightful presentations charts from a Buy-Side Research perspective - Have excellent written and oral communication skills - Should be able to independently engage with Investment Banking and Private Equity clients of Sutherland with minimal supervision - Ability to lead a team and groom junior team member - Work professionally and coherently with a diverse group of executives managers and subject matter experts - Maintain knowledge and stay abreast of developments in the fields related to his her area of responsibilities - Typical deliverables include but not limited to a Pitch Books b Operational Financial Benchmarking c Precedent Transaction Analysis d Industry Sector Company Studies e Financial Modeling Valuation Absolute and Relative Valuation f Investment Memos Confidential Information Memorandums Qualifications To succeed in this position you must - Be an MBA Finance and or a Chartered Accountant - CFA Charter holder would be an added advantage but not mandatory - Have at least seven years of prior experience in Investment Banking M A Advisory Research Private Equity - Efficient in Microsoft Office products especially MS Excel and MS Power point - Be able to work in a fast-paced environment - Have strong analytical skills be able to interpret data identify trends and make suggestions for improvements - Be pro-active in developing trust and professional rapport with employees and team members work as a team-player - Have strong verbal and written communication skills be able to communicate in a clear constructive and professional manner
Full Time
Key Skills :
investment banking, ca, cfa, valuation, due diligence...
Job Description:
Description Sutherland is seeking an attentive and analytical person to join us as a Sr Professional Associate Manager - Investment Banking to be...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Egon Zehnder - Senior
research
Analyst - Consumer
Egon Zehnder - Senior
research
Analyst - Consumer
Egon Zehnder - Knowledge Center India
5-8 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
Egon Zehnder - Senior
research
Analyst - Consumer
12-12-2019
2020-03-11
Company Egon Zehnder EZ is one of the worlds top five retained executive search-consulting firms EZs clients range from the largest multinationals to emerging growth companies government and regulatory bodies and major educational and cultural institutions We work at the highest levels of leadership to create tangible and enduring business impact Our core services include Executive Search Board Consulting and Leadership Strategy Services Opportunity This is an exciting opportunity to join the Research division of Egon Zehner Knowledge Center India Collaboration is at the heart of our culture Our structure is flat and informal and information therefore flows freely Working at Egon Zehnder will allow researchers to develop a deep understanding of that human capital element Many researchers already know how to understand companies products and industries Learning the very difficult skill of identifying and assessing senior managers and how talent pools and careers move will bring a major new perspective to understanding businesses About This Role - The role is broad based covering business development search and knowledge management - Researchers accompany a project from the beginning to the end working very closely with consultants Researchers see the whole context and are expected to contribute to discussions on search strategy and the suitability of candidates - Aligned by industry or functional practice group researchers can leverage their industry domain expertise and grow as knowledge experts and knowledge managers - We offer international training programmes and the ability to collaborate with colleagues globally Required skills and experience - Project Management Time management managing deadlines managing multiple projects utilizing right resources and problem solving - Delivering Output Documents Producing high quality content of relevant documents - Collaboration and Teamwork Partnering with others on projects and contributing as a part of the team - Communication Skills Confident and strong communicator and have a professional demeanor - Proactive A deep knowledge of or clear propensity to learn Industry at large its competitive landscape including the latest trends Location Gurgaon Sector 32 Contact no 0124-4755905
Full Time
Key Skills :
project management,
research
...
Job Description:
Company Egon Zehnder EZ is one of the worlds top five retained executive search-consulting firms EZs clients range from the largest multinationa...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Vice President - Corporate Sales - General
associate
Vice President - Corporate Sales - General
Fortune HR Consultant
7-17 Yrs
15 hrs ago
Gujarat, Vadodara, Baroda
Gujarat
,
Not Mentioned
IN
0
Gujarat
Vadodara
,
Gujarat
IN
0
Vadodara
Baroda
Not Mentioned
IN
0
Baroda
associate
Vice President - Corporate Sales - General
12-12-2019
2020-03-11
Client Name Leading General Company Location Open Baroda in Gujarat Candidate only from Tier 1 2 Associate Vice President - Corporate Solutions Group The role will manage all the General needs of Corporate Clients - Meeting corporate client and explain business proposition products and services and offer General Products like - Fire - Factory - Marine - Travel - Burglary - Liability - Directors Policy ETC - Carry out policy closure related activities both concerning the client and internal company processes - Track Clients portfolio on general - Meet sales and client acquisition targets on monthly basis - To devise new strategies to assist clients given the changing market conditions e g reviewing claim ratio
Full Time
Key Skills :
corporate sales, sales, institutional sales, b2b sales, bfsi sales...
Job Description:
Client Name Leading General Company Location Open Baroda in Gujarat Candidate only from Tier 1 2 Associate Vice President - Corporate Soluti...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
/Senior
associate
- Data Management - Python/Spark SQL/Collibra - BFSI
associate
/Senior
associate
- Data Management - Python/Spark SQL/Collibra - BFSI
Pylon Management Consulting Pvt. Ltd.
5-10 Yrs
15 hrs ago
Mumbai
Mumbai
Maharashtra
IN
0
Mumbai
associate
/Senior
associate
- Data Management - Python/Spark SQL/Collibra - BFSI
12-12-2019
2020-03-11
Client - MNC Bank Location - Mumbai Position - Associate Sr Associate Data Management Education - Any grad Post grad Full time Experience - 5-9 yrs Job Description - 1 Set up and manage framework for systemic data storage and access covering all parts of the business and its operational processes 2 Facilitate adoption of Project Singularity for the country - provide timely inputs on metadata models data structures and ensure coverage of all aspects of India business operations 3 Drive data quality and accuracy a Work closely with finance and operations to operationalize data reconciliation framework to ensure a single view of truth across functions b Establish measurable metrics for data quality - setup periodic monitoring framework c Drive frontline data capture quality through systematic process enhancements and liaise with frontline for adoption Experience - - Experience of data management preferably in BFSI - Strong knowledge of data models data structures and reconciliation - Familiarity with ETL processes - Hands on expertise of data management tools like Python Spark SQL Collibra - Knowledge of Indian BFSI space preferred - Experience of multi-tasking and managing multiple stakeholders
Full Time
Key Skills :
data management, python, data quality, consulting - bfsi, data modeling...
Job Description:
Client - MNC Bank Location - Mumbai Position - Associate Sr Associate Data Management Education - Any grad Post grad Full time Experience...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
General Manager - Product Management - Real Estate Group - IIM//FMS/MDI/XLRI
General Manager - Product Management - Real Estate Group - IIM//FMS/MDI/XLRI
B Placed Pvt Ltd
10-15 Yrs
15 hrs ago
Chennai, Hyderabad
Chennai
,
Tamil Nadu
IN
0
Chennai
Hyderabad
Telangana State
IN
0
Hyderabad
General Manager - Product Management - Real Estate Group - IIM//FMS/MDI/XLRI
12-12-2019
2020-03-11
GM - Product Management Position Summary The incumbent will drive the product strategy for a specific market region The focus will be on both new and existing offerings Purpose will be to identify new opportunities in the present or near future make optimum use of our land bank to best respond to market and customer demand and also ensure existing products are consistently meeting the original customer promise and help promote future offerings Role Responsibilities - Strategy - - Formulating the strategy for developing land bank and planning future growth of business in the region - Comprehensive study of region with respect to supply and demand development potential Opportunity analysis to identify trends and new concepts - Drawing insights from market research into project design planning and pricing - Identification of companys key differentiators and development areas based on client satisfaction surveys and market feedback - Track competitor activity in the region from a new launch concepts pricing etc perspective Product management - - Finalization of product mix planning and project strategy in coordination with other departments - Developing project business plans Conducting studies and research around project feasibility and costs - Conducting sensitivity analysis with respect to various input parameters - Risk Management across projects and the region to identify trends and take pre-emptive corrective actions - Being the coordination point for all departments agencies to ensure costs timelines are within committed parameters - Act as the product owner for handed over projects by ensuring product promise and DLF brand values are consistently maintained Qualification Experience - Bachelors in architecture from a reputed college MBA from a Premier Business school - 10 -15 years of experience working in India time abroad will be advantageous with reputed Developers RE focused Funds Leading facility management firms IPCs - Proven track record in project management - Strong financial analytical acumen - Well networked in the RE space - Exposure to market research tools - Personal Traits Competencies - Excellent coordination skills - Strong Systems Process orientation - Good Communication interpersonal skills - Maturity to deal with a variety of people - High energy level - Customer Orientation Age - 35 - 40 Years
Full Time
Key Skills :
product management, market
research
, real estate marketing, marketing, marketing head...
Job Description:
GM - Product Management Position Summary The incumbent will drive the product strategy for a specific market region The focus will be on both ne...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Egon Zehnder - Senior
research
Analyst - Technology & Communications Sector
Egon Zehnder - Senior
research
Analyst - Technology & Communications Sector
Egon Zehnder - Knowledge Center India
5-8 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
Egon Zehnder - Senior
research
Analyst - Technology & Communications Sector
12-12-2019
2020-03-11
For the position Senior Research Analyst - Technology and Communications T C Company Egon Zehnder is the worlds leadership consulting advisory firm sharing one goal to transform people organizations and the world through great leadership As One Firm our more than 400 Consultants in 69 offices and 41 countries bring our individual strengths to form one powerful collaborative team We partner closely with public and private corporations family-owned enterprises and non-profit and government agencies to provide Board advisory services CEO search and succession executive search executive assessment leadership development and organizational transformation Egon Zehnder Knowledge Center India EZ KCI The Research Team is a group of experts aligned to specific Industry or Functional Practice that works on with global teams in solving client mandates The Researchers provide insights from internal external databases expert perspectives on industry trend and through their experiences Most of the team members come with an industry specialization working in consulting or industry or both and deliver insights for solving critical client problems Roles Responsibilities - The role is broad based covering business development search assignment execution and knowledge management - This is an individual contributor role which requires extensive collaboration and engagement with colleagues in Global office This role will be visible to clients and will be expected to help develop key account strategies Required knowledge experience - 5-8 years of professional experience in Industry Consulting or Research with deep knowledge of the Technology Industry at large its competitive landscape including the very latest trends - Experience of working on international engagements in a professional services environment with an understanding of Global market - A self-starter with learning agility engaging remotely thought partnering critical thinking eye for detail conceptual thinking Location Egon Zehnder Plot no 29 Institutional Area Sector 32 Gurugram 122 001 Shift Timings 12 noon to 8 pm
Full Time
Key Skills :
research
...
Job Description:
For the position Senior Research Analyst - Technology and Communications T C Company Egon Zehnder is the worlds leadership consulting advisory f...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Egon Zehnder -
research
associate
- Private Equity Sector
Egon Zehnder -
research
associate
- Private Equity Sector
Egon Zehnder - Knowledge Center India
8-13 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
Egon Zehnder -
research
associate
- Private Equity Sector
12-12-2019
2020-03-11
For the position- Research Associate - Private Equity Practice Company Egon Zehnder is the worlds leadership consulting advisory firm sharing one goal to transform people organizations and the world through great leadership As One Firm our more than 400 Consultants in 69 offices and 41 countries bring our individual strengths to form one powerful collaborative team We partner closely with public and private corporations family-owned enterprises and non-profit and government agencies to provide Board advisory services CEO search and succession executive search executive assessment leadership development and organizational transformation Egon Zehnder Knowledge Center India EZ KCI The Research Team is a group of experts aligned to specific Industry or Functional Practice that works on with global teams in solving client mandates Researchers provide insights from internal external databases expert perspectives on industry trend and through their experiences Most of the team members come with an industry specialization working in consulting or industry or both and deliver insights for solving critical client problems Roles Responsibilities The role is broad based covering business development search assignment execution and knowledge management This is an individual contributor role which requires extensive collaboration and engagement with colleagues in Global office This role will be visible to clients and will be expected to help develop key account strategies Required knowledge experience - 8 years of professional experience in Industry Consulting or Research with deep knowledge of the Private Equity Industry at large its competitive landscape including the very latest trends - Experience of working on international engagements in a professional services environment with an understanding of global market - A self-starter with learning agility engaging remotely thought partnering critical thinking eye for detail conceptual thinking Location Egon Zehnder Plot no 29 Institutional Area Sector 32 Gurugram- 122001
Full Time
Key Skills :
research
, consulting - bfsi...
Job Description:
For the position- Research Associate - Private Equity Practice Company Egon Zehnder is the worlds leadership consulting advisory firm sharing one...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Egon Zehnder -
research
associate
- Financial Services Sector
Egon Zehnder -
research
associate
- Financial Services Sector
Egon Zehnder - Knowledge Center India
9-12 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
Egon Zehnder -
research
associate
- Financial Services Sector
12-12-2019
2020-03-11
For the position Research Associate - Financial Services FS Company Egon Zehnder is the worlds leadership consulting advisory firm sharing one goal to transform people organizations and the world through great leadership As One Firm our more than 400 Consultants in 69 offices and 41 countries bring our individual strengths to form one powerful collaborative team We partner closely with public and private corporations family-owned enterprises and non-profit and government agencies to provide Board advisory services CEO search and succession executive search executive assessment leadership development and organizational transformation Egon Zehnder Knowledge Center India EZ KCI Established in January 2005 KCI in Gurgaon works in close collaboration with the Global offices of Egon Zehnder The Research Team is a group of experts aligned to specific Industry or Functional Practice that works on with global teams in solving client mandates The Researchers provide insights from internal external databases expert perspectives on industry trend and through their experiences Most of the team members come with an industry specialization working in consulting or industry or both and deliver insights for solving critical client problems Roles Responsibilities - The role is broad based covering business development search assignment execution and knowledge management - This is an individual contributor role which requires extensive collaboration and engagement with colleagues in Global office This role will be visible to clients and will be expected to help develop key account strategies Required knowledge experience - 9-12 years years of professional experience in Industry Consulting or Research with deep knowledge of the Financial Industry at large its competitive landscape including the very latest trends - Experience of working on international engagements in a professional services environment with an understanding of Global market - A self-starter with learning agility engaging remotely thought partnering critical thinking eye for detail conceptual thinking
Full Time
Key Skills :
research
, consulting - bfsi...
Job Description:
For the position Research Associate - Financial Services FS Company Egon Zehnder is the worlds leadership consulting advisory firm sharing one ...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
MagicPin -
associate
Product Manager
MagicPin -
associate
Product Manager
MagicPin
2-4 Yrs
15 hrs ago
Gurgaon, Gurugram
Gurgaon
,
Haryana
IN
0
Gurgaon
Gurugram
Not Mentioned
IN
0
Gurugram
MagicPin -
associate
Product Manager
12-12-2019
2020-03-11
About magicpin magicpin is Indias largest retail rewards platform that drives discovery and commerce for offline businesses More than 5M users are hooked on to the app where they spend up to 80 minutes per day We drive 350M of business to merchants on the platform and have grown 5x in the last 12 months with partners ranging from large brands like McDonald- s Beer Caf- Decathlon ITC Emami Pernod Ricards to thousands of local retailers across the country The management team consists of seasoned professionals from Lightspeed VP Nexus VP Bain Co McKinsey Walmart Labs Microsoft Goldman Sachs and educational background including IIT IIM Stanford and SRCC The company has been invested in by Lightspeed Oyo Snapchat Limeroad and Google About us https magicpin in about-us Roles and Responsibilities - Maintain complete ownership of the sales products within the magicpin - Ideate and maintain retail sales product plan with new features enhancements and timelines - Create PRDs agile stories wireframes and establish key performance metrics for new feature and initiatives - Ability to understand technical architecture of product - Ability to handle multiple products at a time - Ensure prioritization timely execution quality resolving issues faced during operationalization and ensuring success metrics are met - Own key metrics define requirements create and deliver on plans through cross functional teams with design tech Knowledge and Skills - Understanding of technology fundamentals successful B2B products - 2 years- experience in B2B B2C product management product analytics is a must - Knowledge of python and Sql is plus - Key traits we seek are passionate ownership collaboration problem solving curiosity imagination being well-read and persistent - Ability to interpret data and make sense without getting stuck in analysis paralysis - Passion for hands-on UX research and process orientation will be a plus - Comfort in operating independently and working in unstructured situations - Understanding of different databases ranging from Rdbms NoSql Redis is a plus - Self-starters with high end to end ownership who can liaise with other teams to create a product with limited past precedent - Excellent written communication skills
Full Time
Key Skills :
it product management, online product management...
Job Description:
About magicpin magicpin is Indias largest retail rewards platform that drives discovery and commerce for offline businesses More than 5M users ar...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Sales Head - FMCG
associate
Sales Head - FMCG
Catalyst Management Consultants
14-20 Yrs
15 hrs ago
Madurai, Coimbatore, Tamil Nadu
Madurai
,
Tamil Nadu
IN
0
Madurai
Coimbatore
,
Tamil Nadu
IN
0
Coimbatore
Tamil Nadu
Not Mentioned
IN
0
Tamil Nadu
associate
Sales Head - FMCG
12-12-2019
2020-03-11
1 Lead and manage the sales operations for the region 2 Supervise a team of 4-5 ASMs and 60 sales officers 3 Would be responsible to manage and drive sales through general trade and modern trade 4 Would be second in line to the Sales Head Desired Candidate 1 The candidate should posses minimum 14 years of experience preferably in the FMCG industry 2 Should be a hard core sales professional with strong operational expertise 3 Should possess very strong leadership qualities and should have managed large team of at least 50 - 60 sales officers 4 Should be conversant in Tamil mandatory English and Hindi
Full Time
Key Skills :
sales, fmcg sales, sales head, general trade, modern trade...
Job Description:
1 Lead and manage the sales operations for the region 2 Supervise a team of 4-5 ASMs and 60 sales officers 3 Would be responsible to manage a...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Global Insights & Analytics Lead - Shared Services Centre - FMCG
Global Insights & Analytics Lead - Shared Services Centre - FMCG
People Connection
8-15 Yrs
15 hrs ago
Mumbai
Mumbai
Maharashtra
IN
0
Mumbai
Global Insights & Analytics Lead - Shared Services Centre - FMCG
12-12-2019
2020-03-11
A leading FMCG company with its shared services centre in Mumbai is looking to hire a Global Insights and Analytics Lead We are looking for candidates specifically with minimum of 8-10 years experience in Syndicated Research Point of sales tracking pricing strategy data etc who have worked on Retail Panel data We are looking for experience in handling Global Data management and analytics multi country experience-This is a MUST Important Candidates with Primary Research experience will not be considered for this role The role will encompass the following 1 Lead a Capability team Segment focused insights team will roll up to this role and the incumbent will be responsible for overall leadership talent development skill advancement engagement and retention of talent on the team 20 people 2 Advance Research skills across the team Foster learning mindset in the teams to advance research and story-telling skills across multiple sources of data to answer business questions 3 Advance new capabilities Partner with Global GIA lead to grow and develop newer capabilities under Global GIA umbrella like Omni-channel new sources of data segment level analysis etc 4 Stakeholder Management in a matrix organisation 5 Identify and elevate cross segment opportunities Leverage global scope of role to identify common projects themes and assist with cross-pollination of best practices and learnings 6 Play a key role on to take the global vision forward Partner across different teams with within Shared Services Centre to advance capabilities collaboration and culture
Full Time
Key Skills :
analytics,
research
, consumer insights, market
research
...
Job Description:
A leading FMCG company with its shared services centre in Mumbai is looking to hire a Global Insights and Analytics Lead We are looking for candida...
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INR
Array
Array
Array-Array
"YEARLY"
associate
Director - Business Operations - Cash Logistics Firm
associate
Director - Business Operations - Cash Logistics Firm
Avant Garde Corporate Services Pvt Ltd
16-18 Yrs
15 hrs ago
Ahmedabad, Mumbai
Ahmedabad
,
Gujarat
IN
0
Ahmedabad
Mumbai
Maharashtra
IN
0
Mumbai
associate
Director - Business Operations - Cash Logistics Firm
12-12-2019
2020-03-11
Responsibilities - Overall Accountability for Regional Operations - Effectively strategizing handling Logistics operations maintenance and route optimization for the assigned region - Identifying managing risk factors during operations Analyzing operations carried out with proper infrastructure like manpower vehicles trunks locks etc - Managing ATMs CDP in the region - Fleet Management Manpower Management - Effectively handle process related improvements - Liaison with government bodies RTO Police and Local Municipal officials etc - Provide efficient and effective customer service to achieve high client satisfaction levels - Conduct Regular Audits - Keeping close watch on process adherence conduction surprise audits Qualifications Skills - Masters degree in operations plus a minimum of 16 years of full-time experience of leading field operations in Logistics or Retail industry - Demonstrates strong verbal and written communication skills - Ability to positively influence behaviors and outcomes guide and influence leadership manage large teams - Excellent time management skills and ability to prioritize - Having keen analytical Problem Solving skills - Goal Orientation - Ability to handle pressure and deadlines - Having high level of integrity and honesty
Full Time
Key Skills :
fleet operations, operations, logistics, logistics head, operations head...
Job Description:
Responsibilities - Overall Accountability for Regional Operations - Effectively strategizing handling Logistics operations maintenance and rout...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Kautilya Finance Investment Advisors -
associate
/
associate
Vice President - Legal - Real Estate PE Fund
Kautilya Finance Investment Advisors -
associate
/
associate
Vice President - Legal - Real Estate PE Fund
Kautilya Finance Investment Advisors
3-5 Yrs
15 hrs ago
Delhi Ncr
Delhi Ncr
Not Mentioned
IN
0
Delhi Ncr
Kautilya Finance Investment Advisors -
associate
/
associate
Vice President - Legal - Real Estate PE Fund
12-12-2019
2020-03-11
The Company Kautilya Finance Investment Advisors LLP KFIA is the Investment Manager of Kautilya Real Estate Fund KREF which is a SEBI registered Category 2 Alternate Investment Fund - AIF- KREF is a real estate debt fund KF has invested Rs 700 crores in Delhi NCR Mumbai and is planning to invest additionally up to Rs 1 100 crores by December 2020 KREF is backed by a variety of domestic as well as international institutional investors Location Delhi NCR Designation Associate Associate Vice President Qualification B A LL B from National Law Schools or from reputed national international colleges Experience 3-5 years in Real Estate Banking Finance Role Kautilya Finance is looking to hire Associate Associate Vice President for the role of the legal team The role is based out of South Delhi The person will be dealing with partners of the top law firms for whom this person will be a client - The person will be responsible for finalizing the term sheet the transaction documents and closing of the transaction - The person will be required to liaise with the external law firms and the borrower for timely finalization and execution of the documents and will also be required to visit the borrowers office to ensure completion and compliance of the conditions precedent conditions subsequent and other covenants of the transaction documents including creation perfection and registration of the security - The end result of the process undertaken by the legal person will be disbursement of monies to the Issuer of NCDs - The main area of work would involve drafting legal documents for extending investments via NCDs bringing in standardization in documentation work overseeing the litigation and recovery function and guiding the team to ensure complete ownership of the legal function of Kautilya Finance - The person will liaise with the external law firms and the borrower for A completion of the title due diligence and corporate due diligence and B finalization and execution of the transaction documents including debenture trust deed escrow agreements and the security agreements - The person will also be responsible for the creation perfection and registration of the security within the timelines agreed in the transaction documents The person will also monitor and strategize transaction structuring due to changes in applicable laws - The ideal person would have worked with a top tier legal firm while drafting debenture trust deeds and security agreements Compensation Will be as per the market standards
Full Time
Key Skills :
llb, legal jobs in bfsi, regulatory compliance, legal jobs in real estate, litigation...
Job Description:
The Company Kautilya Finance Investment Advisors LLP KFIA is the Investment Manager of Kautilya Real Estate Fund KREF which is a SEBI registered...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical
research
Project Manager
Clinical
research
Project Manager
ASTRAZENECA PHARMA INDIA LTD
5-8 Yrs
14 hrs ago
Turkey
Turkey
Not Mentioned
IN
0
Turkey
Clinical
research
Project Manager
12-12-2019
2020-03-11
Background Qualifications University degree preferably from Healthcare related areas Pharmacy Veterinary Chemistry Biology Medical etc Faculties Advanced level of English Minimum 5 year experiences in Clinical Research preferably 2 years in Project Management positions Project management skills Strong communication and negotiation skills Ability to prioritize and handle multiple tasks Basic coaching skills and good at team work Financial management skills Effective planning and organizational skills with result-oriented approach Stakeholder management experience Analytical thinking critical reasoning ability Good command of MS Office applications No restriction to travel Driving License No military obligation for male candidates Summary Leading the local study teams consisting of monitors and study administrators at country level to deliver committed components of clinical studies according to agreed resources budget and timelines Ensuring that study sites are identified site qualifications performed set up initiated monitored closed and documentation archived Ensuring timely submissions of proper application documents to Ethic Committee Regulatory Authority Close communication with global study teams and overall responsibility for study commitments for timely delivery of data to required quality as agreed with global Creating and implementing alternative action plans proactively in order to reach the targeted patient numbers monitoring the patience admission processes in coordination with the researchers planning and taking the necessary precaution when required Ensuring the compliance of the clinical research process with ICH-GCP practices the study protocol AZ Global and Local Clinical SOPs and the Ministry of Health Clinical Research Regulations being knowledgeable about these procedures and keeping abreast of any changes and revision Participating in system process improvement projects within global and local task groups consisting of employees from different units AstraZeneca embraces diversity and equality of opportunity We are committed to building an inclusive and diverse team representing all backgrounds with as wide a range of perspectives as possible and harnessing industry-leading skills We believe that the more inclusive we are the better our work will be We welcome and consider applications to join our team from all qualified candidates regardless of their characteristics We comply with all applicable laws and regulations on non-discrimination in employment and recruitment as well as work authorisation and employment eligibility verification requirements Save for Later
Full Time
Key Skills :
sop, action, team work, documentation, process improvement...
Job Description:
Background Qualifications University degree preferably from Healthcare related areas Pharmacy Veterinary Chemistry Biology Medical etc Facul...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Relationship manager - Bancassurance
associate
Relationship manager - Bancassurance
HDFC Standard Life Co Ltd
1-3 Yrs
14 hrs ago
Kolkata, Mumbai
Kolkata
,
West Bengal
IN
0
Kolkata
Mumbai
Maharashtra
IN
0
Mumbai
associate
Relationship manager - Bancassurance
12-12-2019
2020-03-11
We are Hiring Sales or marketing profile For Associate Relationship manager - Bancassurance HDFC Life co Ltd We are looking to employ a sales-driven and customer-oriented Sales Officer to oversee our sales team and determine the most effective solutions to increase company sales The Sales Officers responsibilities include recommending improvements to current sales strategies informing potential and existing customers of company promotions as well as preparing accurate sales and expense reports You should also be able to continually identify new sales opportunities through customer referrals To be successful as a Sales Officer you should be persuasive and knowledgeable of industry regulations Ultimately an outstanding Sales Officer should have a strong work ethic and demonstrate exceptional communication negotiation and customer service skills at all times Responsibilities Supervise development of credit applications and monitor portfolio of individual unit Coordinate with finance global network and other departments and ensure effective performance Supervise allotted account portfolios and ensure excellent customer service and assist in minimizing of financial risk Prepare management reports for various industry studies and identify appropriate market opportunities Analyze all business objectives and ensure achievement of all product mix for all relationships with customers Analyze clients requirements and manage all client communication and counseling for customers and prepare required documentation Participate in sales planning initiatives and design appropriate relationship plans to generate new business through out-marketing calls promotions and presentations Administer all work and ensure compliance to all guidelines sales process and standards to ensure effective inspections Provide excellent customer service and assist to open new accounts for clients and maintain necessary documents for all operations and maintain effective relationships with clients Assist bankers to arrange credit facility participate in client meeting and prepare marketing materials for new clients and prospective clients Supervise and administer work of ARM s management in loan underwriting loan packages portfolio monitoring and business development Assist relationship manager and portfolio manager in portfolio management credit renewal packages Analyze financial statements of new customer and evaluate all loan documents Maintain knowledge on all bank products credit standards services and trends and provide efficient customer services Participate in various business development calls with senior officials and develop efficient credit proposals and structure for same Coordinate with senior officers in business plan development prepare credit packages and perform credit analysis and provide update for call lists
Full Time
Key Skills :
sales, cross selling, credit card, finance, loan...
Job Description:
We are Hiring Sales or marketing profile For Associate Relationship manager - Bancassurance HDFC Life co Ltd We are looking to employ a sa...
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INR
Array
Array
Array-Array
"YEARLY"
research
Scientist - Analytical
research
Scientist - Analytical
PI Industries Ltd
2-5 Yrs
14 hrs ago
Udaipur
Udaipur
Rajasthan
IN
0
Udaipur
research
Scientist - Analytical
12-12-2019
2020-03-11
The incumbent would provide support to the Process Research team by providing assistance in reaction monitoring on HPLC GC NMR IR LCMS characterization and data generation of submitted compounds final product assay method development Analysis of impurities physical characterizations residue content stability studies etc Strategic Responsibilities Actively imbibing the values and philosophy of PI Industries Efficient contribution to the overall success of CreAgro Analytical Chemistry through scientific contribution and supporting team performance according to objectives and targets being set by the leadership team Remain at the cutting edge of knowledge required for the new a i discovery activity in crop protection through constant updating of personal knowledge and own skill-sets Operational Responsibilities Experimental determination of several phys-chem parameters like Small molecules Aqueous solubility Solubility in different solvents pKa logP Henrys Law constant as per OECD guidelines Strong theoretical back ground on the aforesaid phys-chem parameters Analysis of the phys-chem experimental results using Microsoft Excel and GraphPad Prism Good knowledge of statistical analysis like paired student t-test and others Conducting Photo Stability and hydrolytic stability studies Operational skill in Spectroscopic Chromatographic Techniques Evaluate different equipments required for the work and operation of the same Prepare the Study Strategy and implement as per SOP Documentation and reporting of analytical results Comply to all safety requirements of the role Financial Responsibilities Work with in the limit of budgets Suggest cost improvement areas to the Team Leader Group Leader People Responsibilities Collaborate with team members and cross functional teams to ensure meeting research objectives Ensure team harmony through collaboration and active participation in all team discussion Education Qualification MSc Organic Chemistry Analytical Chemistry Agriculture from a reputed University Institute with excellent academic credentials Work Experience 2-5 years of hands on experience on Assay of a i by potentiometry HPLC GC impurity purification analysis Experience in chromatography method validation is an added advantage Industry to be Hired from Agro Chemical Pharma Generics Research Universities or Institutes Functional Competencies Scientific Knowledge Research Approach Data Analysis Experimental Skills Interaction Complexity and Team Work Interaction Frequency Purpose of Interaction Internal Team Members Group Leader As and when required Planning work discussing results of experiments resolving doubts for hiring and HR related issues for reimbursement claims
Full Time
Key Skills :
group leader, sop, safety, team work, documentation...
Job Description:
The incumbent would provide support to the Process Research team by providing assistance in reaction monitoring on HPLC GC NMR IR LCMS characte...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Senior Study Physician / Study Physician
Senior Study Physician / Study Physician
ASTRAZENECA PHARMA INDIA LTD
2-5 Yrs
14 hrs ago
Poland
Poland
Not Mentioned
IN
0
Poland
Senior Study Physician / Study Physician
12-12-2019
2020-03-11
Currently AstraZeneca AZ seeks a Senior Study Physician Study Physician in Early Clinical Development This individual will help to ensure AZs continued success in these strategic therapeutic areas through innovative research and outstanding scientific leadership The Study Physician will support the planning implementation and daily operation of drug development projects across the cardiovascular renal and metabolic therapeutic areas or respiratory She he will collaborate with key internal and external stakeholders and will be likely to serve as project Medical Monitor on one or more projects The Study Physician will also be supporting Early Clinical Development ECD responsibilities and contributions to internal teams of clinical development professionals program teams and workstreams responsible for delivering Drug Development projects Major Duties and Responsibilities Direct Oversee the design and implementation of early stage clinical projects as a member of the clinical project team Ensure that the overall scientific and medical content of all clinical programs is sound Ensure the integration of pre-clinical and early clinical findings with planned clinical programs work to secure cross functional alignment and or transparent discussion of risks associated with clear plans to further investigate and track through clinical development Support clinical team activities and lead Study Teams and provide expertise and contributions to Clinical Project Teams Study Teams and Global Program Teams which involves responsibilities ensuring delivery of the portfolio of early assets Support or lead cross-functional ad-hoc workstream matrix teams comprised of multidisciplinary professionals and clinical scientists which involves responsibilities ensuring delivery of specific tasks or input needed for efficient delivery of the portfolio of early assets Direct and be responsible for the short and mid-range clinical research efforts and progress by executing clinical study projects and support information flow on key progress reports to senior directors and others assigned to the Project Team as well as Clinical Project and Study Teams on a global basis Prepare clinical development plans and institute properly approved clinical protocols Design scientifically rigorous and maximally cost-effective clinical development program for the desired indication s Present and defend study protocols Implement clinical R D policies SOPs and related directives Monitor study progress leading the analyses and data evaluation and analysis process for progress-reporting and presentations to senior management Prepare and deliver clinical content needed for various official and regulatory documents such as Dossiers NDAs INDs Safety and Annual reports handling of responses to regulatory agencies regarding questions about complex safety or efficacy issues Serves as Medical Monitor responsible for the safety monitoring of clinical trials and as medical expert for Phase I-II studies managing the process from protocol development thorough individual study report and integrated regulatory documentation Working with Patient Safety ensure that Serious Adverse Events are properly reported on a global basis Support any needed due diligence and prepare present medically sound strategy and plans associated with advanced business development opportunities Contribute and support Department Clinical initiatives to improve the quality and content of all clinical programs as well as the cross functional organization processes designed to effectively deliver our R D portfolio Requirements Qualifications Prior experience in clinical research design implementation of protocols review interpretation of data is required This could be obtained through prior work in the pharmaceutical industry Regulatory or academic clinical research Must demonstrate knowledge of the clinical development process and have direct clinical research and experience Knowledge of clinical trial management data management and drug development process A detailed understanding of human disease pharmacology biochemical medicine and the relevance of pharmacodynamic clinical endpoints that underlie the action of the drug s being developed Must demonstrate up-to-date scientific knowledge in main area of clinical interest Team leadership experience preferred Education MD with a valid medical license required Medical specialty and sub-specialty fellowship training and certification are required within cardiovascular renal and metabolic therapeutic areas or respiratory or similar qualifications from pharma-industry
Full Time
Key Skills :
pharmaceutical industry, data management, regulatory, regulatory documents,
research
...
Job Description:
Currently AstraZeneca AZ seeks a Senior Study Physician Study Physician in Early Clinical Development This individual will help to ensure AZs co...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Prepared Food II Cafe
associate
Prepared Food II Cafe
associate
WALMART INDIA
3-5 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Prepared Food II Cafe
associate
12-12-2019
2020-03-11
What youll do at Provides high quality Member service by acknowledging the Member identifying their needs assisting with purchasing decisions locating merchandise resolving issues and concerns promoting the Companys products and services operating hardware such as cash registers or related equipment processing member purchases assisting in payments returns refunds and exchanges maintaining Prepared Foods CafC operations in accordance with Company policies and procedures to exceed member expectations preparing Cafe food using proper equipment ensuring machines and equipment are properly functioning stocking supplies and products to meet Member needs and using appropriate procedures for different membership and payment types Maintains the Prepared Foods CafC area in accordance with Company policies and procedures by properly handling claims and returns zoning the area arranging and organizing merchandise cleaning the Prepared Foods CafC area for example windows mirrors display cases coolers utilizing approved chemicals supplies tools and equipment and identifying shrink damages or quality issues Maintains safety of Facility by following all safety standards procedures and guidelines including conducting safety sweeps following proper forklift spotting procedures following proper procedures for handling and disposing of hazardous materials following Company steel standard guidelines and correcting reporting unsafe situations to Management Maintains merchandise presentation by receiving and stocking merchandise setting up and cleaning organizing product displays removing damaged goods signing and pricing merchandise appropriately completing paperwork logs and other required documentation following Company policies and procedures for preparing handling packaging labeling and storing food utilizing operating and sanitizing food-related equipment stocking and displaying food products maintaining and cleaning the Prepared Foods CafC area and securing fragile and high-shrink merchandise Minimum Qualifications Outlined below are the required minimum qualifications for this position If none are listed there are no minimum qualifications Minimum Qualifications I acknowledge that the position for which I am applying requires me to successfully complete all job required trainings and assessments within a prescribed time period if I receive the position Must be 18 years of age or older Preferred Qualifications Outlined below are the optional preferred qualifications for this position If none are listed there are no preferred qualifications Supervising Associates Food Services - ServSafe Certification - Certification Minimum Qualifications Minimum Qualifications English language Proficiency Comprehending Reading Speaking Writing I acknowledge that the position for which I am applying requires me to successfully complete all job required trainings and assessments within a prescribed time period if I receive the position About Sams Club Sam Walton opened the first Sams Club in 1983 to meet a growing need among customers who wanted to buy merchandise in bulk Since then Sams Club has grown rapidly opening more than 600 clubs in the U S and 100 clubs internationally By offering affordable wholesale merchandise to members Sams Club helps make saving simple for families and small business owners Sams Club employs about 110 000 associates in the U S The average club is 134 000 square feet and offers bulk groceries and general merchandise Most clubs also have specialty services such as a pharmacy an optical department a photo center or a tire and battery center
Full Time
Key Skills :
forklift, documentation, safety standards, safety...
Job Description:
What youll do at Provides high quality Member service by acknowledging the Member identifying their needs assisting with purchasing decisions locat...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
research
Scientist Chemistry
research
Scientist Chemistry
PI Industries Ltd
1-7 Yrs
14 hrs ago
Udaipur
Udaipur
Rajasthan
IN
0
Udaipur
research
Scientist Chemistry
12-12-2019
2020-03-11
Position Description Business Division CreAgro Department Chemistry Location Udaipur Position Title- Research Scientist - Chemistry Reporting to Title Group Leader Chemistry Level E1 E4 Position Purpose The role holder shall report to the Group Leader and shall perform research activities as designing and conducting scientific experiments analyzing and interpreting results leading to the discovery and pre-development of innovative molecules for crop protection crop growth with the aim of adding significant value to the business of PI Strategic Responsibilities Actively imbibing the values and philosophy of PI Industries Efficient contribution to the overall success of CreAgro Chemistry by driving innovation and team performance according to objectives and targets being set by the Director and Head of Chemistry Fullfilling requirements as set by Group Leader and Team Leader e g within specific Research Projects Ensuring the security of intellectual property for CreAgro patent applications ensuring freedom-to-operate Updating self with respect to chemistry knowledge through literature scanning to foster innovation Support the Team Leader with special focus on target setting and constantly seek functional feedback Operational Responsibilities Work with the Team to achieve and exceed targets within the frame given by the Group Leader and Team Leader Continuous documentation and reporting of all research results obtained within the area of responsibility Carrying out literature search by use of available tools Reaxis Scifinder Patents etc Carrying out synthetic experiments safely efficiently capturing all the experimental procedures and data effectively Update on the functional progress issues of the project on a regular basis and actively seek functional support from Team Leader Constructive and active participation in all technical and functional meetings of the Team Responsible for individual safety Financial Responsibilities People Responsibilities Foster an environment of knowledge sharing within the Team Maintain healthy working relationships with the related teams and departments in CreAgro Education Qualification MSc PhD in Organic Analytical Chemistry from a reputed University Institute from India or overseas with excellent academic credentials Post-doctoral research experience in a reputed university is preferred Work Experience Good experimentalist with experience in industry for 1-7 years Experience of working in discovery process development chemistry Industry to be Hired from Agrochemical Fine Chemical Pharmaceutical Functional Competencies Scientific Knowledge Research Approach Data Analysis Experimentation Skills Interaction Complexity and Team Work Internal Other Chemistry Analytical Chemistry Team members Biology SCM Team Other support functions External Chemical Logistics Service Engineers
Full Time
Key Skills :
innovation, team work, documentation, group leader, safety...
Job Description:
Position Description Business Division CreAgro Department Chemistry Location Udaipur Position Title- Research Scientist - Chemistry Report...
Apply Now
INR
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"YEARLY"
Clinical Science Program Manager
Clinical Science Program Manager
STRYKER INDIA
5-8 Yrs
14 hrs ago
Gurgaon
Gurgaon
Haryana
IN
0
Gurgaon
Clinical Science Program Manager
12-12-2019
2020-03-11
Stryker is one of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care The Company offers a diverse array of innovative medical technologies including reconstructive medical and surgical and neurotechnology and spine products to help people lead more active and more satisfying lives We are currently seeking a Clinical Medical Affairs Program Manager to join our Neurovascular Division to be in Fremont CA or remotely anywhere in the US Strykers Neurovascular division is focused on advancing the practice of less invasive stroke therapies through its Complete Stroke Care solutions The business is dedicated to providing innovative stroke products and services for ischemic and hemorrhagic stroke and committed to providing clinical education and support to help physicians deliver better patient outcomes Products include stent retrievers detachable coils stents balloons guidewires and microcatheters In February 2019 Stryker Corporation NYSE SYK announced that for the ninth consecutive year has been named as one of the 2016 FORTUNE 100 Best Companies to Work For ranking 11 out of 100 If you join our organization will be working to Make Stroke History Stroke is devastating 1 of 20 deaths is from a stroke according to the CDC Watch this video to see how Stryker is making a difference https www youtube com watchv JANFZrpt1Hg Who we want A scientific mindset Has a scientific approach to medical questions and can effectively discuss complex information A critical thinker Can competently evaluate interpret and analyze complex information and data A medical writer Excellent evidence-based medical content creator with superior medical writing skills A communicator Thrives in a cross-functional environment communicating with teams across the organization A team player Dependable collaborative player who puts team success first What you will do As a Clinical Science Program Manager you will be working to Make Stroke History Stroke is devastating 1 of 20 deaths is from a stroke according to the CDC As a Clinical Scientist and a Medical Writer you will make sure our devices have sufficient clinical evidence to place and keep them on the market You will work directly with study investigators and regulatory agencies You will use product knowledge and quick thinking to solve problems and will collaborate with regulatory teams on all phases of regulatory submissions and approvals including clinical document preparation formulation of responses to regulatory agencies and other regulatory documentation You will drive a culture of continuous improvement in the Clinical Evidence Report CER medical writing processes You will also collaborate cross-functionally to provide a CER strategy and develop strong CERs and related clinical regulatory documentation incorporate new update regulatory requirements execute on critical strategic projects for publication reimbursement or indication expansion You will represent Stryker Neurovascular as the subject matter expert within department for the Global product portfolio developing and maintaining in-depth therapeutic and product operation knowledge Your main job responsibilities are Serves as medical writing lead on clinical regulatory documents such as those associated with filings and dossiers including writing and maintaining Clinical Evaluation Reports Works closely with the Clinical and Regulatory team s on document strategies Converts relevant data and information into a form that meets clinical regulatory document requirements Explains data in manner consistent with the target audience s journal congress requirements and or clinical regulatory requirements Coordinates the review approval and other appropriate functions involved in the production of scientific publishing or clinical regulatory projects Collaborates writing reviewing editing and approval with clinical R D quality assurance safety regulatory and marketing teams on clinical study reports clinical evidence gap assessments marketing collaterals PMCF reports and other documents that require the evaluation of clinical data and or clinical literature Performs literature searches as needed for drafting document content Interprets literature information and makes recommendations for application to scientific publications or clinical regulatory documents Understands assimilates and interprets sources of information with appropriate guidance direction from product teams and or authors Interprets and explains data generated from a variety of sources including internal external studies research documentation charts graphs and tables What you need MS or PhD in engineering biological or life sciences or Masters in Public Health PMP PgMP preferred 5-8 years of progressively increasing responsibility in clinical medical writing or scientific field Medical device industry experience strongly preferred Experience of team management preferred Demonstrated understanding of laws regulations standards and guidance governing the conduct of global clinical studies as well as preparation of clinical documentation in support of regulatory submissions Direct experience with medical and or scientific writing within a medical device industry or related industry including preparation of Clinical evaluation reports and post market surveillance reporting Applied knowledge of project management tools Demonstrated success in a team-based environment Demonstrated interpersonal written and oral communication skills Work From Home Not available Travel Percentage 20 PERCENT
Full Time
Key Skills :
medical writing, regulatory documents,
research
, regulatory requirements, clinical data...
Job Description:
Stryker is one of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficie...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Study Delivery
associate
Study Delivery
associate
ASTRAZENECA PHARMA INDIA LTD
0-3 Yrs
14 hrs ago
Canada
Canada
Not Mentioned
IN
0
Canada
Study Delivery
associate
12-12-2019
2020-03-11
About AstraZeneca At AstraZeneca we are united by a common purpose to push the boundaries of science to deliver life-changing medicines This purpose underpins everything we do our work helps to make hearts healthier to help people breathe easier and to help more people survive cancer Every single day we make a difference by delivering potentially life-changing medicines to millions of people worldwide and by leading breakthrough science that promises to transform the treatment of disease Our purpose is bold and so is our approach Becoming a more agile and innovative company means building a dynamic inspiring culture where we celebrate entrepreneurial thinking and act with a sense of urgency We are courageous taking smart risks and learning from both success and failure We are curious creative and open to new ideas and ways of working Above all we are passionate about science and driven to always put patients first Join us and be part of a great place to work an environment that energizes and empowers each of us to achieve our goal to develop and deliver life-changing medicines Position Title Study Delivery Associate Position Type Full-time Contract - 12 Months Career Level C Location Mississauga Ontario Are you highly organized and take pride in your attention to detail Are you passionate about a career that brings new medicines to patients Do you easily build positive relationships with people and have an affinity for following process The Study Delivery Associate is a member of the extended Local study team and supports the successful delivery of Local and Global studies and projects Your responsibilities include You will actively and effectively deliver study activities to ensure quality compliance and consistency of deliverables to time cost and quality objectives You will build and maintain effective professional relationships with the your team and external investigative site staff You act as the primary contact for clinical supply matters ethics regulatory documentation requirements and payments to both internal and external customers You approve sites for drug shipment You prepare execute track collect review and assess clinical documents and ensure their completeness You review the study scope and design in order to provide input into the site level activation and risk mitigation plan and resolve study related issues or problems You assist the study lead by reviewing and contributing to the development and preparation of all study site level documents as required You support the study regulatory and ethics submission process You lead ethics and regulatory documents for site renewals You ensure audit readiness by conducting quality checks of study documents according to the study Quality Control Plan You plan and compile the appendices for the Clinical Study Report You develop training material and train site personnel your team research monitors etc on study-specific clinical supply and documentation matters as needed You assist with the vendor selection and management process where appropriate You set-up populate update and accurately maintain information in AstraZeneca clinical systems Study Drug Non- Drug Supplies Responsibilities You lead non-drug supplies by developing providing input sourcing ordering approving and initiating the shipment tracking reviewing stock level and approving materials for destruction You prepare and execute Statement of Work SOW and own the activities with vendor for local drug management You collaborate with Global Investigational Product Supplies units to ensure flawless delivery of clinical drug supplies You collaborate and communicate with global study teams and local regulatory contacts to assess Canadian requirements for comparator and or rescue medication and source from local providers if required You review discuss and communicate packaging and labelling requirements as defined by the protocol with vendors You are responsible for the notification investigation and resolution of product quality complaints
Full Time
Key Skills :
regulatory, regulatory documents,
research
, clinical study, clinical documents...
Job Description:
About AstraZeneca At AstraZeneca we are united by a common purpose to push the boundaries of science to deliver life-changing medicines This purp...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Mechanical Design Engineer
Mechanical Design Engineer
STRYKER INDIA
0-3 Yrs
14 hrs ago
Ireland
Ireland
Not Mentioned
IN
0
Ireland
Mechanical Design Engineer
12-12-2019
2020-03-11
Designs develops refines and evaluates mechanical components assemblies or subsystems for electro-mechanical medical devices Uses concurrent engineering and rapid prototyping techniques to reduce product time whilst adhering to deadlines and product costs Provide post market design and product application support for a wide range of medical devices performing engineering analysis and providing product expertise to Operations and QA RA teams for reliability improvement risk management cost reduction and CAPA activities Execute product development projects and work on technical aspects of product commercialization Key Areas of Responsibility Working within the Change Control Process will provide design support to Engineering Change Requests including manufacturing process changes product improvements Supplier Change Requests Supplier Transfers and Supplier PPAP Participate in CAPA projects working closely with cross functional teams including Manufacturing Engineering and Quality Engineering to identify and remediate product quality and process issues Provide design and product application support for operations engineering cost reduction projects Assist end customers in resolving product related issues through problem solving and troubleshooting product designs and product training Support investigation and root cause analysis of customer complaints and field returns using engineering analysis techniques and problem solving methodologies Evaluate and optimize concepts for mechanical function and manufacturability Develop product designs and create prototypes from customer concepts and or specs to test and validate ideas Work with a highly creative design team to invent and develop innovative new product concepts Create smart innovative solutions to mechanical design challenges Conducts research in problem areas of considerable scope and complexity Determine and implement design approaches and parameters and conduct feasibility studies on new designs Will analyze equipment to establish operating data conduct experimental tests and evaluate the results Lead and or participate in design review meetings Select components and equipment based on analysis of specifications reliability and regulatory requirements Work with advanced quality engineers to develop component specific testing and inspection protocols Liaise with advanced process development and supply chain personnel for the specification and sourcing of raw materials and suppliers Communicate with suppliers advanced manufacturing engineering and advanced operations to resolve issues and optimize design for manufacturability and efficiency Will ensure designs are cost efficient manufacturable and reliable Lead and contribute significantly in efforts to determine product requirements generate production drawings for parts and assemblies and develop and manage full product design documentation This position is accountable for achieving product performance and quality objectives and effective execution as well as communicating project status and escalating issues when appropriate Qualifications Knowledge Skills Bachelor of Engineering Degree Mechanical Engineering Manufacturing Engineering Biomedical Engineering Electrical Engineering or Materials Science Excellent interpersonal skills - able to express ideas and collaborate effectively with multidisciplinary teams Open minded- able to recognize good ideas Innovative thinker - able to envision new and better ways to do things Execute problem solving techniques related to design technical issues Good instincts and sound judgment for mechanical and structural design Good understanding of statistical tools and validation verification techniques Excellent analytical skills ability to plan organize and implement multiple concurrent tasks Must be able to analyze and correct product and or process issues and make decisions using independent judgement Ideally has good knowledge of human anatomy and common surgical procedures Good working knowledge of CAM CAE computer systems engineering materials and design coating technologies plastic part design and manufacturing technologies Fluent in 3D CAD with good working knowledge of Finite Element Analysis tools Must be able to read and interpret complex engineering drawings and have a good understanding of geometrical dimensioning and tolerancing Must have the ability to work with and assemble small objects and component parts Ability to operate small hand tools and inspection equipment Must be able to generate follow and explain detailed proposals and operating procedures with an in depth understanding of ISO 13485 and FDA quality system requirements PC Literate word processing spreadsheets data base and strong knowledge of project Management tools is essential Willingness to travel internationally for live surgery visits and global partner collaboration
Full Time
Key Skills :
manufacturing, product engineering, part design, cost reduction, documentation...
Job Description:
Designs develops refines and evaluates mechanical components assemblies or subsystems for electro-mechanical medical devices Uses concurrent engine...
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INR
Array
Array
Array-Array
"YEARLY"
Sales Processing
associate
Sales Processing
associate
HP ENTERPRISE SERVICES
2-5 Yrs
14 hrs ago
Chennai
Chennai
Tamil Nadu
IN
0
Chennai
Sales Processing
associate
12-12-2019
2020-03-11
At Hewlett Packard Enterprise we bring together the brightest minds to create breakthrough technology solutions that advance the way people live and work What sets us apart Our people and our relentless dedication to helping our customers make their mark on the world We are a team of doers dreamers and visionaries inspired by our purpose and driven by our strategy We live by our three values partner innovate and act Our legacy inspires us as we forge ahead always pushing to discover whats next Every day is a new opportunity to advance and grow ourselves our company and the industry Some people call it an obsession we call it a way of life Primary Location Chennai Tamil Nadu Job Category Sales Operations Schedule Full time Shift No shift premium India Hewlett Packard Enterprise advances the way people live and work We bring together the brightest minds to create breakthrough technology solutions helping our customers make their mark on the world Our new innovative IT services organization is HPE PointNext We have the expertise to advise integrate and accelerate our customers outcomes from their digital transformation Responsibilities Performs routine tasks under general supervision in support of sales processing Demonstrates capability in at least one of the following sales processing areas pricing and creating quotes for less- to moderately-complex deals registering information and producing documentation order execution billing and invoice production configuration of order systems according to process standards Enters and checks data for completeness in electronic and paper sales processing and documentation systems identifies and routes incomplete information to senior staffers for resolution Generates standard reports documents and dashboard information refreshes implements changes and updates to reports forms and processes as directed Knowledge and Skills Clerical and administrative skills including data entry proofreading advanced filing and document management Proficient with standard word processing spreadsheet and presentation packages Developing expertise with electronic sales documentation order management and bid and quote systems and tools including standard report generation and data search Understanding of basic order processes systems configurations and documentation requirements Written and verbal communication skills mastery in local language and moderate to high proficiency in English Ability to effectively communicate issues and request resolution from more senior staff If you are Good at partnering innovating and making things happen You are aligned to our core values Holding a Bachelors Degree Having 2-5 years of relevant experience Excellent in verbal and written communication Join us and make your mark We offer A competitive salary and extensive social benefits Diverse and dynamic work environment Work-life balance and support for career development An amazing life inside the element Want to know more about it Then lets stay connected https www facebook com HPECareers https twitter com HPE Careers 1056959 HPE is an equal opportunity employer Female Minority Individual with Disabilities Protected Veteran Status
Full Time
Key Skills :
report generation, word processing, clerical...
Job Description:
At Hewlett Packard Enterprise we bring together the brightest minds to create breakthrough technology solutions that advance the way people live and ...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
IS-Senior
associate
IS-Senior
associate
Morgan Stanley Pvt Ltd
0-3 Yrs
14 hrs ago
Mumbai
Mumbai
Maharashtra
IN
0
Mumbai
IS-Senior
associate
12-12-2019
2020-03-11
IS-Senior Associate - Asia Primary Location Non-Japan Asia-India-Maharashtra-Mumbai MSA Education Level Masters Degree Job Fund Services Employment Type Full Time Job Level Senior Associate Description Job Purpose Morgan Stanley Fund Services is committed to providing the highest standard of services to the funds that we administer Investor Services lies at the heart of this commitment The global Investor Services team is charged with providing a best in class service to both our clients and their investors The Advantage Services team plays a key role in meeting this goal by providing support services to our processing centres in Westchester and Dublin MSAS play a key role in the initial processing of investor information This includes The distribution of Offering Memorandum to potential investors The receipt and review of completed subscription documentation This includes Completion of initial AML review Initial review of subscription documentation for completeness Email communication to investors seeking additional information where required Email communication to investors in response to routine queries The receipt and review of other investor transactions Redemptions transfers etc The setup on investor accounts on FSID The entry of investor transactions into FSID The role of the Manager is key to the delivery of these services Responsibilities of a Manager include Day to day supervision of the Investor Services team Providing a point of escalation and training for the Investor Services team Keeping management in Mumbai Westchester and Dublin appraised of operational issues in a timely manner Providing an effective daily hand over of processing between Mumbai and the other processing centres currently in Westchester and Dublin Participate in global projects including system enhancements and data conversions Principle Accountabilities Service Delivery Monitor the receipt of client and investor information through fax and email Ensure that all investor activity is processed in a timely and accurate manner Ensure that all follow up queries to investors are handled in an appropriate manner Handle routine email and fax queries from investors and fund managers in a professional and prompt manner escalating where appropriate Ensuring that the records of the fund are maintained in a complete and organised manner Produce MIS and other internal operational reports that assist in the effective operation of the team Providing a point of escalation and training for the Investor Services team Keep management in Mumbai Westchester and Dublin appraised of operational issues Providing an effective daily hand over of processing between Mumbai and the other processing centres currently in Westchester and Dublin All of the above should be carried out in compliance with the Service Level Agreements agreed with each client Team Leadership A Manager in Investor Services plays a key role in the day-to-day operation of our team Key responsibilities include Training and mentoring of individual team members and Team Leaders Ensuring that individual team members are aware of the policies controls and procedures that apply to their role Providing an escalation point for team members Ensuring that line management are made aware of any issues in a timely manner Ensuring that the team has appropriate cover in place to cope with annual leave and illness Develop and maintain rapport with peers colleagues and offshore counterparts Conducting regular team meetings and one to one with the team Highlighting resource constraints to line management Compliance Investor servicing requires compliance with a range of policies The Manager should have A detailed knowledge of the offering documentation for the funds being serviced A thorough knowledge of the regulations that pertain to the domicile of the fund being serviced A thorough knowledge of our internal policies and procedures Particular emphasis is required on all matters relating to Anti-Money laundering controls
Full Time
Key Skills :
production, surface modeling, nx, catia, instruments...
Job Description:
IS-Senior Associate - Asia Primary Location Non-Japan Asia-India-Maharashtra-Mumbai MSA Education Level Masters Degree Job Fund Services E...
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INR
Array
Array
Array-Array
"YEARLY"
associate
Underwriter
associate
Underwriter
First American Financial Corporation Ltd.
2-5 Yrs
14 hrs ago
Canada
Canada
Not Mentioned
IN
0
Canada
associate
Underwriter
12-12-2019
2020-03-11
Company Summary Join our team As a global leader in providing title settlement services and risk solutions for real estate transactions First American Title Company NYSE FAF is an ideal place to build your career We have been entrusted with helping our customers achieve and protect their dream of homeownership since 1889 First American Titles National Commercial Services division provides single-point service for simple to multi-property multi-state national commercial real estate transactions We believe that our people are the key to the companys continued success Because our employees enable our future we invest in theirs by supporting their careers and promoting their overall wellbeing First American has created an award-winning culture and has been named to the Fortune 100 Best Companies to Work For 2018 list for the third consecutive year and to more than 50 regional Best Places to Work lists For more information visit www firstam com Job Summary First American National Commercial Services is currently seeking an Associate UCC Underwriter for its Santa Ana CA office Job Summary The primary responsibility of an Underwriter will be to review and analyze Secured Personal Property Transactions under Article 9 of the Uniform Commercial Code and prepare UCC Commitments and Policies for distribution to clients Underwriters will also review and analyze UCC search results and financing statements They will become proficient in reviewing loan documentation including Security Agreements Control Agreements Deposit Accounts Agreements Intercreditor Agreements Interest Rate Caps Corporate documentation and Certificated Securities among others Requirements -College degree preferred -Must possess strong written and verbal communication skills as well as strong attention to detail -Must also be able to multitask and maintain strong attention to detail -Must be Proficient in MS Office and Adobe Acrobat -Must be able to embrace a customer first attitude Preferred -2 years background in banking or finance related to personal property secured transactions under Article 9 of the Uniform Commercial Code -Previous experience with preparing and or reviewing documents such as corporate LLC or partnership agreements resolutions and security agreements
Full Time
Key Skills :
financing, accounts, ca, finance...
Job Description:
Company Summary Join our team As a global leader in providing title settlement services and risk solutions for real estate transactions First Ame...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Watson Health Clinical Affairs Director
Watson Health Clinical Affairs Director
IBM India Pvt Ltd
15-18 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Watson Health Clinical Affairs Director
12-12-2019
2020-03-11
At IBM work is more than a job - its a calling To build To design To code To consult To think along with clients and sell To make markets To invent To collaborate Not just to do something better but to attempt things youve never thought possible To lead in this new era of technology and solve some of the worlds most challenging problems This role will be in our Hartland WI or Cambridge MA site or Remote As a member of the Watson Health RAQA Organization you will provide clinical study leadership strategic guidance and support for new and existing products This role will be a dual role to design and execute clinical research programs to enable successful completion to clinical endpoints as well as supporting the regulatory registration of medical devices requiring clinical data and evidence for the domestic and international market The individual will be involved in the design conduct data management and interpretation and reporting of clinical trials This role will require coordinated development of clinical study strategies with Design teams and Offering Management This individual must ensure that all clinical studies operate to the highest ethical and safety standards and in compliance with company GCP and regulatory requirements Job duties Leads the preparation of study documentation such as clinical plans protocols amendments case report forms investigators brochures study agreements and study reports Contributes to the development of internal standard operating procedures and work instructions Manages and ensures accuracy of regulatory notices and submissions e g clinicaltrials gov Investigational plans Investigators manual and study reports Collects and processes regulatory documents and correspondence Manages and ensures accuracy for MV studies on clinicaltrials gov Coordinates other responsibilities for the Clinical Research Department with other functions Essential Job Duties Develop clinical study designs and reports for clinical studies Review and approve clinical study protocols and other documentation in support of clinical studies Manage US and international regulatory submissions for the conduct of clinical studies and the approval clearance of new products Manage CRO and or other outside clinical study vendors Manage study timelines and budgets Drive clinical study communication to cross-functional teams Support data analysis and interpretation of clinical information Manage the process to compile and summarize post market clinical information to support regulatory documentation Support other clinical activities within the department as needed including tasks in support of IBM-sponsored clinical studies Support staff to submit regulatory applications as well as internal regulatory file documentation to achieve market clearances in US Canada EU Australia Japan and Brazil at a minimum Initiates product holds as needed where market authorizations have not been achieved Acts as a core team member on development teams providing clinical affairs feedback and guidance throughout the product development cycle Reviews and signs-off on product manufacturing changes for compliance with applicable regulations and guidances in US Canada EU Brazil Japan and Australia at a minimum Collaborates with regional business partners to support international product registrations Assists with the development of regulatory department policy and procedure implementation Reviews device labeling and promotional materials for compliance with global submissions and applicable regulations analyzes appropriate changes in accordance with US Canada EU Brazil Japan and Australia regulations at a minimum Performs all duties and responsibilities as required by the Quality Management System Policies and Procedures Assists with activities related to the corrective and preventative action CAPA process Participates in FDA notified body and other regulatory inspections Build quality into all aspects of their work by maintaining compliance to all quality requirements Must be experienced in the medical device quality system regulations and international regulatory requirements for medical devices Specific experience with clinical study design and medical devices desired Bachelors degree in a scientific or health discipline required advanced degree preferred Minimum of 15 years in the medical industry in Clinical Affairs Clinical and Regulatory Proficient in Good Clinical Practices requirements for US and EU Proficient in preparing various types of regulatory submissions including 510 k EU Technical Files Australia technical files Experience with Health Canada Medical Device Licenses and US FDA PMA experience preferred Working knowledge of FDA EU Japan Australia Brazil and Canada as well as other international regulations General understanding of product development process and design control n a IBM Watson Health is pioneering a new partnership between humanity and technology with the goal of transforming global health and revolutionizing many aspects of the medical and pharmaceutical industries as well as government sectors We aspire to improve lives and give hope by delivering innovation to address the worlds most pressing health challenges through data and artificial intelligence insights What matters to you when youre looking for your next career challenge Maybe you want to get involved in work that really changes the world What about somewhere with incredible and diverse career and development opportunities where you can truly discover your passion Are you looking for a culture of openness collaboration and trust where everyone has a voice What about all of these If so then IBM could be your next career challenge Join us not to do something better but to attempt things you never thought possible Impact Inclusion Infinite Experiences Do your best work ever IBMs greatest invention is the IBMer We believe that progress is made through progressive thinking progressive leadership progressive policy and progressive action IBMers believe that the application of intelligence reason and science can improve business society and the human condition Restlessly reinventing since 1911 we are the largest technology and consulting employer in the world with more than 380 000 IBMers serving clients in 170 countries US Citizenship required IBM is committed to creating a diverse environment and is proud to be an equal opportunity employer All qualified applicants will receive consideration for employment without regard to race color religion gender gender identity or expression sexual orientation national origin genetics disability age or veteran status IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status Preferred Education Masters Degree Commissionable No Key Job Details Country US State MULTIPLE City MULTIPLE CITIES Category Enterprise Operations Required Education Bachelors Degree Position Type Professional Employment Type Full-Time Contract Type Regular Req ID 271072BR Location MULTIPLE CITIES MULTIPLE US
Full Time
Key Skills :
regulatory documents, clinical data, regulatory requirements, gcp, clinical trials...
Job Description:
At IBM work is more than a job - its a calling To build To design To code To consult To think along with clients and sell To make markets To i...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Director , Fraud Intelligence and Investigations
associate
Director , Fraud Intelligence and Investigations
Standard Chartered Bank Ltd
0-3 Yrs
14 hrs ago
Bangalore
Bangalore
Karnataka
IN
0
Bangalore
associate
Director , Fraud Intelligence and Investigations
12-12-2019
2020-03-11
Attend and contribute to relevant team and leadership meetings Propose control improvements enhancements and simplifications where appropriate Support senior oversight of FCC region country function In the event of serious regulatory breaches or where risk tolerances have been breached ensure senior management and relevant regulators are informed and that actions are taken quickly to remediate and or activities are ceased Prepare and cascade lessons learned from audit findings FCC assurance activities and specific investigations Regulatory Business Conduct Display exemplary conduct and live by the Groups Values and Code of Conduct Take personal responsibility for embedding the highest standards of ethics including regulatory and business conduct across Standard Chartered Bank This includes understanding and ensuring compliance with in letter and spirit all applicable laws regulations guidelines and the Group Code of Conduct Support the FRM team to achieve the outcomes set out in the Banks Conduct Principles Effectively and collaboratively identify escalate mitigate and resolve risk conduct and compliance matters Key Stakeholders Head FRM Head Fraud Intelligence HRCU colleagues FRM Colleagues I3 Shared Investigative Services Other Responsibilities Embed Here for Good and Groups brand and values in Group i3 Perform other responsibilities assigned under Group Country Business or Functional policies and procedures Leadership and Management Supports efforts to position FRM as an industry leader in the eyes of regulators and industry stakeholders Establishes strong working relationship with key stakeholders across the bank Key Measurables Positive feedback from FRM colleagues the businesses functions regions FCC network senior management regulators and external parties Timely reporting and escalation of significant issues Cross team collaboration Compliance with all SCB policies and procedures Our Ideal Candidate Extensive exposure to complex investigations in financial law enforcement regulatory or professional services Having similar experience and or applicability of experience to Fraud risk and investigations is an advantage Advanced investigative decision making creating Terms of Reference for investigations recording investigations identifying and completing lines of enquiry effectively Good knowledge of IT systems and Bank IT infrastructure would be an added advantage Strong interpersonal skills An ability to get along well with others and to build networks and relationships Excellent communication and business writing skills A proactive attitude to support continued effectiveness and efficiency gains Any degree from a reputed university Relevant fraud qualifications Minimum eight years of relevant experience Apply now to join the Bank for those with big career ambitions To view information on our benefits including our flexible working please visit our career pages
Full Time
Key Skills :
production, enhancements, line management, action, calibration...
Job Description:
Attend and contribute to relevant team and leadership meetings Propose control improvements enhancements and simplifications where appropriate Suppo...
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INR
Array
Array
Array-Array
"YEARLY"
Quality Engineer
associate
Quality Engineer
associate
Goodrich Corporation Ltd
7-10 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Quality Engineer
associate
12-12-2019
2020-03-11
United States of America Location HTX17 Landing Gear - Fort Worth 2901 Northern Cross Blvd Fort Worth TX 76137 USA We are Collins Aerospace and we hope you join us as we REDEFINE AEROSPACE Established in 1934 United Technologies Corp UTC employs over 240 000 individuals and achieves net revenues in excess of 66B Through strategic acquisitions of companies such as Goodrich Hamilton Sundstrand B E Aerospace and Pratt Whitney in recent years the UTC family and its subsidiary companies are positioned become innovation leaders in the Aerospace industry Collins Aerospace was created in 2018 through the combination of two leading companies Rockwell Collins and United Technologies Aerospace Systems UTAS were driving the industry forward through technologically advanced and intelligent solutions for global aerospace and defense Every day we imagine ways to make the skies and the spaces we touch smarter safer and more amazing than ever Together we chart new journeys reunite families protect nations and save lives And we do it all with some of the greatest talent this industry has to offer Collins competitive benefits package includes Medical dental and vision Three weeks of vacation for newly hired employees Generous 401 k plan that includes employer matching funds and separate employer retirement contribution Tuition reimbursement Employee Scholars Program Life and disability coverage Pet New for 2020 Plus discounts on travel hotel Apple products and wireless programs Additional Fort Worth TX site specific benefits include Team building activities Community service participation You could be a great fit for our Quality organization if You take immense satisfaction and pride in the quality of your work Youre the first to point out opportunities for continuous improvement even outside of worknot at all to the annoyance of your friends and family You understand the absolute importance of adhering to complianceall while making your customers proud by achieving a zero-defect quality delivery plan OK We got it You live and breathe Quality So do we For us at Collins Aerospace quality is personal Peoples lives and safety depend on the quality of our products From the child flying for the first time to the men and women who save lives to the astronaut exploring outer space what we do matters every day If you checked the boxes above we invite you to join the Quality organization as we work to be the best aerospace company for the world by delighting our customers with 100 percent on-time delivery and zero defect parts Role Overview This position is for an Entry level Quality Engineering professional Influences process and planning decisions with knowledge and explanations of Quality Engineering policies practices and procedures Ensures that the quality of UTC suppliers products and processes are compliant with internal and regulatory standards and are continuously improving Primary Responsibilities Develops modifies applies and maintains quality evaluation control systems and protocols for materials being processed into partially finished or finished products Working with product design and specification devises testing plans methods and equipment to assure reliability of product Collaborates internally to ensure quality standards are in effect Ensures that projects and process control documentation are compliant with requirements objectives and or contracts Identifies and manages risk in product development primarily utilizing and driving UPPAP core elements e g PFMEA MSA Process Flow and Control Plans etc Develops proactive quality initiative strategies and drives their implementation Performs Escape management procedures root cause analysis and recommends corrective action for design problems for internally produced products processes Ensures all requirements are met for work transfer and process change management including Resourcing Gate and Production Part Approval Process PPAP acceptance Designs and implements product engineering changes to satisfy quality issues raised by customers Responsible for both Program and Product Quality Engineering Responsible for development of new inspection technologies or methodologies to assure product conformance Conducts activities to modify apply and maintain quality evaluation control systems and protocols Provides explanations of testing and inspection plans methods and or technologies to assure reliability and conformance of products and processes Provides analysis and develops recommendations for corrective actions for nonconformities and or design problems for internally produced products processes Utilizes UPPAP core elements e g PFMEA MSA Process Flow and Control Plans etc to identify risk in product development and propose risk management solutions Provides reviews ensure requirements are met for work transfer and process change management including Resourcing Gate and Production Part Approval Process PPAP acceptance Reviews process control documentation to ensure it is in compliance with requirements objectives and or contracts Basic Qualifications This position requires requires a University Degree or equivalent experience and minimum 3 years of prior relevant experience In the absence of a degree 7 years of relevant experience is required This role requires the candidate to be a US Citizen under the current ITAR definition At Collins the paths we pave together lead to limitless possibility And the bonds we form with our customers and with each other propel us all higher again and again United Technologies Corporation is An Equal Opportunity Affirmative Action Employer All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability or veteran status age or any other federally protected class Privacy Policy and Terms Click on this link to read the Policy and Terms Note to candidates regarding interview scams Wed like to make it clear that UTC Aerospace Systems never asks candidates for money If youve been approached with a job offer that you suspect may be fraudulent we strongly recommend you do not respond send money or personal information Please report any suspicious activity to Talent Acquisition
Full Time
Key Skills :
corrective action, safety, rockwell, action, product engineering...
Job Description:
United States of America Location HTX17 Landing Gear - Fort Worth 2901 Northern Cross Blvd Fort Worth TX 76137 USA We are Collins Aerospace and...
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INR
Array
Array
Array-Array
"YEARLY"
Production
associate
1
Production
associate
1
STRYKER INDIA
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Production
associate
1
12-12-2019
2020-03-11
Job Snapshot Employee Type Full-Time Location Salt Lake City UT Job Type Manufacturing Job ID R426752 Assembles standard products per engineering instructions or bill of materials within established times and quality levels Tasks include mechanical assembly electrical assembly gluing and packaging Repairs or reworks products and related sub-assemblies per documentation Inspects products and sub-assemblies for workmanship and compliance to documentation Accurately completes all paperwork relating to jobs performed including work order forms material reject reports inspection reports and stockroom requisition forms Performs tracking system data entry Maintains clean and safe conditions in work area Work From Home Not available Travel Percentage None Stryker Corporation is an equal opportunity employer Qualified applicants will receive consideration for employment without regard to race ethnicity color religion sex gender identity sexual orientation national origin disability or protected veteran status Stryker is an EO employer M F Veteran Disability Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about discussed or disclosed their own pay or the pay of another employee or applicant However employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is a in response to a formal complaint or charge b in furtherance of an investigation proceeding hearing or action including an investigation conducted by the employer or c consistent with the contractors legal duty to furnish information
Full Time
Key Skills :
documentation, mechanical assembly, manufacturing, action...
Job Description:
Job Snapshot Employee Type Full-Time Location Salt Lake City UT Job Type Manufacturing Job ID R426752 Assembles standard products per engin...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Engineer 1: Lab
associate
Engineer 1: Lab
associate
Jacobs Engineering Group Inc.
0-2 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Engineer 1: Lab
associate
12-12-2019
2020-03-11
Engineer 1 Lab Associate - BI 0008SW Description The Buildings Infrastructure Line of Business is a global network of employees which serves both the private and public sector Our employees work to shape the communities we live in by creating world-class projects that transform the future development patterns of those communities We provide our clients award-winning planning engineering architectural and interior design construction and program management and design-build project delivery The Jacobs business model allows us to successfully service our clients leverage our integrated services and provide our employees with growth opportunities while delivering global solutions to our clients local programs We consistently receive high rankings from Engineering News-Record ENR in many classifications including the categories of Top Design Firms Top Contractors Top Green Buildings Design Firms and Top Transportation Companies Job Responsibilities Engineer will report to the site Lab Manager and will be responsible for assuring compliance of materials with specifications standards and codes This position is an entry level role and will work directly with lead engineers over the material testing laboratory as well as the material quality assurance quality control group Responsibilities include functioning as technical leader of material standards on gas utility projects responsible for inter-disciplinary coordination of activities quality control of manufactured materials documentation of finding working with various pieces of equipment to test material structure and conformance with industry and Company requirements Position requires the exercise of discretion and judgment in the coordination of operation Assignments are carried out as directed by a group lead and may include but not be limited to Support the material testing of metals and plastics throughout the lab Accurately document and track findings Works with engineering leads to review specification discrepancies Interfaces with Client technical staff Addresses non-conformance issues identified within materials Perform record search and information gathering Maintain daily reports relative to tasks and quality control items Attend weekly or monthly team project meetings as needed Support analyzing and development of process improvements of work functions Ensure proper documentation for activities that are traceable verifiable complete and accurate Qualifications Job Requirements BS Degree in Engineering required Mechanical or Materials engineer required 0-2 years experience in a professional setting Efficient and effective written and verbal communication skills Must be effective in working both independently and in a team setting Strong organizational skills and time management skills Must be very detail oriented to ensure consistent and accurate results and tracking Pre-employment drug test and background check required Jacobs is an Equal Opportunity Affirmative Action Employer All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability veteran status or other characteristics protected by law Learn more about your rights under Federal EEO laws and supplemental language
Full Time
Key Skills :
action, documentation, planning, utility projects...
Job Description:
Engineer 1 Lab Associate - BI 0008SW Description The Buildings Infrastructure Line of Business is a global network of employees which serves...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
- Client Data Management
associate
- Client Data Management
Morgan Stanley Pvt Ltd
0-3 Yrs
14 hrs ago
Mumbai
Mumbai
Maharashtra
IN
0
Mumbai
associate
- Client Data Management
12-12-2019
2020-03-11
Company Profile Morgan Stanley is a leading global financial services firm providing a wide range of investment banking securities investment management and wealth management services The Firms employees serve clients worldwide including corporations governments and individuals from more than 1 200 offices in 43 countries As a market leader the talent and passion of our people is critical to our success Together we share a common set of values rooted in integrity excellence and strong team ethic Morgan Stanley can provide a superior foundation for building a professional career - a place for people to learn to achieve and grow A philosophy that balances personal lifestyles perspectives and needs is an important part of our culture Team Profile Shared Service Banking Operations SSBO delivers industry utility solutions by aligning the right functions people processes and tools into 14 core disciplines offering tailored client service levels that are efficient controlled and compliant with regulation The Party Referential Data Team is part of the Global Client and Account Data Operations Team CADO within SSBO and is responsible for the creation and maintenance of Morgan Stanley party reference data for clients issuers and vendors for the duration of the entire business relationship The team is located in Glasgow Baltimore and Mumbai and cover requests globally About the Role - Create newly acquired parties client issuer and vendor records in the system This involves investigating various approved sources and analyzing various approved documents to determine key attributes required for operational processing as well as financial and regulatory reporting - Maintain the records of existing parties using the same required analysis and due diligence - Processing Corporate Actions such as name changes mergers etc by validating against approved sources identifying pre- and post-notification requirements of sensitive stakeholders processing the actions ensuring all parties sites hierarchies etc are updated based on the Corporate Action Additionally ensuring all obsolete documents are invalidated and replaced with current valid documentation - Additional duties as they regard party referential data attributes - Partner with key business areas and other stakeholders to assure compliance with policies and regulations as well as to review requests for additional processes and data quality rules which may include remediation initiatives based on new regulations or business requirements - Update proprietary systems with information documentation obtained and potentially performing data quality reviews - Maintain a high level of accuracy and data quality standards Qualifications The ideal candidate will have previous experience knowledge within an Operations related environment They will be a confident analytical person with excellent oral and written communication skills In addition the ideal candidate will possess the following attributes - Qualified at degree level or equivalent industry experience - Aptitude to work in a fast-paced environment - Ability to handle volume spikes and prioritize work including ad-hoc requests and projects to meet business demands in a timely manner - Ability to recognize potential risk issues and escalate report on a timely basis - Adaptability and flexibility ability to perform under pressure or in changing environment - Outstanding attention to details and analytical ability - Proficiency in MS Office Excel PowerPoint and Word - Self-driven capable of performing day-to-day activities with minimal guidance and supervision - Ability to influence stakeholders and gain consensus across different groups
Full Time
Key Skills :
utility, supervision, action, documentation, maintenance...
Job Description:
Company Profile Morgan Stanley is a leading global financial services firm providing a wide range of investment banking securities investment manag...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Pilot Production Technician
Pilot Production Technician
ASTRAZENECA PHARMA INDIA LTD
9-12 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Pilot Production Technician
12-12-2019
2020-03-11
As a pilot production associate in the Clinical production team within Biopharmaceutical Development youll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry In this role you will take an adaptable science driven approach to everything you do You will become an integral part of process development accelerating product candidates into the clinic and gaining knowledge and experience in cell culture purification and critical support activities Under the supervision of highly trained personnel you will gain the process knowledge and skillsets to perform large scale clinical development activities through hands-on training You will join a collaborative and driven team in a world class biopharmaceutical company that is driving disruptive innovation in the industry Qualifications Bachelors degree and 4 years experience OR Associates degree and 5-6 years experience OR high school diploma and 9 years experience Principal Duties Operates production equipment such as bioreactors centrifuges filtration devices chromatography equipment washers autoclaves tanks Weighs and checks raw materials assembles and cleans process equipment monitors processes Performs SIP CIP and manual cleaning and sanitization of equipment Demonstrates aseptic technique Completes production records Maintains clean room environment to comply with regulatory requirements Ensures a safe work environment in accordance with Medimmunes standards Basic understanding of cGMP documentation standards for SOPs MPR and SPRs Adheres to Good Manufacturing Practices and standard operating procedures Regularly works on routine manufacturing assignments Learning and executing basic troubleshooting techniques on equipment and process Works under direct supervision Receives instructions as needed on routine work and more detailed instructions on new assignments Interacts regularly with co-workers senior personnel and supervisor in dynamic and team environment GPF North Principal Duties Operate in a cGMP setting to execute inoculum expansion processes utilizing aseptic technique Set up and operate disposable RM tabletop bioreactors and single use production bioreactors up to 3 x 200L scale Perform purification activities to include column packing column chromatography TFF and bulk fill processes Preparation and filtration of production scale buffer solutions media solutions and weigh and check raw materials
Full Time
Key Skills :
production, production equipment, cip, clean room, sop...
Job Description:
As a pilot production associate in the Clinical production team within Biopharmaceutical Development youll build broad knowledge of bioprocessing in ...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Lead Pilot Production Technician
Lead Pilot Production Technician
ASTRAZENECA PHARMA INDIA LTD
11-14 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Lead Pilot Production Technician
12-12-2019
2020-03-11
As a pilot production associate in the Clinical production team within Biopharmaceutical Development youll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry In this role you will take an adaptable science driven approach to everything you do You will become an integral part of process development accelerating product candidates into the clinic and gaining knowledge and experience in cell culture purification and critical support activities Under the supervision of highly trained personnel you will gain the process knowledge and skillsets to perform large scale clinical development activities through hands-on training You will join a collaborative and driven team in a world class biopharmaceutical company that is driving disruptive innovation in the industry Qualifications Bachelors degree and 6 years experience OR Associates degree and 7-8 years experience OR high school diploma and 11 years experience Principal Duties Assigns daily tasks to more junior production technicians Accurately analyzes and processes scientific data Ensures the completeness and accuracy of manufacturing documentation per approved procedures Reviews Master Production Records for accuracy and completion of process steps Works with more senior manufacturing personnel to improve and optimize manufacturing methods Evaluates operating procedures for accuracy and efficient operation and makes corrections as necessary Serves as the lead investigator for non-conformances as requested Serves as the Subject Matter Expert in area operations Lead unit operation or projects Provides training and operational guidance to more junior staff Serves as the area supervisor when the Supervisor is unavailable Schedules projects in accordance with production timelines as requested Conducts gap analysis on scientific process and develop process improvement plans Purification Technical Principal Duties Perform SIP CIP and ptest on tanks Severs as a SME subject matter expert in Column Chromatography operations TFF Tangential Filtration Flow and column packing Proficient in SAP and pi process book
Full Time
Key Skills :
production, cip, production equipment, supervision, manufacturing...
Job Description:
As a pilot production associate in the Clinical production team within Biopharmaceutical Development youll build broad knowledge of bioprocessing in ...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Attorney Support
associate
Attorney Support
Provana
0-2 Yrs
14 hrs ago
Noida
Noida
Uttar Pradesh
IN
0
Noida
associate
Attorney Support
12-12-2019
2020-03-11
Urgent Opening For Associate Attorney Support Noida 0 - 2 Years Noida Conduct research on relevant laws regulations legal notes articles Investigating the facts of a case Write Reports to help lawyers prepare for trials Draft correspondence and legal documents Note Should be comfortable for rotational shift Keyskills Law Legal Documentation Desired Candidate Profile Please refer to the Job description above Education- UG LLB - Law PG Post Graduation Not Required LLM - Law Company Profile PROVANA INDIA PRIVATE LIMITED Provana India Private Limited Salary INR 2 50 000 - 3 00 000 PA Industry BPO Call Centre ITES Functional Area ITES BPO KPO LPO Customer Service Operations Role Category Voice Role Associate Senior Associate - NonTechnical Employment Type Full Time Permanent
Full Time
Key Skills :
law, legal documentation, legal, lpo...
Job Description:
Urgent Opening For Associate Attorney Support Noida 0 - 2 Years Noida Conduct research on relevant laws regulations legal notes articles In...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Quality Engineer
associate
Quality Engineer
Boehringer Ingelheim India Pvt Ltd
18-21 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
associate
Quality Engineer
12-12-2019
2020-03-11
Leveraging our diverse talent pool we are also driving technology and innovation globally through major investment and collaborations into next generation manufacturing platforms and technologies which may change how biologics will be made in the future Whether we work on our own products help partners to bring their products to market or innovate new technologies and approaches - Everything we do we do to help patients Description The Quality Engineer delivers validation of biopharmaceutical manufacturing equipment utilities computer systems and laboratory instruments and ensures the Engineering and Technology E T department maintains and continuously improves its state of GMP compliance They will be responsible for performing qualification and validation activities in a multi-product biotech manufacturing facility and owning records deviations CAPAs Change Control within the quality systems The BIFI Quality Engineer will develop risk assessments validation plans protocols and reports that support the qualification and validation of systems This individual will be responsible for independently developing simple protocols for small size validation projects using a risk-based approach that meets current regulatory requirements and industry practices They will review and interpret data for accuracy of system performance for completed validations revalidations and prepare final report packages by analyzing and summarizing the data Additionally the BIFI Quality engineer will own Quality System records investigate deviations write investigation reports and create and own CAPAs and change controls This individual will assist in internal customer and regulatory audits by preparing documentation associated with GMP Systems and processes As an employee of Boehringer Ingelheim you will actively contribute to the discovery development and delivery of our products to our patients and customers Our global presence provides opportunity for all employees to collaborate internationally offering visibility and opportunity to directly contribute to the companies success We realize that our strength and competitive advantage lie with our people We support our employees in a number of ways to foster a healthy working environment meaningful work diversity and inclusion mobility networking and work-life balance Our competitive compensation and benefit programs reflect Boehringer Ingelheims high regard for our employees Duties Responsibilities Participate in small size validation Equipment projects Participate with risk assessments for new systems and changes to existing systems Write simple validation plans protocols and reports Owning Quality Systems Records Create own and manage life cycle of minor deviations corrective actions and change controls for GMP equipment facilities and automation systems Operate within the relevant quality computer systems ex SAP TrackWise ensuring implementation in line with quality and timeliness objectives Working closely with Engineering Quality Process Development Validation and Manufacturing to investigate and resolve deviations including leading investigation teams in order to determine root cause product impact and appropriates corrective and preventive actions Preparing material for internal and external regulatory and customer auditors Participate in generating quality system metrics for the E T department Requirements Bachelors Degree from an accredited institution in Engineering with one 1 year of relevant cGMP biopharmaceutical manufacturing environment experience or Masters Degree from an accredited institution in Engineering Working knowledge of GMP guidelines ICH Q7 Q8 Q9 Q10 and other international regulatory requirements Excellent technical writing and verbal communication skills Ability to work as part of a high performing team and collaborate effectively with staff at all levels Must have well-developed interpersonal skills with the ability to establish highly functional relationships with diverse personalities both within and outside the company Demonstrated ability to manage multiple activities while maintaining a high level of organization Preferred experienced in Microsoft Office Suite Knowledge of Microsoft Excel Good knowledge and skills in biopharmaceutical and process engineering Participation on technical projects with an interdisciplinary project team from planning to realization and start up Understanding of validation concepts for biopharmaceutical manufacturing process instrumentation and utility equipment Eligibility Requirements Must be legally authorized to work in the United States without restriction Must be willing to take a drug test and post-offer physical if required Must be 18 years of age or older
Full Time
Key Skills :
instruments, manufacturing, action, instrumentation, documentation...
Job Description:
Leveraging our diverse talent pool we are also driving technology and innovation globally through major investment and collaborations into next gene...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Quality Engineer
Quality Engineer
Electronics for Imaging, Inc
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Quality Engineer
12-12-2019
2020-03-11
Our 3 000 worldwide team members prove our commitment to you every day by developing breakthrough technologies for the manufacturing of signage packaging textiles ceramic tiles and personalized documents with a wide range of printers inks digital front ends and a comprehensive business and production workflow suite that transforms and streamlines the entire production process increasing your competitiveness and boosting productivity EFI is looking for a Quality Engineer to join our Inkjet Solutions Business Unit in our new Manchester NH office near the Airport Develop and implement quality assurance standards processes and controls Develop methods for inspection testing sampling and training Evaluate production capabilities and recommends improvements Provide quality assurance support to ensure that the products produced are manufactured in accordance with the specifications and requirements as defined by the customer and or company Respond to customer identified issues and assist in maintaining the Quality Management System Essential Duties and Responsibilities include the following Other duties may be assigned Ensure and verifies accuracy and completeness of quality requirements inspection sheets engineering documents and sampling sheets used when inspecting parts or units Initiate Corrective and Preventative Action notices as determined necessary to ensure quality processes and products Troubleshoot daily issues and determines the root cause of the problem Initiates proper Problem-Solving procedures to resolve the issue Involves the appropriate departments Document deficiencies identified that do not meet the specifications and requirements Provide a means to track and address repetitive issues Perform required audits by completing necessary inspection procedures product operation certification and test procedures using the appropriate documentation and attesting to the quality of the product prior to shipment Perform reviews of quality acceptance material for produced products evaluate against standards action accordingly Perform product final quality inspections layered process audits and action manage defects with assistance from manufacturing engineering Provide quality standards procedures and controls to assure product quality including design reviews design verification design maturity tests FMEA fault tree analysis MTBF and design of experiments Use basic precision measuring tools workmanship standards visual inspection and referencing specifications and blueprints to identify discrepancies Work with the Field Service Engineering Departments to exchange quality information necessary to promote continuous improvement and customer satisfaction Initiate by completing the information required on the appropriate form pertinent to the Red Tags Rework Sheets issue identified writing Discrepant Material Reports DMR reports and issuing Supplier Corrective Action SCAR reports and needed Perform parts material purge notifications for non-conformances inspect document and implement supplier corrective actions as appropriate Analyze manufacturing and customer warranty returns for parts and products perform root cause analysis request supplier failure analysis and communicate design engineering improvement opportunities to appropriate parties Assist and participate when required and approved by the Quality Manager Effectively use quality tools and techniques to assist in determining compliance with specifications trends capabilities and opportunities for continuous improvement Education Training Bachelors degree in Quality or a related field Three 3 plus years operating in a high-volume manufacturing environment Six Sigma Green Belt certification preferred or willingness to obtain Green Belt certification ASQ member certification a plus Qualifications Skills RCA CAPA FAI 5-Whys Pareto Trend DMAIC 8D Lean Kaizen SPC Knowledge and experience in quality systems Knowledge and experience in quality operations Quality assurance inspection auditing preferred Strong communication skills including effective oral and written abilities at all levels of management employees customers and suppliers Customer first approach to dealing with quality issues and challenges High attention to detail and effective problem-solving skills Proficient computer skills using MS Office Suite with a focus on Excel PowerPoint required SAP Experience a plus Inspiring the world with spectacular imagery
Full Time
Key Skills :
corrective action, manufacturing, mtbf, action, warranty...
Job Description:
Our 3 000 worldwide team members prove our commitment to you every day by developing breakthrough technologies for the manufacturing of signage pack...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Senior service
associate
-Contact Centre
Senior service
associate
-Contact Centre
IBM India Pvt Ltd
1-4 Yrs
14 hrs ago
Hyderabad
Hyderabad
Telangana State
IN
0
Hyderabad
Senior service
associate
-Contact Centre
12-12-2019
2020-03-11
Introduction The HR Service Administrator is an integral part of IBM and HR Your goal is to create an outstanding employee experience for IBMers by delivering HR-related services and supporting our employees as they support our customers and clients Help IBMers to build their career by providing them with a personalized experience In this role you can be part of a team that works with all areas of our global organization and is empowered to achieve goals that align with IBM strategy Your Role and Responsibilities As a Senior service Associate-Contact Centre you are responsible to receive inbound calls from customers and answer questions as well as question Educate callers on client processes whenever necessary Document all calls with regards to callers inquiries accurately using Call Tracking System Bi-hourly and EOD SLA Reports CSAT Scrubbing CSAT VOC VOB KB Gap Analysis Attending forecast and resource planning Calls Critical issue and Supervisor Call Handling Business Controls Reviews validity and completeness of requests Provides data for any internal business controls team as required Ensure compliance to the clients existing standards Implements and follows internal control measures and supports monthly compliance testing to ensure that processes meet business controls requirements Process Documentation Create update and prepare documentation related to processing reports and job aids used to manage data into the HR database If you thrive in a dynamic collaborative workplace IBM provides an environment where you will be challenged and inspired every single day And if you relish the freedom to bring creative thoughtful solutions to the table theres no limit to what you can accomplish here We always believe that it is deeply important to have the right person for the right job and you are a flawless fit to this strategy We want people with an openness and ability to learn and who are ready to put good ideas into action So go ahead and grab the opportunities we wish you outstanding success in your career and inspire you to bring your best self to work with IBM Required Professional and Technical Expertise Minimum 1 Year of experience in Contact Centre Ability to think through complex issues and situations and develop robust well-thought-out solutions which meet the need of the business Demonstrated knowledge to trouble-shoot and implement changes in his her processes ability to identify major areas of concern with compliance to travel policy as well as recommend measures to address identified exceptions ability to analyse and present travel spending data in a way that will provide optimum benefits to the business Preferred Professional and Technical Expertise Ability to liaise with Technology and communicate system requirements You love collaborative environments that use agile methodologies to encourage creative design thinking and find innovative ways to develop with cutting edge technologies Ambitious individual who can work under their own direction towards agreed targets goals and with creative approach to work Intuitive individual with an ability to manage change and proven time management Proven interpersonal skills while contributing to team effort by accomplishing related results as needed Up-to-date technical knowledge by attending educational workshops reviewing publications About Business Unit IBM Services is a team of business strategy and technology consultants that design build and run foundational systems and services that is the backbone of the worlds economy IBM Services partners with the worlds leading companies in over 170 countries to build smarter businesses by reimagining and reinventing through technology with its outcome-focused methodologies industry-leading portfolio and world class research and operations expertise leading to results-driven innovation and enduring excellence Your Life IBM What matters to you when youre looking for your next career challenge Maybe you want to get involved in work that really changes the world What about somewhere with incredible and diverse career and development opportunities where you can truly discover your passion Are you looking for a culture of openness collaboration and trust where everyone has a voice What about all of these If so then IBM could be your next career challenge Join us not to do something better but to attempt things you never thought possible Impact Inclusion Infinite Experiences Do your best work ever About IBM IBMs greatest invention is the IBMer We believe that progress is made through progressive thinking progressive leadership progressive policy and progressive action IBMers believe that the application of intelligence reason and science can improve business society and the human condition Restlessly reinventing since 1911 we are the largest technology and consulting employer in the world with more than 380 000 IBMers serving clients in 170 countries Location Statement For additional information about location requirements please discuss with the recruiter following submission of your application Being You IBM IBM is committed to creating a diverse environment and is proud to be an equal opportunity employer All qualified applicants will receive consideration for employment without regard to race color religion gender gender identity or expression sexual orientation national origin genetics disability age or veteran status IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status
Full Time
Key Skills :
action, innovation, documentation, ideas, cutting...
Job Description:
Introduction The HR Service Administrator is an integral part of IBM and HR Your goal is to create an outstanding employee experience for IBMers by d...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Scientist I / II - Device Development
associate
Scientist I / II - Device Development
ASTRAZENECA PHARMA INDIA LTD
8-11 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
associate
Scientist I / II - Device Development
12-12-2019
2020-03-11
This position is part of the Device Functionality Safety and Digital Connectivity DFSC team within AstraZenecas Biopharmaceutical Developments Dosage Form Design and Development Groups Device Development Group This position will have responsibility for overseeing planning and or execution of all or various aspects of characterization feasibility test method development and validation design verification testing biocompatibility complaint investigation for primary container and or combination products which may include vials prefilled syringes accessorized prefilled syringes pens cartridges auto-injectors on body injectors and or other drug delivery devices Additional responsibilities may include subject matter expert technical support for operations as part of method transfer and harmonization as well as equipment maintenance calibration and or support Primary responsibilities will include 1 Project support Actively participate in cross-functional project team as Device Functionality and Safety DFS representative by supporting activities which include but are not limited to project planning input requirement generation and risk documentation The DFS representative would take a lead role in coordinating and or executing activities which include characterization and feasibility activities test method development test method validation design verification executed and associated documentation such as plans protocols reports and methods as appropriate 2 Laboratory DFSC team members shall complete activities in a timely manner to ensure access to the laboratory and work in the laboratory in a safe manner DFSC team members are to have familiarity with equipment such as force testing equipment e g Instron non-contact inspection system e g Mitytoyo VQX302 Lansmont transportation system Lansmont drop test equipment calipers rulers and other engineering and scientific tools and equipment 3 Regulations Standards Training DFSC team members may author review and or support documentation data or other materials submitted to regulatory agencies As such DFSC team members are to ensure appropriate GxP working practices are followed for items which may be submitted to regulatory agencies DFSC team members are to be familiar with regulations e g 21 CFR 820 EU MDR as well as standards e g ISO 11040 ISO 11608 DFSC team members are to maintain applicable training and to ensure activities are performed in accordance with current and effective SOPs Education Requirements Educational requirements include a degree in mechanical biomedical chemical or pharmaceutical engineering or a related science technology or engineering field Associate Scientist I BS with 5 years of experience or MS with 2 years of experience Associate Scientist II BS with 8 years of experience or MS with 5 years of experience Job Requirements The candidate should have capability skill and or knowledge in one or more of the following areas Biopharmaceutical combination drug product development Combination product and cGMP regulations and standards Practical laboratory working knowledge Knowledge of laboratory equipment e g Instron QVX302 etc Design verification experimental design statistics data analysis Leadership and interpersonal communication Technical writing and documentation Cross functional collaboration Suitable experience may include development of combination products medical devices and or associated testing activities A high degree of self-motivation engineering skill and technical rigor is required AstraZeneca embraces diversity and equality of opportunity We are committed to building an inclusive and diverse team representing all backgrounds with as wide a range of perspectives as possible and harnessing industry-leading skills We believe that the more inclusive we are the better our work will be We welcome and consider applications to join our team from all qualified candidates regardless of their characteristics We comply with all applicable laws and regulations on non-discrimination in employment and recruitment as well as work authorisation and employment eligibility verification requirements Save for Later
Full Time
Key Skills :
iso, equipment maintenance, safety, product development, calibration...
Job Description:
This position is part of the Device Functionality Safety and Digital Connectivity DFSC team within AstraZenecas Biopharmaceutical Developments Dos...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical Trial Operations
Clinical Trial Operations
PAREXEL International Ltd
2-5 Yrs
14 hrs ago
Canada
Canada
Not Mentioned
IN
0
Canada
Clinical Trial Operations
12-12-2019
2020-03-11
Parexel provides monitors with world class technology training resources and limited protocol load You will also be rewarded for your hard work through our CRA bonus incentive program and career advancement opportunities Your Key Accountabilities Perform all clinical monitoring site management activities for assigned projects in accordance with Parexels standard operating procedures Act as Parexels direct contact with assigned clinical sites and use judgment to assess and ensure overall integrity of study implementation as well as adherence to study protocol Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites Good knowledge of applicable clinical research regulatory requirements i e Good Clinical Practice GCP and International Conference on Harmonization ICH guidelines Function as a mentor and role model for other CRA team members Manage clinical monitoring activities including Arranging on-site visits and logistics Establishment of a site recruitment plan in collaboration with site staff during QV Monitoring completeness and quality of Regulatory Documentation Performing site documentation verification Data collection and drug accountability in accordance with ICH GCP guideline Monitoring patient safety on-site and addressing any violations in a timely manner Qualifications Your Skillset Minimum 2 years of monitoring experience in clinical research Educated to degree level biological science pharmacy or other health related discipline Strong working knowledge of EDC systems and IVRS Experience of CTMS preferred Competent in written and oral English and local language Bilingual in English and French Our Offer We offer you a fascinating and diversified insight into Parexel and an exciting journey through the world of clinical research You can expect to work with a successful highly-qualified and dynamic team as you develop your individual scientific profile You can also look forward to a flexible working environment and a pleasant atmosphere If you are ready to join PAREXELs Journey please apply
Full Time
Key Skills :
regulatory requirements, ich, cra, gcp, regulatory documentation...
Job Description:
Parexel provides monitors with world class technology training resources and limited protocol load You will also be rewarded for your hard work thr...
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INR
Array
Array
Array-Array
"YEARLY"
associate
Engineer , Manufacturing-1
associate
Engineer , Manufacturing-1
STRYKER INDIA
1-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
associate
Engineer , Manufacturing-1
12-12-2019
2020-03-11
This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision This position requires professional mastery of a specialized field of expertise that typically requires a college degree or equivalent Job requires a good knowledge and comprehensive understanding of the range of processes procedures and systems to be used in carrying out assigned tasks and a basic understanding of the underlying concepts principles upon which the job is based The job requires the ability to make judgements based on practice and previous experience This job typically requires a degree in process or equivalent and no experience Your key responsibilities Provide assistance in the procurement contract negotiation installation and validation of new manufacturing equipment tooling and fixtures Liaison with supply chain personnel for the specification and improvement of existing raw materials and process consumables or the sourcing auditing and validation of new suppliers In compliance with QSR requirements provide assistance in the preparation and maintenance of product routings standard operating procedures fixture tooling drawings and Engineering Bill of Materials BOM Will assist subcontractors in resolving manufacturing and quality issues in relation to Audits findings Problem solving and resolution on relevant issues Process validation Technical specifications As part of a cross functional team will assist production in resolving manufacturing and quality issues in relation to Audit findings Problem solving and resolution on relevant issues Scrap and rework analysis and problem solving Development and implementation of structured training programs Will assist in the development and maintenance of products and processes with regard to the following Manufacturing Assembly Procedures Equipment procurement and validation Fixture documentation and validation Process documentation and validation Routing creation and maintenance Problem solving and issue resolution Compliance with standard operating procedures Will execute Engineering Change Orders ECO and Test Reports as necessary Will assist R D department in new product and process development Will provide customer service and team development with regard to Achieving team goals and supporting metrics Setting and achieving training goals and plans Will assist in process improvement production support and troubleshooting on a wide range of CNC controlled and manually operated production equipment What are we looking for Excellent analytical skills Excellent interpersonal communications skills Demonstrated ability to operate small hand tool inspection equipment Demonstrated mechanical and or electrical problem-solving skills Appropriate level work experience obtained through degree program Bachelor Engineering or Bachelor Technology Degree Production Manufacturing Engineering Good computer skills word processing spreadsheets data base Working Knowledge of one of the following programming languages Fortran Visual Basic Visual C Working knowledge of CAD CAM CAE computer systems Working knowledge of CNC Machine Tools and NC programming Strong mathematical knowledge Work From Home No Travel Percentage None
Full Time
Key Skills :
associate
engineer, fixtures, manufacturing, cad/cam, documentation...
Job Description:
This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently wit...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical Trial Operations
Clinical Trial Operations
PAREXEL International Ltd
0-3 Yrs
14 hrs ago
Brazil
Brazil
Not Mentioned
IN
0
Brazil
Clinical Trial Operations
12-12-2019
2020-03-11
Clinical Site Manager CSM serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typical clinical monitor CSMs are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success This includes addressing and resolving site issues and questions You will also manage site quality and delivery from site identification through to close-out As a CSM Parexel will offer you world class technology and training catered to your individual experience You can anticipate less travel and a lower protocol load in comparison to industry peers Your hard work will be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research If impact flexibility and career development appeal to you please apply to learn more Your Key Accountabilities Act as Parexels sole contact with assigned clinical sites Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites generate visit contact report Review the performance of the trial at designated sites ensuring the rights and well-being of human subjects are protected and are in accordance with protocol Evaluate the quality and integrity of the reported data site efficacy and drug accountability Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures SOPs protocol amendment s GCP and the applicable regulatory requirement s Monitor completeness and quality of Regulatory Documentation and perform site document verification Qualifications Your Skillset Site Management experience or equivalent experience in clinical research with understanding of clinical trials methodology and terminology Educated to degree level biological science pharmacy or other health related discipline Demonstrates strong interpersonal written and verbal communication skills within a matrixed team Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight Client focused approach to work flexible attitude with respect to work assignments and new learning Ability to manage multiple tasks to evaluate a variety of unpredictable scenarios and achieve project timelines apply understanding of study protocol s Work ethically and honestly to promote the development of life changing treatments for patients Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System CTMS Electronic Document Management System EDMS and MS-Office products such as Excel and Word Our Offer Join the best minds in the industry and leverage your expertise to help advance treatments into the hands of those who need them most This role is an excellent opportunity to enhance your skills and take the lead on client projects We look forward to speaking with you and determining how Parexel fits into your career journey
Full Time
Key Skills :
regulatory, gcp, clinical trials, regulatory documentation, clinical...
Job Description:
Clinical Site Manager CSM serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typi...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Spot Buy
associate
Spot Buy
associate
Allstate solutions private limited
4-6 Yrs
14 hrs ago
Hyderabad
Hyderabad
Telangana State
IN
0
Hyderabad
Spot Buy
associate
12-12-2019
2020-03-11
Company Allstate Company Sr Consultant with 4-6 years of hands-on development experience in native iOS mobile app development using Phonegap Additional knowledge of iOS frameworks Idea about RESTful web services Should have good communication skills Sr COnsultant develops code for intermediate to complex modules participates in design reviews conducts code reviews creates test plans and participates in testing reviews and resolves moderate to complex defects This position designs documents reviews and maintains components of solutions for intermediate projects This application developer will join a team of technical professionals that work on Mobile Applications for the Allstate Consumer Job Responsibilities The Sr Consultant Application Developer develops code for intermediate modules participates in design reviews conducts code reviews creates test plans and participates in testing reviews and resolves moderate defects The Sr Consultant Application Developer designs documents reviews and maintains components of solutions for intermediate projects It also includes reacting to production problems or supporting production changes where those applications are operating Evaluate detailed business functional and high-level technical requirements including recovery security and audit Design detailed technical components with high-level architecture Recognize and understand use of design patterns for intermediate applications Apply reusability and future state architectures Participates and provides feedback in design reviews Complete component design documents on assigned projects Participate and provide feedback in design reviews Develop or confirm detailed project or system change estimates or project plans Calibrates estimating factors for continuous process improvement Develop code for intermediate modules following documentation and development standards Create enhanced technical documentation and implement changes Acts a technical expert for consultant application developer s Conduct timely structured code reviews to ensure standards and systems interoperability Review and critique team members code
Full Time
Key Skills :
technical expert, production, action, documentation, process improvement...
Job Description:
Company Allstate Company Sr Consultant with 4-6 years of hands-on development experience in native iOS mobile app development using Phonegap Ad...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Senior Director , Clinical Development , Oncology
Senior Director , Clinical Development , Oncology
ASTRAZENECA PHARMA INDIA LTD
5-8 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Senior Director , Clinical Development , Oncology
12-12-2019
2020-03-11
With one of the largest most robust pipelines in the industry including more than 120 research projects and product candidates We are focused on three core therapeutic areas Oncology Respiratory Inflammation and Autoimmune and Cardiovascular and Metabolic Disease Oncology is one of the 5 key growth platforms for the companys future success and we have an ambitious vision of delivering 6 new medicines to patients by 2020 Our strategy underpinning this vision is to target areas of unmet need incorporate biomarker-driven patient selection maximize value across tumor types and stages of disease and focus on development of novel combinations Were constantly pushing the boundaries of science to deliver life-changing medicines to patients with a passion for discovery and a pipeline to show for it Were pioneering innovative research and exploring novel pathways across key therapeutic areas including oncology respiratory inflammation and autoimmunity cardiovascular and metabolic disease and infection and vaccines And were industry-leading in immunology protein engineering and translational science We offer a unique and strong collaborative network as part of the AstraZeneca family as together we explore synergies between small and large molecules Position Summary We are seeking a well-trained clinician with strong leadership skills who is driven by science and the desire to develop novel Oncology drug therapies for cancer patients and who has a mastery of the drug development process especially early phase clinical trials protocol writing study conduct data review and reconciliation the principles of translational medicine and what it takes to lead teams successfully Director Senior Director Clinical Development Oncology will be based in Waltham MA Gaithersburg MD and Wilmington DE and will report to the Vice President Clinical Development Other responsibilities include Leading a team of Clinical Development professionals responsible for delivering against Oncology Drug Development projects Full responsibility for the planning implementation and daily operation of a drug development projects Collaborate with key internal and external stakeholders Contribute to and support Department Clinical initiatives to improve the quality and content of all clinical programs as well as the cross functional organization processes designed to effectively deliver our R D portfolio Specific duties and major responsibilities include Direct Oversee the design and implementation of early stage clinical projects as a member of our
Full Time
Key Skills :
data management, regulatory, regulatory documents,
research
, clinical trials...
Job Description:
With one of the largest most robust pipelines in the industry including more than 120 research projects and product candidates We are focused on th...
Apply Now
INR
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Array
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"YEARLY"
Director , Clinical Development
Director , Clinical Development
ASTRAZENECA PHARMA INDIA LTD
2-5 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Director , Clinical Development
12-12-2019
2020-03-11
Other locations Gaithersburg MD and Wilmington DE With one of the largest most robust pipelines in the industry including more than 120 research projects and product candidates We are focused on three core therapeutic areas Oncology Respiratory Inflammation and Autoimmune and Cardiovascular and Metabolic Disease Oncology is one of the 5 key growth platforms for the companys future success and we have an ambitious vision of delivering 6 new medicines to patients by 2020 Our strategy underpinning this vision is to target areas of unmet need incorporate biomarker-driven patient selection maximize value across tumor types and stages of disease and focus on development of novel combinations Were constantly pushing the boundaries of science to deliver life-changing medicines to patients with a passion for discovery and a pipeline to show for it Were pioneering innovative research and exploring novel pathways across key therapeutic areas including oncology respiratory inflammation and autoimmunity cardiovascular and metabolic disease and infection and vaccines And were industry-leading in immunology protein engineering and translational science We offer a unique and strong collaborative network as part of the AstraZeneca family as together we explore synergies between small and large molecules Position Summary We are seeking a well-trained clinician with strong leadership skills who is driven by science and the desire to develop novel Oncology therapies for cancer patients and who has a mastery of the drug development process especially early phase clinical trials protocol writing study conduct data review and reconciliation the principles of translational medicine and what it takes to lead teams successfully Director Senior Director Clinical Development Oncology will be based in Waltham MA Gaithersburg MD or Wilmington DE and will report to the Vice President Clinical Development Oncology Other responsibilities include Leading a team of Clinical Development professionals responsible for delivering against Oncology Drug Development projects Full responsibility for the planning implementation and daily operation of a drug development projects Collaborate with key internal and external stakeholders Contribute to and support Department Clinical initiatives to improve the quality and content of all clinical programs as well as the cross functional organization processes designed to effectively deliver our R D portfolio Specific duties and major responsibilities include Direct Oversee the design and implementation of early stage clinical projects as a member of our Product Development Team PDT and leader of the Clinical Sub-Team CST Ensure that the overall scientific and medical content of all clinical programs is scientifically and clinically rigorous Prepare clinical development plans that integrate pre-clinical and early clinical findings while working to ensure cross-functional alignment on an ongoing basis throughout the early phases of clinical development Design scientifically rigorous and maximally cost-effective clinical protocols that are aligned with the clinical development plan Present and defend protocols and clinical development plans at internal governance forums Serve as Medical Monitor responsible for the safety monitoring of clinical trials and as medical
Full Time
Key Skills :
regulatory documents,
research
, clinical trials, immunology, clinical study...
Job Description:
Other locations Gaithersburg MD and Wilmington DE With one of the largest most robust pipelines in the industry including more than 120 research ...
Apply Now
INR
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Array
Array-Array
"YEARLY"
Study Manager
Study Manager
Pfizer Inc.
5-8 Yrs
14 hrs ago
China
China
Not Mentioned
IN
0
China
Study Manager
12-12-2019
2020-03-11
Protocol Development Provide comprehensive operational input to the protocol design to ensure operational feasibility Responsible for conducting the protocol feasibility prior to finalization of the CPEs as appropriate Generate study level ICD as appropriate Budget Provide input to the generation of investigator grant budgets at the study level identify required budget components Initiate review and ensure approval of the study start-up budget including per subject and ancillary investigator costs and Clinical Trial Budget or MPA Data Management GCDS Interactions Partner with GCDS to ensure set up of data capture tools CRFs EDC system diary cards questionnaires translations etc to ensure completion within project deliverable timelines Overall responsible for ensuring the study has efficient and effective data flows for all types of study data including SAEs endpoints patient diaries lab data etc Subject Recruitment Country Allocation Site Selection Start-up as appropriate Conduct study level allocation including country and study level feasibility assessments to ensure appropriate site selection in China Develop study level recruitment retention strategy plan oversee implementation of plan including site-level plans recruitment retention tools and advertising materials Oversee sites and site management to ensure timely site selection and site readiness Clinical Site Agreements Ethics Committee approvals and regulatory documentation Partner with Project Planner and study team members to develop study level plans and processes to ensure alignment with overall Development Plan Training Investigator Meeting as appropriate Develop the Monitoring Plan ensure sites and CRAs are trained on Protocol-Specific aspects of the Study Monitoring Plan Responsible for working with Clinician to ensure that CRAs are provided with appropriate training of protocol and knowledge of respective therapeutic area Drive and or contributes to investigator meeting strategy agenda and responsible for overseeing implementation by the project team review meeting objectives materials Facilitate and presentation investigator meetings on study progress update and etc as upon request of project team Drug Supply Collaborate with Supply Chain Lead to develop and complete the Request for Clinical Supplies Work with the Supply Chain Lead to ensure that clinical trial drug supplies are ordered produced labeled and supplied in a timely manner Communications and Tracking Deliverables Track progress to ensure all essential study materials equipment and documentation are in place for study start e g ethics and regulatory approval budget drug supplies data collection tools Provide update of study status to study team as appropriate Clinical Study Conduct Subject Recruitment Retention Manage protocol-level subject recruitment and retention and take appropriate action to ensure targets are met Quality Compliance Management Periodically review protocol deviations and collaborate with clinicians to manage protocol deviations according to Pfizer SOP Works closely with study team to ensure data quality requirements are agreed and met prior to reporting Perform required activities to ensure quality and completeness of Trial Master File and any additional regulatory documentation Work with quality assurance line to establish appropriate QC audit and inspection plans Serves as central point of contact for site and sponsor audits Supports the writing of appropriate audit responses and ensures actions are completed Leads and oversees the study risk planning process e g IQMP Oversees operational metrics across study and manages trends and escalations Ensures maintenance and accuracy of Standard Operating Procedures SOP log Leads awareness and resolution of Significant Quality Events SQEs and escalations Monitors and remediates quality metrics and completes remediation tracker Conduct and report oversight activities both remote and onsite visits according to Pfizer standards Data Flow Management Partners with GCDS and site management functional lines to ensure timely retrieval and database entry of CRFs and other clinical study data and the distribution and resolution of data queries Coordinates endpoint collection reconciliation and adjudication when required Coordinates data collection and cleaning for interim data locks e g DSMBs Planned interim analysis Final Safety Updates etc Ensures Quality Gate timing planning and team readiness CRO Vendor Management Effective management of external vendors including SMOs and CROs Budget Compiles components of protocol level budget Approve up front or initial payments to investigators and vendors Drug Supply Work with Supply Chain Lead to ensure drug supply including resupply process timelines risks and issues are handled in a timely manner Communications and Tracking Deliverables Monitor cross-site performance and raise issues to CRAs for awareness Responsible for distribution of protocol level to CRAs and then ensure investigational sites are fully informed in timely manner Manages study team communications to ensure cross-functional connectivity among study team members and supporting functional lines Clinical Study Close-out In close partnership with the CRAs to ensure site closeout activities are completed Responsible for the collection and consolidation of the Protocol Deviation Logs Accountable for study close out support GCDS in database lock and release activities ensuring all timelines and quality goals are met Contributes information regarding study conduct as required to ensure effective and timely study reporting Participates in review of study report as appropriate Responsible for inspection readiness at a study level with site facing activities such as self-inspection remaining the responsibility of the Study Management group Technical Competencies Competency Detail Comments specific skills etc Scientific and drug development expertise Clinical study expertise Problem solving Decision Making Organizational skills Communication skills Project process management Administrative excellence Clinical Scientific aptitude Technology management Budget expense management Understanding of scientific clinical principles and ability to work across different therapeutic areas Knowledge of working with complex and novel emerging technologies and interpret and incorporate them within the context of a clinical trial Extensive knowledge of clinical development process including in depth knowledge and understanding of the principles of GCP Ability to understand and influence Site Investigators Key Opinion Leaders on non-medical related issues Working knowledge of the principles and
Full Time
Key Skills :
site selection, regulatory requirements, gcp, clinical trials, clinical study...
Job Description:
Protocol Development Provide comprehensive operational input to the protocol design to ensure operational feasibility Responsible for conducting the...
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INR
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Array
Array-Array
"YEARLY"
Salesforce Administrator
Salesforce Administrator
Nielsen Research Ltd. Co.
0-3 Yrs
14 hrs ago
United Kingdom, Uk
United Kingdom
,
Not Mentioned
IN
0
United Kingdom
Uk
Not Mentioned
IN
0
Uk
Salesforce Administrator
12-12-2019
2020-03-11
Salesforce Administrator Nielsen Brandbank - Norwich UK ABOUT THIS JOB The Salesforce Administrator will be responsible for the proactive planning implementation and support of our global customer relationship management system CRM and to ensure that Salesforce is being fully utilised to meet key business objectives This individual will act as the Nielsen Brandbank CRM knowledge expert and will execute the day to day support and improvement of the CRM platform embracing the challenge of solving critical business problems RESPONSIBILITIES Salesforce administrator for the Nielsen Brandbank global sales teams Responsible for the implementation adoption and enhancement of the Salesforce platform across the global organisation Daily administration and support of the Salesforce application and sales users including but not limited to managing multiple user setup profiles and roles customization of objects fields record types page layouts and validations Explore innovative and automated approaches identifying those that leverage our resources and provide economies of scale Evaluate new Salesforce releases and apps owning and managing plans for implementation Develop create and maintain customized reports and dashboards Work with business stakeholders to define required features and map salesforce features to business processes Assist with training and the creation of training materials and user documentation for processes policies and application configurations Continuous improvement via self-learning training and certifications to stay abreast of technology advancements A LITTLE BIT ABOUT YOU As the Salesforce Administrator you will work closely with our global sales teams to ensure that we are maximising efficiency and capitalizing on the full features and benefits that the system has to offer We are looking for someone that thrives on working in a fast paced and constantly evolving environment You will be passionate enthusiastic and forward thinking with excellent technical and communication skills who can effectively collaborate with key stakeholders at all levels across the business QUALIFICATIONS Strong understanding of Salesforce best practices and functionality Demonstrable experience as a Salesforce Administrator Salesforce Administrator certified or equivalent experience and willingness to work towards certification Demonstrable ability to meet deadlines effectively prioritise and execute multiple requests at any one time in a fast paced and ever changing environment Experience of proactively driving change projects through to successful completion Ability to understand and articulate complex business requirements and translate into solutions Demonstrated technical competence underpinned by commercial application Creative and analytical thinker with strong attention to detail and problem solving skills Excellent written and verbal communication skills with an ability to build and sustain effective relationships Experience of working with Sales Teams would be advantageous
Full Time
Key Skills :
problem solving, salesforce, user documentation, crm...
Job Description:
Salesforce Administrator Nielsen Brandbank - Norwich UK ABOUT THIS JOB The Salesforce Administrator will be responsible for the proactive planning...
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INR
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Array
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"YEARLY"
Initiation Clinical Site Manager I
Initiation Clinical Site Manager I
PAREXEL International Ltd
0-3 Yrs
14 hrs ago
United Kingdom, Uk
United Kingdom
,
Not Mentioned
IN
0
United Kingdom
Uk
Not Mentioned
IN
0
Uk
Initiation Clinical Site Manager I
12-12-2019
2020-03-11
Parexel is in the business of improving the worlds health We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments From clinical trials to regulatory consulting and market access our therapeutic technical and functional ability is underpinned by a deep conviction in what we do We believe in our values Patients First Quality Respect Empowerment Accountability We are currently hiring an experienced Study Start up Specialist for our Uxbridge office Candidates must have strong previous study start up experience working in the CRO industry Please apply below if you are interested and have the relevant SSU experience This role will be based at our UK Head Office situated in Uxbridge This is close to both Uxbridge train station as well as the town centre and the building has plenty of free parking The Initiation Clinical Site Manager II will specialise in Pre SIV activities will be assigned and accountable for managing and driving the strategy for the Pre SIV start up tasks of the study The iCSM II can also support protocol amendments if applicable Your Key Accountabilities Start-Up from site identification through pre-initiation - Act as Parexels direct point of contact with assigned sites accountable for quality and delivery during the start-up phase - Build relationships with investigators and site staff - Conduct drive and manage country specific feasibility and or site pre-qualification and qualification activities which may include - Preparation negotiation and facilitation of execution of Confidentiality Agreements CDA Clinical Site Agreements CSAs and any amendments - Conduct remote Qualification Visits QVs - Generate visit contact reports using judgment to identify site issues and problem solving to direct resolution - Develop strategy to configure distribute and collect and review and approve high quality country specific and or site specific documents or essential regulatory documents SRP and any updated or amended regulatory documentation - Customize review and negotiate as needed country site specific Informed Consent Forms ICF translations within parameters of country regulatory client requirements and customize and negotiate any amendments - Prepare and submit IRB IEC application s resolving conflicts determining appropriate follow up until receipt of final approval - Submit all pertinent documentation to the trial master file as per project plans sponsor company policy - Forecast develop manage and revise plans and strategies for - IRB IEC submission approval - Site activation - Patient recruitment retention - Update and maintain appropriate Clinical Trial Management systems CTMS in a timely manner - Promptly identify use judgment and knowledge to address and resolve or escalate any site question and or issue including but not limited to potential issues or risks with site activation timelines issues with patient recruitment strategy deficiencies in training data quality or integrity study non-compliance etc - Facilitate and support allocated sites with access to relevant study systems and ensure they are compliant with all project specific training requirements prior to study start - Actively participate in Investigator and other external or internal meetings audits regulatory inspections - Work in a self-driven capacity with limited need for oversight - Proactively keep manager informed about work progress and any issues Qualifications Education - Educated to degree level biological science pharmacy or other health-related discipline preferred or equivalent nursing qualification or other equivalent experience Skills - Strong problem solving skills - Able to take initiative and work independently and to proactively seek guidance when necessary - Excellent presentation skills - Client focused approach to work - Ability to interact professionally within a client organization - Flexible attitude with respect to work assignments and new learning - Ability to prioritize multiple tasks and achieve project timelines utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise - Strong ability to make appropriate decisions in ambiguous situations - Willingness to work in a matrix environment and to value the importance of teamwork - Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System CTMS Electronic Document Management System EDMS and MS-Office products such as Excel and Word - Excellent interpersonal verbal and written communication skills - Sense of urgency in completing assigned tasks and ability to assist others to meet study country deliverables - Excellent time management in order to meet study needs team objectives and department goals - Proven ability to work across cultures - Shows commitment to and performs consistently high quality work - Ability to successfully work in a virtual team environment - Consulting Skills - Able to accommodate travel time requirements according to tasks allocation phase of the study assigned - Act as a mentor and role model for other team members - Effectively enlist the support of team members in meeting goals - Attention to detail Knowledge and Experience - Intermediate level study set up site initiation study start up experience or equivalent experience in clinical research environment with understanding of clinical trials methodology and terminology - Strong previous Clinical Site Agreement CSA and site contracts experience is desirable for both new and exisitng study amendments In return we will be able to offer you a structured career pathway and development within the role including awareness and understanding of the industry Your hard work will be rewarded with a competitive base salary as well as a benefits package including 25 days holiday per year strong contributory pension scheme life assurance long term disability private medical and private dental cover as well as other leading edge benefits that you would expect with a company of this type If you are ready to join Parexels Journey please apply
Full Time
Key Skills :
regulatory documents, clinical trials, regulatory documentation, clinical, clinical
research
...
Job Description:
Parexel is in the business of improving the worlds health We do this by providing a suite of biopharmaceutical services that help clients across the ...
Apply Now
INR
Array
Array
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"YEARLY"
Quality
associate
I , Receiving & Inspection
Quality
associate
I , Receiving & Inspection
Baxter India Pvt Ltd
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Quality
associate
I , Receiving & Inspection
12-12-2019
2020-03-11
Quality Associate I Receiving Inspection Req JR - 007384 Location Round Lake IL US Job Category Quality Baxter International Around the world our employees are united by our mission to save and sustain lives Together we create a culture that encourages colleagues to pursue rewarding careers where everyone has the opportunity to do meaningful work as a part of a team they respect in an environment that values each persons contributions Were happy youre interested in continuing your career journey with Baxter Summary Quality Associate performs daily quality review of raw material documentation to ensure that materials being received are produced in accordance to Company methodology procedures and standards Quality Associate completes Change Control Supplier Quality and Nonconformance and Corrective Action Preventive Action CAPA quality records related to Receiving Inspection Quality Associate is SME for Receiving Inspection procedures and manages projects The candidate must not be allergic to Penicillin or Cephalosporin drugs Essential Responsibilities Reviews and approves documentation for API Active Pharmaceutical Ingredients Excipients Chemicals Laminated Rollstock Printed Direction Inserts Labels and Cartons Provides Receiving and Inspection review support for materials purchased by Takeda Manages raw material tracking log and scheduling work for R I technicians Manages RLDD Stability schedule and sends out Stability notices Strong computer literacy preferred experience with material inventory management systems Creates reassay and expiration report on a monthly basis Completes GME and Labvantage setups for materials Supplier Quality SQ responsibilities to include SCAR Supplier Corrective Action Request writing and review Reduced testing of materials - new and periodic review SQ approval of raw material part records and Risk Action and Mitigation RAM review for Round Lake Drug Delivery Owns and manages Change Control records Performs investigations for R I nonconformances and owns R I related CAPAs Performs R I procedure and training code revisions in document system Completes Certification of Documentation Review CDR process for raw materials to implement them in the plant systems Validation and testing of computerized systems to include writing and executing a protocol Submit and manage purchase orders in Coupa system Manages quotes and sends samples to external testing labs Complete and manage R I Preventive Maintenance PM records in the Maximo system Attends various Tier and Cross-Functional meetings as the R I representative Secondary responsibilities to support production as needed Releases materials for production after quality inspections and or tests are completed and acceptable Performs proofreading and laminated rollstock thickness testing Monitors and verifies quality in accordance with statistical processes and other control procedures Uses small hand tools and various measuring and testing devices in performing quality tests Will work in both Drug Delivery and Penicillin facilities as needed Job Requirements The candidate must not be allergic to Penicillin or Cephalosporin drugs Minimum Associates Degree and one to three years of relevant experience required OR Bachelors degree and experience with a medical device pharma or other similarly regulated industry preferred Good writing and verbal communication skills and problem-solving skills are required Ability to work in a team environment and make independent decisions based on procedural and regulatory requirements Complete understanding of cGMPs and GDP procedures 20 30 vision in at least one eye with or without corrective lenses The candidate must be able to work flexible hours in a dynamic environment with minimal direct supervision Equal Employment Opportunity Baxter is an equal opportunity employer Baxter evaluates qualified applicants without regard to race color religion gender national origin age sexual orientation gender identity or expression protected veteran status disability handicap status or any other legally protected characteristic EEO is the Law EEO is the law - Poster Supplement Pay Transparency Policy Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities If because of a medical condition or disability you need a reasonable accommodation for any part of the application or interview process please send an e-mail to Americas TTA baxter com and let us know the nature of your request along with your contact information
Full Time
Key Skills :
production, preventive maintenance, corrective action, supervision, scheduling...
Job Description:
Quality Associate I Receiving Inspection Req JR - 007384 Location Round Lake IL US Job Category Quality Baxter International Around the w...
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INR
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Array
Array-Array
"YEARLY"
Clinical Trial Operations
Clinical Trial Operations
PAREXEL International Ltd
0-3 Yrs
14 hrs ago
United Kingdom, Uk
United Kingdom
,
Not Mentioned
IN
0
United Kingdom
Uk
Not Mentioned
IN
0
Uk
Clinical Trial Operations
12-12-2019
2020-03-11
Parexel has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction Within this model the Clinical Site Manager CSM formerly the Clinical Research Associate CRA serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typical clinical monitor CSMs are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success This includes addressing and resolving site issues and questions You will also manage site quality and delivery from site identification through to close-out As a CSM Parexel will offer you world class technology and training catered to your individual experience You can anticipate less travel and a lower protocol load in comparison to industry peers Your hard work will be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research If impact flexibility and career development appeal to you please apply to learn more Your Key Accountabilities Act as Parexels sole contact with assigned clinical sites Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites generate visit contact report Review the performance of the trial at designated sites ensuring the rights and well-being of human subjects are protected and are in accordance with protocol Evaluate the quality and integrity of the reported data site efficacy and drug accountability Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures SOPs protocol amendment s GCP and the applicable regulatory requirement s Monitor completeness and quality of Regulatory Documentation and perform site document verification Qualifications Your Skillset Substantial Site Management experience or equivalent experience in clinical research with understanding of clinical trials methodology and terminology Educated to degree level biological science pharmacy or other health related discipline Demonstrates strong interpersonal written and verbal communication skills within a matrixed team Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight Client focused approach to work flexible attitude with respect to work assignments and new learning Ability to manage multiple tasks to evaluate a variety of unpredictable scenarios and achieve project timelines apply understanding of study protocol s Work ethically and honestly to promote the development of life changing treatments for patients Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System CTMS Electronic Document Management System EDMS and MS-Office products such as Excel and Word Our Offer Join the best minds in the industry and leverage your expertise to help advance treatments into the hands of those who need them most This role is an excellent opportunity to enhance your skills and take the lead on client projects We look forward to speaking with you and determining how Parexel fits into your career journey EEO DisclaimerPAREXEL is an equal opportunity employer Qualified applicants will receive consideration for employment without regard to legally protected status which in the US includes race color religion sex sexual orientation gender identity national origin disability or protected veteran status
Full Time
Key Skills :
regulatory, cra, gcp, clinical trials, regulatory documentation...
Job Description:
Parexel has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction With...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical Trial Operations
Clinical Trial Operations
PAREXEL International Ltd
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Clinical Trial Operations
12-12-2019
2020-03-11
Clinical Site Manager CSM serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typical clinical monitor CSMs are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success This includes addressing and resolving site issues and questions You will also manage site quality and delivery from site identification through to close-out As a CSM Parexel will offer you world class technology and training catered to your individual experience You can anticipate less travel and a lower protocol load in comparison to industry peers Your hard work will be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research If impact flexibility and career development appeal to you please apply to learn more Your Key Accountabilities Act as Parexels sole contact with assigned clinical sites Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites generate visit contact report Review the performance of the trial at designated sites ensuring the rights and well-being of human subjects are protected and are in accordance with protocol Evaluate the quality and integrity of the reported data site efficacy and drug accountability Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures SOPs protocol amendment s GCP and the applicable regulatory requirement s Monitor completeness and quality of Regulatory Documentation and perform site document verification Qualifications Your Skillset Site Management experience or equivalent experience in clinical research with understanding of clinical trials methodology and terminology Educated to degree level biological science pharmacy or other health related discipline Demonstrates strong interpersonal written and verbal communication skills within a matrixed team Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight Client focused approach to work flexible attitude with respect to work assignments and new learning Ability to manage multiple tasks to evaluate a variety of unpredictable scenarios and achieve project timelines apply understanding of study protocol s Work ethically and honestly to promote the development of life changing treatments for patients Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System CTMS Electronic Document Management System EDMS and MS-Office products such as Excel and Word Our Offer Join the best minds in the industry and leverage your expertise to help advance treatments into the hands of those who need them most This role is an excellent opportunity to enhance your skills and take the lead on client projects We look forward to speaking with you and determining how Parexel fits into your career journey
Full Time
Key Skills :
regulatory, gcp, clinical trials, regulatory documentation, clinical...
Job Description:
Clinical Site Manager CSM serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typi...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical Trial Operations
Clinical Trial Operations
PAREXEL International Ltd
0-3 Yrs
14 hrs ago
Spain
Spain
Not Mentioned
IN
0
Spain
Clinical Trial Operations
12-12-2019
2020-03-11
PAREXEL has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction Within this model the Clinical Site Manager CSM formerly the Clinical Research Associate CRA serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typical clinical monitor CSMs are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success This includes addressing and resolving site issues and questions You will also manage site quality and delivery from site identification through to close-out As a CSM PAREXEL will offer you world class technology and training catered to your individual experience You can anticipate less travel and a lower protocol load in comparison to industry peers Your hard work will be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research If impact flexibility and career development appeal to you please apply to learn more Your Key Accountabilities Act as PAREXELs sole contact with assigned clinical sites Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites generate visit contact report Review the performance of the trial at designated sites ensuring the rights and well-being of human subjects are protected and are in accordance with protocol Evaluate the quality and integrity of the reported data site efficacy and drug accountability Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures SOPs protocol amendment s GCP and the applicable regulatory requirement s Monitor completeness and quality of Regulatory Documentation and perform site document verification Qualifications Your Skillset Site Management experience or equivalent experience in clinical research with understanding of clinical trials methodology and terminology Educated to degree level biological science pharmacy or other health related discipline Demonstrates strong interpersonal written and verbal communication skills within a matrixed team Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight Client focused approach to work flexible attitude with respect to work assignments and new learning Ability to manage multiple tasks to evaluate a variety of unpredictable scenarios and achieve project timelines apply understanding of study protocol s Work ethically and honestly to promote the development of life changing treatments for patients Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System CTMS Electronic Document Management System EDMS and MS-Office products such as Excel and Word Our Offer Join the best minds in the industry and leverage your expertise to help advance treatments into the hands of those who need them most This role is an excellent opportunity to enhance your skills and take the lead on client projects We look forward to speaking with you and determining how PAREXEL fits into your career journey
Full Time
Key Skills :
regulatory, cra, gcp, clinical trials, regulatory documentation...
Job Description:
PAREXEL has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction With...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical Trial Operations
Clinical Trial Operations
PAREXEL International Ltd
0-3 Yrs
14 hrs ago
France
France
Not Mentioned
IN
0
France
Clinical Trial Operations
12-12-2019
2020-03-11
PAREXEL has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction Within this model the Clinical Site Manager CSM formerly the Clinical Research Associate CRA serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typical clinical monitor CSMs are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success This includes addressing and resolving site issues and questions You will also manage site quality and delivery from site identification through to close-out As a CSM PAREXEL will offer you world class technology and training catered to your individual experience You can anticipate less travel and a lower protocol load in comparison to industry peers Your hard work will be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research If impact flexibility and career development appeal to you please apply to learn more Your Key Accountabilities Act as PAREXELs sole contact with assigned clinical sites Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites generate visit contact report Review the performance of the trial at designated sites ensuring the rights and well-being of human subjects are protected and are in accordance with protocol Evaluate the quality and integrity of the reported data site efficacy and drug accountability Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures SOPs protocol amendment s GCP and the applicable regulatory requirement s Monitor completeness and quality of Regulatory Documentation and perform site document verification Qualifications Your Skillset Previous relevant work experience preferred Educated to degree level biological science pharmacy or other health related discipline Demonstrates strong interpersonal written and verbal communication skills within a matrixed team Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight Client focused approach to work flexible attitude with respect to work assignments and new learning Ability to manage multiple tasks to evaluate a variety of unpredictable scenarios and achieve project timelines apply understanding of study protocol s Work ethically and honestly to promote the development of life changing treatments for patients Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System CTMS Electronic Document Management System EDMS and MS-Office products such as Excel and Word Our Offer Join the best minds in the industry and leverage your expertise to help advance treatments into the hands of those who need them most This role is an excellent opportunity to enhance your skills and take the lead on client projects We look forward to speaking with you and determining how PAREXEL fits into your career journey
Full Time
Key Skills :
regulatory, cra, gcp, regulatory documentation, clinical
research
associate
...
Job Description:
PAREXEL has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction With...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clerk ,
associate
Store
Clerk ,
associate
Store
WALMART INDIA
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Clerk ,
associate
Store
12-12-2019
2020-03-11
What youll do at Provides customer service by acknowledging the customer identifying customer needs assisting with purchasing decisions locating merchandise resolving customer issues and concerns retrieving and organizing carts flatbed assisting customers with transporting items loading merchandise into customer vehicles and promoting products and services while maintaining store environment according to associate store policies and procedures Maintains merchandise presentation by stocking merchandise removing damaged or out-of-date goods setting up cleaning and organizing product displays signing researching for example internet Walmart systems merchandise prices to price items appropriately and securing fragile and high theft merchandise Maintains area of responsibility in accordance with associate store policies and procedures by zoning the area of responsibility arranging and organizing merchandise supplies identifying shrink and damages Cleans all areas of the associate store both inside and outside by utilizing tools machines and company-approved chemicals and performing routine maintenance on machines and other equipment in accordance with company policies and procedures Receives merchandise and organizes and maintains the backroom by following company safety cleaning and operating policies and procedures receiving sorting staging and delivering merchandise and completing paperwork logs and other required documentation Processes customer transactions by operating equipment for example cash registers and related tools ensuring compliance with company policies and procedures for different payment types and items sold Minimum Qualifications Outlined below are the required minimum qualifications for this position If none are listed there are no minimum qualifications Preferred Qualifications Outlined below are the optional preferred qualifications for this position If none are listed there are no preferred qualifications Customer Service Facilities Planning About Walmart At Walmart we help people save money so they can live better This mission serves as the foundation for every decision we make from responsible sourcing to sustainabilityand everything in between As a Walmart associate you will play an integral role in shaping the future of retail tech merchandising finance and hundreds of other industriesall while affecting the lives of millions of customers all over the world Here your work makes an impact every day What are you waiting for
Full Time
Key Skills :
documentation, vehicles, planning, safety, maintenance...
Job Description:
What youll do at Provides customer service by acknowledging the customer identifying customer needs assisting with purchasing decisions locating me...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical Trial Operations
Clinical Trial Operations
PAREXEL International Ltd
1-3 Yrs
14 hrs ago
Belgium
Belgium
Not Mentioned
IN
0
Belgium
Clinical Trial Operations
12-12-2019
2020-03-11
PAREXEL has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction Within this model the Clinical Site Manager CSM formerly the Clinical Research Associate CRA serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typical clinical monitor CSMs are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success This includes addressing and resolving site issues and questions You will also manage site quality and delivery from site identification through to close-out As a CSM PAREXEL will offer you world class technology and training catered to your individual experience You can anticipate less travel and a lower protocol load in comparison to industry peers Your hard work will be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research If impact flexibility and career development appeal to you please apply to learn more Your Key Accountabilities Act as PAREXELs sole contact with assigned clinical sites Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites generate visit contact report Review the performance of the trial at designated sites ensuring the rights and well-being of human subjects are protected and are in accordance with protocol Evaluate the quality and integrity of the reported data site efficacy and drug accountability Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures SOPs protocol amendment s GCP and the applicable regulatory requirement s Monitor completeness and quality of Regulatory Documentation and perform site document verification Qualifications Your Skillset Substantial Site Management experience or equivalent experience in clinical research with understanding of clinical trials methodology and terminology Educated to degree level biological science pharmacy or other health related discipline Demonstrates strong interpersonal written and verbal communication skills within a matrixed team Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight Client focused approach to work flexible attitude with respect to work assignments and new learning Ability to manage multiple tasks to evaluate a variety of unpredictable scenarios and achieve project timelines apply understanding of study protocol s Work ethically and honestly to promote the development of life changing treatments for patients Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System CTMS Electronic Document Management System EDMS and MS-Office products such as Excel and Word Our Offer Join the best minds in the industry and leverage your expertise to help advance treatments into the hands of those who need them most This role is an excellent opportunity to enhance your skills and take the lead on client projects
Full Time
Key Skills :
regulatory, cra, gcp, clinical trials, regulatory documentation...
Job Description:
PAREXEL has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction With...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical Trial Operations
Clinical Trial Operations
PAREXEL International Ltd
0-3 Yrs
14 hrs ago
Poland
Poland
Not Mentioned
IN
0
Poland
Clinical Trial Operations
12-12-2019
2020-03-11
PAREXEL has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction Within this model the Clinical Site Manager CSM formerly the Clinical Research Associate CRA serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typical clinical monitor CSMs are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success This includes addressing and resolving site issues and questions You will also manage site quality and delivery from site identification through to close-out As a CSM PAREXEL will offer you world class technology and training catered to your individual experience You can anticipate less travel and a lower protocol load in comparison to industry peers Your hard work will be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research If impact flexibility and career development appeal to you please apply to learn more Your Key Accountabilities Act as PAREXELs sole contact with assigned clinical sites Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites generate visit contact report Review the performance of the trial at designated sites ensuring the rights and well-being of human subjects are protected and are in accordance with protocol Evaluate the quality and integrity of the reported data site efficacy and drug accountability Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures SOPs protocol amendment s GCP and the applicable regulatory requirement s Monitor completeness and quality of Regulatory Documentation and perform site document verification Qualifications Your Skillset Substantial Site Management experience or equivalent experience in clinical research with understanding of clinical trials methodology and terminology Educated to degree level biological science pharmacy or other health related discipline Demonstrates strong interpersonal written and verbal communication skills within a matrixed team Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight Client focused approach to work flexible attitude with respect to work assignments and new learning Ability to manage multiple tasks to evaluate a variety of unpredictable scenarios and achieve project timelines apply understanding of study protocol s Work ethically and honestly to promote the development of life changing treatments for patients Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System CTMS Electronic Document Management System EDMS and MS-Office products such as Excel and Word Our Offer Join the best minds in the industry and leverage your expertise to help advance treatments into the hands of those who need them most This role is an excellent opportunity to enhance your skills and take the lead on client projects
Full Time
Key Skills :
regulatory, cra, gcp, clinical trials, regulatory documentation...
Job Description:
PAREXEL has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction With...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical Trial Operations
Clinical Trial Operations
PAREXEL International Ltd
0-3 Yrs
14 hrs ago
Hyderabad
Hyderabad
Telangana State
IN
0
Hyderabad
Clinical Trial Operations
12-12-2019
2020-03-11
PAREXEL has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction Within this model the Clinical Site Manager CSM formerly the Clinical Research Associate CRA serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typical clinical monitor CSMs are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success This includes addressing and resolving site issues and questions You will also manage site quality and delivery from site identification through to close-out As a CSM PAREXEL will offer you world class technology and training catered to your individual experience You can anticipate less travel and a lower protocol load in comparison to industry peers Your hard work will be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research If impact flexibility and career development appeal to you please apply to learn more Your Key Accountabilities Act as PAREXELs sole contact with assigned clinical sites Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites generate visit contact report Review the performance of the trial at designated sites ensuring the rights and well-being of human subjects are protected and are in accordance with protocol Evaluate the quality and integrity of the reported data site efficacy and drug accountability Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures SOPs protocol amendment s GCP and the applicable regulatory requirement s Monitor completeness and quality of Regulatory Documentation and perform site document verification Qualifications Your Skillset Site Management experience or equivalent experience in clinical research with understanding of clinical trials methodology and terminology Educated to degree level biological science pharmacy or other health related discipline Demonstrates strong interpersonal written and verbal communication skills within a matrixed team Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight Client focused approach to work flexible attitude with respect to work assignments and new learning Ability to manage multiple tasks to evaluate a variety of unpredictable scenarios and achieve project timelines apply understanding of study protocol s Work ethically and honestly to promote the development of life changing treatments for patients Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System CTMS Electronic Document Management System EDMS and MS-Office products such as Excel and Word Our Offer Join the best minds in the industry and leverage your expertise to help advance treatments into the hands of those who need them most This role is an excellent opportunity to enhance your skills and take the lead on client projects We look forward to speaking with you and determining how PAREXEL fits into your career journey
Full Time
Key Skills :
regulatory, cra, gcp, clinical trials, regulatory documentation...
Job Description:
PAREXEL has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction With...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Oncology
Oncology
PAREXEL International Ltd
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Oncology
12-12-2019
2020-03-11
Parexel has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction Within this model the Clinical Site Manager CSM formerly the Clinical Research Associate CRA serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typical clinical monitor CSMs are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success This includes addressing and resolving site issues and questions You will also manage site quality and delivery from site identification through to close-out As a CSM Parexel will offer you world class technology and training catered to your individual experience You can anticipate less travel and a lower protocol load in comparison to industry peers Your hard work will be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research If impact flexibility and career development appeal to you please apply to learn more Your Key Accountabilities Act as Parexels sole contact with assigned clinical sites Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites generate visit contact report Review the performance of the trial at designated sites ensuring the rights and well-being of human subjects are protected and are in accordance with protocol Evaluate the quality and integrity of the reported data site efficacy and drug accountability Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures SOPs protocol amendment s GCP and the applicable regulatory requirement s Monitor completeness and quality of Regulatory Documentation and perform site document verification Qualifications Your Skillset Site Management experience or equivalent experience in clinical research with understanding of clinical trials methodology and terminology Oncology experience required Knowledge of or strong Interest in Early Phase monitoring required Educated to degree level biological science pharmacy or other health related discipline Demonstrates strong interpersonal written and verbal communication skills within a matrixed team Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight Client focused approach to work flexible attitude with respect to work assignments and new learning Ability to manage multiple tasks to evaluate a variety of unpredictable scenarios and achieve project timelines apply understanding of study protocol s Work ethically and honestly to promote the development of life changing treatments for patients Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System CTMS Electronic Document Management System EDMS and MS-Office products such as Excel and Word
Full Time
Key Skills :
regulatory, cra, gcp, clinical trials, regulatory documentation...
Job Description:
Parexel has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction With...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical Trial Operations
Clinical Trial Operations
PAREXEL International Ltd
0-3 Yrs
14 hrs ago
New York City
New York City
Not Mentioned
IN
0
New York City
Clinical Trial Operations
12-12-2019
2020-03-11
Parexel has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction Within this model the Clinical Site Manager CSM formerly the Clinical Research Associate CRA serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typical clinical monitor CSMs are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success This includes addressing and resolving site issues and questions You will also manage site quality and delivery from site identification through to close-out As a CSM Parexel will offer you world class technology and training catered to your individual experience You can anticipate less travel and a lower protocol load in comparison to industry peers Your hard work will be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research If impact flexibility and career development appeal to you please apply to learn more Your Key Accountabilities Act as Parexels sole contact with assigned clinical sites Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites generate visit contact report Review the performance of the trial at designated sites ensuring the rights and well-being of human subjects are protected and are in accordance with protocol Evaluate the quality and integrity of the reported data site efficacy and drug accountability Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures SOPs protocol amendment s GCP and the applicable regulatory requirement s Monitor completeness and quality of Regulatory Documentation and perform site document verification Qualifications Your Skillset Site Management experience or equivalent experience in clinical research with understanding of clinical trials methodology and terminology Oncology monitoring experience strongly preferred Educated to degree level biological science pharmacy or other health related discipline Demonstrates strong interpersonal written and verbal communication skills within a matrixed team Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight Client focused approach to work flexible attitude with respect to work assignments and new learning Ability to manage multiple tasks to evaluate a variety of unpredictable scenarios and achieve project timelines apply understanding of study protocol s Work ethically and honestly to promote the development of life changing treatments for patients Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System CTMS Electronic Document Management System EDMS and MS-Office products such as Excel and Word Our Offer Join the best minds in the industry and leverage your expertise to help advance treatments into the hands of those who need them most This role is an excellent opportunity to enhance your skills and take the lead on client projects We look forward to speaking with you and determining how Parexel fits into your career journey EEO DisclaimerPAREXEL is an equal opportunity employer Qualified applicants will receive consideration for employment without regard to legally protected status which in the US includes race color religion sex sexual orientation gender identity national origin disability or protected veteran status
Full Time
Key Skills :
regulatory, cra, gcp, clinical trials, regulatory documentation...
Job Description:
Parexel has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction With...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Manager Regulatory Affairs
associate
Manager Regulatory Affairs
Abbott India Ltd
0-3 Yrs
14 hrs ago
United Kingdom, Uk
United Kingdom
,
Not Mentioned
IN
0
United Kingdom
Uk
Not Mentioned
IN
0
Uk
associate
Manager Regulatory Affairs
12-12-2019
2020-03-11
Abbott is a global healthcare leader that helps people live more fully at all stages of life Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medical devices nutritionals and branded generic medicines Our 103 000 colleagues serve people in more than 160 countries Abbott Diagnostics broad range of innovative instruments and tests meets the needs of blood banks and laboratories of all specialties and sizes around the world These products have helped transform the practice of medical diagnosis from an art to a science by greatly contributing to the modern diagnostics industry through our commitment to improving patient care Abbott Diagnostics ADD will be recruiting for an Associate Manager Regulatory Affairs to support UK medical device product registrations Primary Objective of Position Serves as UK Authorized Representative AR Responsible for UK product registrations Identifies and reports new or changed regulations Supports commercial organization with the required Regulatory Documentation Supports product notification in EU countries Acts as EU Regulatory backup Responsible for vigilance reporting of medical device incidents MDI and Field Safety Corrective Actions FSCA and related correspondence to UK competent authorities Major Accountabilities Regulatory Serves as the main contact between the UK authorities and country affiliate Performs product registrations following the UK requirements processes and timings Reviews UK laws regulations and elevates according to ADD elevation process Supports locally developed Ad Promo material review and approval Ensures performance evaluations requirements are met guidance notifications submissions follow-up with authorities and ethic committees Supports customers and tender with RA documentation Generates and maintains RA documents Coordinate its availability with QA organisation Represents RA in the key country trade associations Supports RA activities in the EU EFTA countries as needed Vigilance Vigilance Reports to be reviewed and sent to UK Competent Authority for Abbott Diagnostics ADD and Abbott Molecular AMD products In Vitro Diagnostics Molecular Diagnostics according to shared service agreements Requests from UK Competent Authority to be reviewed and responses to be collected consolidated and submitted according expected time line Follow-up reports to be sent to UK Competent Authority as requested or committed Stay up to date on vigilance related regulation and guidelines applicable for UK and EEA countries Switzerland Support of EU Vigilance team as Vigilance contact back-up for EEA countries Switzerland Education Solid scientific background Degree in Medicine Biology Chemistry or Similar Background Demonstrated experience in regulatory affairs in the diagnostic medical device industry ideally with experience of In Vitro Diagnostics Experience to work in an international work environment or on international projects is required Project management and negotiation skills Ability to work independently Proficient in English Knowledge of PC- and internet based applications Impact of position Operates under Quality and Regulatory directives Follows local regulations and European guidelines for vigilance As youd expect from a global healthcare company we offer a fantastic range of benefits including competitive salaries a superb defined contribution pension scheme private healthcare life assurance and a flexible benefits scheme
Full Time
Key Skills :
regulatory, regulatory affairs, chemistry, regulatory documentation, biology...
Job Description:
Abbott is a global healthcare leader that helps people live more fully at all stages of life Our portfolio of life-changing technologies spans the ...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Meat Cutter
associate
Meat Cutter
associate
WALMART INDIA
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Meat Cutter
associate
12-12-2019
2020-03-11
Location SANTA FE NM Career Area Business Operations Job Function - Employment Type Regular Permanent Position Type Hourly Requisition R-48624 What youll do at Cleans the Meat Department during the course of normal production work for example work surfaces meat grinders windows mirrors display cases and coolers while following Company procedures guidelines and methods and utilizing approved chemicals supplies tools and equipment Provides Meat products to Members by processing meat which includes but is not limited to cutting slicing grinding and wrapping meat for example boneless bone-in products based on Company specifications operating repairing and sanitizing equipment assisting Members with purchasing decisions and ensuring merchandise is properly packaged labeled and stored Provides Member service by acknowledging the Member identifying their needs assisting with purchasing decisions locating merchandise resolving issues and concerns and promoting the Companys products and services Maintains merchandise presentation by stocking merchandise setting up cleaning and organizing product displays removing damaged goods signing and pricing merchandise appropriately and securing fragile and high-shrink merchandise Maintains the Sales Floor in the Meat area in accordance with Company policies and procedures by properly handling claims and returns zoning the area arranging and organizing merchandise and identifying shrink and damages Receives and stocks merchandise throughout the Facility and organizes and maintains Facility by following Company procedures utilizing equipment appropriately merchandising and completing paperwork logs and other required documentation Maintains safety of Facility by following all safety standards procedures and guidelines including conducting safety sweeps following proper forklift spotting procedures following proper procedures for handling and disposing of hazardous materials following Company steel standard guidelines and correcting reporting unsafe situations to Management Follows Company policies and procedures for preparing handling packaging labeling and storing food operating and sanitizing food-related equipment stocking and displaying food products and maintaining and cleaning the Fresh Department Minimum Qualifications Outlined below are the required minimum qualifications for this position If none are listed there are no minimum qualifications I acknowledge that the position for which I am applying requires me to successfully complete all job required trainings and assessments within a prescribed time period if I receive the position Preferred Qualifications Outlined below are the optional preferred qualifications for this position If none are listed there are no preferred qualifications Minimum Qualifications I acknowledge that the position for which I am applying requires me to successfully complete all job required trainings and assessments within a prescribed time period if I receive the position About Sams Club Sam Walton opened the first Sams Club in 1983 to meet a growing need among customers who wanted to buy merchandise in bulk Since then Sams Club has grown rapidly opening more than 600 clubs in the U S and 100 clubs internationally By offering affordable wholesale merchandise to members Sams Club helps make saving simple for families and small business owners Sams Club employs about 110 000 associates in the U S The average club is 134 000 square feet and offers bulk groceries and general merchandise Most clubs also have specialty services such as a pharmacy an optical department a photo center or a tire and battery center
Full Time
Key Skills :
production, documentation, forklift, safety standards, safety...
Job Description:
Location SANTA FE NM Career Area Business Operations Job Function - Employment Type Regular Permanent Position Type Hourly Requisition R-48624 What ...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Senior Clinical
research
associate
Senior Clinical
research
associate
Iqvia
0-3 Yrs
14 hrs ago
Spain
Spain
Not Mentioned
IN
0
Spain
Senior Clinical
research
associate
12-12-2019
2020-03-11
IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients Formed through the merger of IMS Health and Quintiles IQVIA offers a broad range of solutions that harness the power of healthcare data domain expertise transformative technology and advanced analytics to drive healthcare forward IQVIA Biotech has an exciting position within its EU Clinical Monitoring team The Clinical Monitoring department is the largest team within IQVIA Biotech providing CRA Clinical Leads Management and oversight to global clinical studies Were looking for a lively enthusiastic and independent professionals who are willing to work from home with an international EU team Becoming a CRA at IQVIA Biotech doesnt stop with monitoring clinical sites we provide our teams with opportunity and environments to grow and explore their skills We have a culture of developing top talent and taking them to where they want to be be it Project Management Safety Management IQVIA Biotech specialises in working with smaller biotech and emerging biopharma clients and as such we have a vibrant fast-paced work environment Youll be working with a lot of the new innovative and upcoming research groups across a variety of therapy areas BASIC FUNCTIONS Participates in the preparation and execution of Phase I-IV clinical trials Oversees the progress of clinical investigations by conducting site evaluation initiation and interim close out visits to sites Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors Works closely with the Clinical Trial Manager CTM and or Lead CRA t0 ensure all monitoring activities are conducted according to study requirements The Senior CRA may also serve in the Lead CRA role ESSENTIAL JOB FUNCTIONS DUTIES AND RESPONSIBILITIES Participates in the investigator recruitment process Performs site evaluation visits of potential investigators Evaluates the capability of the site to successfully manage and conduct the clinical study Collaborates with the ISS department to coordinate activities with the site in preparation for the initiation of the study Obtains regulatory documentation for successful implementation monitoring and evaluation of clinical trials Works with ISS and site staff to obtain regulatory IRB IEC approval of study specific documents Performs study initiation activities reviewing with the site personnel the protocol regulatory issues study procedures and provides training on completion of the eCRF monitoring activities and study close-out activities Trains site staff on the EDC system and verifies site computer system Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISS Assures adherence to Good Clinical Practices investigator integrity and compliance with all study procedures through on-site monitoring visits Performs validation of source documentation as required by sponsor Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs by using approved IQVIA Biotech sponsor templates and reports Documents accountability stability and storage conditions of clinical trial materials as required by sponsor Performs investigational product inventory Ensures return of unused materials to designated location or verifies destruction as required Reviews the quality and integrity of the clinical data through 1 in house review of electronic CRF data and 2 on-site source verification Works with sites to resolve data queries May review protocols eCRFs study manuals and other related documents as requested by the Clinical Trial Manager and or Lead CRA Serves as primary contact between IQVIA Biotech and investigator coordinates all correspondence ensures timely transmission of clinical data with the study site and technical reporting as requested Performs study close-out visits per the study specific Clinical Monitoring Plan including final investigational product reconciliation and disposition site study file reconciliation data query resolution through to database lock and resolution of outstanding action items Assists with and attends Investigator Meetings for assigned studies Authorized to request site audits due to data integrity concerns Attends study-related company departmental and external meetings as required Ensures internal and study-related trainings are completed per IQVIA Biotech and or study timelines CTMS should always be current with the pertinent site updates contacts Ensures all study deliverables are completed per IQVIA Biotech and study timelines Conducts Field Evaluation Visits and field training of CRA Is IIs and other Sr CRAs Serves as mentor for junior CRAs and those new to the company and or study Performs other duties as requested KNOWLEDGE SKILLS AND ABILITIES Strong knowledge of clinical research process including working knowledge of all functional areas of clinical trials and medical terminology Experience in monitoring and or coordinating clinical trials required Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions Demonstrated ability to form strong functional relationships Excellent presentation organizational and interpersonal skills Ability to interact with all levels of staff to coordinate execute study activities Ability to handle several priorities within multiple complex trials Ability to reason independently and recommend specific solutions in clinical settings Ability to work independently prioritize and work within a matrix team environment Ability to mentor other CRAs and co-monitor as required Knowledge of electronic data capture including basic data processing functions Knowledge of current GCP ICH guidelines applicable to the conduct of clinical research For the Technical CTM role the CRA must have a deep understanding of IQVIA Biotech systems with the ability to learn even more Join Us Making a positive impact on human health takes insight curiosity and intellectual courage It takes brave minds pushing the boundaries to transform healthcare Regardless of your role you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients Forge a career with greater purpose make an impact and never stop learning Job ID R1083441
Full Time
Key Skills :
site evaluation,
research
, clinical data, ich, gcp...
Job Description:
IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients Fo...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Client Data Operations - Analyst /
associate
- Firmwide Operations
Client Data Operations - Analyst /
associate
- Firmwide Operations
Morgan Stanley Pvt Ltd
0-3 Yrs
14 hrs ago
Mumbai
Mumbai
Maharashtra
IN
0
Mumbai
Client Data Operations - Analyst /
associate
- Firmwide Operations
12-12-2019
2020-03-11
Primary Location Americas-United States of America-Maryland-Baltimore Education Level Bachelors Degree Job Other Employment Type Full Time Job Level Non-Exempt Description About us Morgan Stanley is a Global financial services firm and a market leader in investment banking securities investment management and wealth management services Team Profile Shared Service Banking Operations SSBO delivers industry utility solutions by aligning the right functions people processes and tools into 14 core disciplines offering tailored client service levels that are efficient controlled and compliant with regulation The Party Referential Data Team is part of the Global Client and Account Data Operations Team CADO within SSBO and is responsible for the creation and maintenance of Morgan Stanley party reference data for clients issuers and vendors for the duration of the entire business relationship The team is located in Glasgow Baltimore and Mumbai and cover requests globally You will - Create newly acquired parties client issuer and vendor records in the system This involves investigating various approved sources and analyzing various approved documents to determine key attributes required for operational processing as well as financial and regulatory reporting - Maintain the records of existing parties using the same required analysis and due diligence - Processing Corporate Actions such as name changes mergers etc by validating against approved sources identifying pre- and post-notification requirements of sensitive stakeholders processing the actions ensuring all parties sites hierarchies etc are updated based on the Corporate Action Additionally ensuring all obsolete documents are invalidated and replaced with current valid documentation - Additional duties as they regard party referential data attributes - Partner with key business areas and other stakeholders to assure compliance with policies and regulations as well as to review requests for additional processes and data quality rules which may include remediation initiatives based on new regulations or business requirements - Update proprietary systems with information documentation obtained and potentially performing data quality reviews - Maintain a high level of accuracy and data quality standards Qualifications The ideal candidate will have previous experience knowledge within an Operations related environment They will be a confident analytical person with excellent oral and written communication skills In addition the ideal candidate will possess the following attributes - Qualified at degree level or equivalent industry experience - Aptitude to work in a fast-paced environment - Ability to handle volume spikes and prioritize work including ad-hoc requests and projects to meet business demands in a timely manner - Ability to recognize potential risk issues and escalate report on a timely basis - Adaptability and flexibility ability to perform under pressure or in changing environment - Outstanding attention to details and analytical ability - Proficiency in MS Office Excel PowerPoint and Word - Self-driven capable of performing day-to-day activities with minimal guidance and supervision - Ability to influence stakeholders and gain consensus across different groups
Full Time
Key Skills :
documentation, utility, supervision, action, maintenance...
Job Description:
Primary Location Americas-United States of America-Maryland-Baltimore Education Level Bachelors Degree Job Other Employment Type Full Time ...
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INR
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Array
Array-Array
"YEARLY"
associate
Manager
associate
Manager
KONNECTHR EXECUTIVE SEARCH FIRM
5-7 Yrs
14 hrs ago
Noida
Noida
Uttar Pradesh
IN
0
Noida
associate
Manager
12-12-2019
2020-03-11
Associate Manager Regulatory Affairs For Nesea Market 5 - 8 Years Noida Understanding of food safety quality management operations systems Develop request and review supporting technical and non-technical data and documentation from manufacturers technical libraries and various departmental sources Required Candidate profile B Pharm M Pharm Should have handled regulatory procedure for Hong Kong Thailand Malaysia Singapore Indonesia Philippines etc Masters degree in Nutrition Biology Chemistry Food science Master in Pharmacy with 5 to 7 Years Industry experience Certificate course in Regulatory Affairs Salary Not Disclosed by Recruiter Industry Food Processing Functional Area Medical Healthcare R D Pharmaceuticals Biotechnology Role Category Drug Regulatory Affairs Documentation Role Regulatory Affairs Manager Keyskills Food Safety Regulatory Affairs Nesea Market Associate Manager Regulatory Affairs Food Processing regulatory affairs Desired Candidate Profile Please refer to the Job description above Education- UG BVSC - Veterinary Science B Pharma - Pharmacy B Sc - Any Specialization Food Technology Dairy Technology B Tech B E - Any Specialization PG MVSC - Veterinary Science MS M Sc Science - Any Specialization Dairy Technology Food Technology M Pharma - Pharmacy Doctorate Ph D - Advertising Mass Communication Dairy Technology Food Technology Company Profile KONNECT HR EXECUTIVE SEARCH FIRM Top Pharma Company
Full Time
Key Skills :
dairy technology, food processing, documentation,
associate
manager...
Job Description:
Associate Manager Regulatory Affairs For Nesea Market 5 - 8 Years Noida Understanding of food safety quality management operations systems ...
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INR
Array
Array
Array-Array
"YEARLY"
Senior Integration Engineer
Senior Integration Engineer
Nielsen Research Ltd. Co.
5-8 Yrs
14 hrs ago
New York City
New York City
Not Mentioned
IN
0
New York City
Senior Integration Engineer
12-12-2019
2020-03-11
Here at Nielsen were defining Whats Next by bringing together an unmatched diversity of data about people what they watch and how they behave The primary job responsibility will be to lead technical integrations for Nielsens Addressable TV platform with broadcast and cable networks The ideal candidate should have an understanding of broadcast video delivery IP video delivery traffic and automation systems and TV ad delivery RESPONSIBILITIES Provide technical consulting on Nielsen Addressable TV products to internal and external business partners as a recognized technical expert Understand end-to-end air chain paths and workflows for broadcast and cable networks and develop integration plans to successfully implement required technologies Guide clients through the implementation process from pre-sales through launch and post-production including on-site client visits Investigate and analyze verbal and written requests for product enhancements from clients and partners Partner with Product Leadership Client Service and Engineering leadership to translate client needs into innovative solutions while providing ongoing support for multiple accounts running in parallel Provide ongoing status updates on all client activities to internal stakeholders and leadership teams Provide Level 2 technical support to resolve technical issues for existing and future clients Contribute to innovation and intellectual property creation in the Addressable TV space Facilitate the adoption of new technologies into the Nielsen product set Maintain expert-level knowledge of Nielsens Addressable TV technologies and systems including video watermarking and fingerprinting dynamic ad insertion Smart TV and connected device ecosystem and how they are integrated across all platforms and products including the relationships of processes with upstream and downstream teams Active role in maintaining internal and audited documentation Propose conceptual solutions and recommend alterations and enhancements to improve the quality of products and procedures Quickly respond and assist with technical questions within the greater engineering team Provide training coaching technical and business knowledge sharing to other members of the team Work with Client Services Product Tech Strategy and Engineering to provide support ensuring timely response to more complicated customer issues Occasional travel required for client visits less than 20 PERCENT expected travel QUALIFICATIONS Required 5 years industry experience 3 years experience in a client-facing role supporting clients or 3rd party developers 2 years of development engineering or solutions engineering experience particularly in a field related to broadcast and or digital video delivery systems Bachelor of Science in Computer Science Management Information Systems Information Technology or Information Sciences Technical understanding of broadcast air chains including traffic control video ingestion monitoring automation scheduling SCTE and DAI systems Working knowledge with the following Broadcast Digital Server playout technologies ATSC SCTE OTA vs Satellite vs IP distribution General IT Cloud Storage and SFTP JIRA Kanban Confluence Google Suite Experience compiling documentation to guide technical implementation and validation processes Experience supporting in a pre-sale environment Exceptional communication skills both written and verbal Outstanding organizational time management skills and ability to handle multiple priorities and simultaneous work projects Strong analytical and troubleshooting skills Self motivated and able to work with little oversight Experience in developing implementing or maintaining business performance measurement data and reporting results to senior management Desired Understanding of the addressable advertising ecosystem Understanding of Smart TV and Connected Streaming Device technologies and ecosystem Experience with server side APIs deployed in a Cloud environment Understanding of web service technologies and an aptitude for learning new systems technology and processes Experience mentoring training or coaching team members Experience implementing troubleshooting and supporting Internet-based applications web servers and data storage especially AWS Success Factors Able to develop deep expertise in technology solutions Able to explain complex systems and technology to non-technical clients and colleagues Able to build strong working relationships with external clients as well as with Product Leadership and Client Service colleagues within Nielsen Fostering collaboration and teamwork and demonstrating strong personal integrity ABOUT NIELSEN Were in tune with what the world is watching buying and everything in between If you can think of it were measuring it We sift through the small stuff and piece together big pictures to provide a comprehensive understanding of whats happening now and whats coming next for our clients Todays data is tomorrows marketplace revelation We like to be in the middle of the action Thats why you can find us at work in over 100 countries From global industry leaders to small businesses consumer goods to media companies we work with them all Were bringing in data 24 7 and the possibilities are endless See whats next with us at Nielsen Link Copyright 2019 The Nielsen Company All rights reserved LI-MEX Please note this process is being recruited from our Nielsen Recruitment Center NRC based in Mexico City you might be contacted by one of our Recruiters as part of this process ABOUT NIELSEN Were in tune with what the world is watching buying and everything in between If you can think of it were measuring it We sift through the small stuff and piece together big pictures to provide a comprehensive understanding of whats happening now and whats coming next for our clients Todays data is tomorrows marketplace revelation We like to be in the middle of the action Thats why you can find us at work in over 100 countries From global industry leaders to small businesses consumer goods to media companies we work with them all Were bringing in data 24 7 and the possibilities are endless See whats next with us at Nielsen careers nielsen com Nielsen is committed to hiring and retaining a diverse workforce We are proud to be an Equal Opportunity Affirmative Action-Employer making decisions without regard to race color religion gender gender identity or expression sexual orientation national origin genetics disability status age marital status protected veteran status or any other protected class
Full Time
Key Skills :
enhancements, kanban, scheduling, action, documentation...
Job Description:
Here at Nielsen were defining Whats Next by bringing together an unmatched diversity of data about people what they watch and how they behave The...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical Trial Operations
Clinical Trial Operations
PAREXEL International Ltd
0-3 Yrs
14 hrs ago
Netherlands
Netherlands
Not Mentioned
IN
0
Netherlands
Clinical Trial Operations
12-12-2019
2020-03-11
PAREXEL has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction Within this model the Clinical Site Manager CSM formerly the Clinical Research Associate CRA serves as the clinical sites direct point of contact The CSM role offers the opportunity to go beyond the role of a typical clinical monitor CSMs are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success This includes addressing and resolving site issues and questions You will also manage site quality and delivery from site identification through to close-out As a CSM PAREXEL will offer you world class technology and training catered to your individual experience You can anticipate less travel and a lower protocol load in comparison to industry peers Your hard work will be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research If impact flexibility and career development appeal to you please apply to learn more Your Key Accountabilities Act as PAREXELs sole contact with assigned clinical sites Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites generate visit contact report Review the performance of the trial at designated sites ensuring the rights and well-being of human subjects are protected and are in accordance with protocol Evaluate the quality and integrity of the reported data site efficacy and drug accountability Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures SOPs protocol amendment s GCP and the applicable regulatory requirement s Monitor completeness and quality of Regulatory Documentation and perform site document verification Qualifications Your Skillset Substantial Site Management experience or equivalent experience in clinical research with understanding of clinical trials methodology and terminology Educated to degree level biological science pharmacy or other health related discipline Demonstrates strong interpersonal written and verbal communication skills within a matrixed team Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight Client focused approach to work flexible attitude with respect to work assignments and new learning Ability to manage multiple tasks to evaluate a variety of unpredictable scenarios and achieve project timelines apply understanding of study protocol s Work ethically and honestly to promote the development of life changing treatments for patients Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System CTMS Electronic Document Management System EDMS and MS-Office products such as Excel and Word Our Offer Join the best minds in the industry and leverage your expertise to help advance treatments into the hands of those who need them most This role is an excellent opportunity to enhance your skills and take the lead on client projects
Full Time
Key Skills :
regulatory, cra, gcp, clinical trials, regulatory documentation...
Job Description:
PAREXEL has launched a new clinical operating model to drive effectiveness reduce hand-offs and increase employee client and site satisfaction With...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Senior Solution Engineer
Senior Solution Engineer
Nielsen Research Ltd. Co.
5-8 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Senior Solution Engineer
12-12-2019
2020-03-11
The primary job responsibility will be to lead technical integrations for Nielsens Addressable TV platform with broadcast and cable networks The ideal candidate should have an understanding of broadcast video delivery IP video delivery traffic and automation systems and TV ad delivery RESPONSIBILITIES Provide technical consulting on Nielsen Addressable TV products to internal and external business partners as a recognized technical expert Understand end-to-end air chain paths and workflows for broadcast and cable networks and develop integration plans to successfully implement required technologies Guide clients through the implementation process from pre-sales through launch and post-production including on-site client visits Investigate and analyze verbal and written requests for product enhancements from clients and partners Partner with Product Leadership Client Service and Engineering leadership to translate client needs into innovative solutions while providing ongoing support for multiple accounts running in parallel Provide ongoing status updates on all client activities to internal stakeholders and leadership teams Provide Level 2 technical support to resolve technical issues for existing and future clients Contribute to innovation and intellectual property creation in the Addressable TV space Facilitate the adoption of new technologies into the Nielsen product set Maintain expert-level knowledge of Nielsens Addressable TV technologies and systems including video watermarking and fingerprinting dynamic ad insertion Smart TV and connected device ecosystem and how they are integrated across all platforms and products including the relationships of processes with upstream and downstream teams Active role in maintaining internal and audited documentation Propose conceptual solutions and recommend alterations and enhancements to improve the quality of products and procedures Quickly respond and assist with technical questions within the greater engineering team Provide training coaching technical and business knowledge sharing to other members of the team Work with Client Services Product Tech Strategy and Engineering to provide support ensuring timely response to more complicated customer issues Occasional travel required for client visits less than 20 PERCENT expected travel QUALIFICATIONS Required 5 years industry experience 3 years experience in a client-facing role supporting clients or 3rd party developers 2 years of development engineering or solutions engineering experience particularly in a field related to broadcast and or digital video delivery systems Bachelor of Science in Computer Science Management Information Systems Information Technology or Information Sciences Technical understanding of broadcast air chains including traffic control video ingestion monitoring automation scheduling SCTE and DAI systems Working knowledge with the following Broadcast Digital Server playout technologies ATSC SCTE OTA vs Satellite vs IP distribution General IT Cloud Storage and SFTP JIRA Kanban Confluence Google Suite Experience compiling documentation to guide technical implementation and validation processes Experience supporting in a pre-sale environment Exceptional communication skills both written and verbal Outstanding organizational time management skills and ability to handle multiple priorities and simultaneous work projects Strong analytical and troubleshooting skills Self motivated and able to work with little oversight Experience in developing implementing or maintaining business performance measurement data and reporting results to senior management Desired Understanding of the addressable advertising ecosystem Understanding of Smart TV and Connected Streaming Device technologies and ecosystem Experience with server side APIs deployed in a Cloud environment Understanding of web service technologies and an aptitude for learning new systems technology and processes Experience mentoring training or coaching team members Experience implementing troubleshooting and supporting Internet-based applications web servers and data storage especially AWS Success Factors Able to develop deep expertise in technology solutions Able to explain complex systems and technology to non-technical clients and colleagues Able to build strong working relationships with external clients as well as with Product Leadership and Client Service colleagues within Nielsen Fostering collaboration and teamwork and demonstrating strong personal integrity ABOUT NIELSEN Were in tune with what the world is watching buying and everything in between If you can think of it were measuring it We sift through the small stuff and piece together big pictures to provide a comprehensive understanding of whats happening now and whats coming next for our clients Todays data is tomorrows marketplace revelation We like to be in the middle of the action Thats why you can find us at work in over 100 countries From global industry leaders to small businesses consumer goods to media companies we work with them all Were bringing in data 24 7 and the possibilities are endless See whats next with us at Nielsen Link Copyright 2019 The Nielsen Company All rights reserved LI-MEX Please note this process is being recruited from our Nielsen Recruitment Center NRC based in Mexico City you might be contacted by one of our Recruiters as part of this process ABOUT NIELSEN Were in tune with what the world is watching buying and everything in between If you can think of it were measuring it We sift through the small stuff and piece together big pictures to provide a comprehensive understanding of whats happening now and whats coming next for our clients Todays data is tomorrows marketplace revelation We like to be in the middle of the action Thats why you can find us at work in over 100 countries From global industry leaders to small businesses consumer goods to media companies we work with them all Were bringing in data 24 7 and the possibilities are endless See whats next with us at Nielsen careers nielsen com Nielsen is committed to hiring and retaining a diverse workforce We are proud to be an Equal Opportunity Affirmative Action-Employer making decisions without regard to race color religion gender gender identity or expression sexual orientation national origin genetics disability status age marital status protected veteran status or any other protected class Job Type Regular Primary Location Offsite Offsite Secondary Locations Travel Yes 15 PERCENT of the Time
Full Time
Key Skills :
enhancements, kanban, scheduling, action, documentation...
Job Description:
The primary job responsibility will be to lead technical integrations for Nielsens Addressable TV platform with broadcast and cable networks The idea...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Regulatory Project Director
associate
Regulatory Project Director
ASTRAZENECA PHARMA INDIA LTD
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
associate
Regulatory Project Director
12-12-2019
2020-03-11
At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges We do this with the utmost integrity even in the most difficult situations because we are committed to doing the right thing We continuously forge partnerships that help pursue world-class medicines in new ways combining our peoples exceptional skills with those of people from all over the globe As an Associate Regulatory Project Director in Gaithersburg MD youll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients lives Description The Associate Regulatory Project Director ARPD is an experienced regulatory specialist with strong project management capabilities responsible for leading the end-to-end planning coordination and execution of assigned deliverables The ARPD is a key contributor to regulatory submission strategy identifying submission risks and opportunities while leading regulatory applications and managing procedures through approval The ARPD provides regulatory expertise and guidance on procedural and documentation requirementsto GRET GRST and cross-functional teams working flexibly within and across regions to ensure the delivery of business objectives Accountabilities Responsibilities Understand the regulatory framework including regional trends for various types of applications and procedures for small and large molecules across all regions Provide regulatory expertise on procedural and documentation requirements as defined by Health Authorities for assigned deliverable s including Submission delivery strategy of all dossiers and all application types per market and or region Review documents and provide regulatory input e g response documents high level documents study protocols PSRs etc Analysis of regulatory procedures and special designations used during development authorizations and extension of the product Use and share best practices when handling various applications and procedures during interactions with health authorities and in day-to-day work while operating in a highly dynamic environment Lead and or contribute to the planning preparation including authoring where relevant and delivery of both simple and complex submissions throughout the products life cycle from either a global and or regional perspective Lead GRST GRET sub-teams i e Crossfunctional Submission Delivery teams for major submissions NDA MAA or major LCM initiative Develop execute and maintain submission delivery plans submission content plans and proactively provide status updates to designated stakeholders Coordinate the input maintenance and revision in the OPAL project plans for assigned projects and highlight unforeseen changes in resource demand in a timely manner to Lead RPM and line manager Identify regulatory risks and communicate mitigations to Lead RPM and cross functional teams Support operational and compliance activities for assigned deliverables including generating work requests and submission content plans tracking TMF and document management utilizing the support and input of GRO MCs CROs and or alliance partners where relevant May assume assigned responsibilities for routine and non-routine contact with health authorities and marketing companies Provide coaching mentoring and knowledge sharing within the RPM skill group Contribute to process improvement When assigned Lead RPM role ARPD responsibilities to include Lead the GRET Global Regulatory Execution Team Overall accountability for the project management of all GRET deliverables Key member of the Global Regulatory Strategy Team GRST with focus to deliver the GRST product plan submission milestones This is achieved by development and execution of operationally efficient submission delivery plans by GRST and GRET members Identify regulatory risks and risk mitigation strategies for GRET executions and deliverables with input from all team members Drive the GRST and GRET resourcing process Supports Fee forecasting activities Allocate RPM resources to the GRET deliverables Liaise with GPM and other functional project managers Knowledge sharing and RPM development the go-to person for RPM project guidance and support provides and facilitates coaching within between the GRET and GRST When assigned Market Contact role ARPD responsibilities to include Develop maintain and provide RPM with clear concise timely guidance on current priorities and regulatory requirements for assigned market region s to support RPM project deliverables and business tactical strategic decision-making Drive market region knowledge sharing with key stakeholders e g Marketing Companies Regulatory Science Strategy CMC Regulatory Compliance through appropriate meetings networking and communications Provide support across RPM to maintain and continuously improve regulatory consistency and to achieve right first time submissions in assigned market region s Proactively develop close relationships and have appropriate levels of interactive communication with Marketing Company staff for assigned market region s to drive effective 2-way sharing of information and interpretation of regulatory requirements relating to RPM deliverables Coordinate gathering of documentation to support tenders Oversee general Regulatory compliance in assigned markets regions and escalate any compliance issues Minimum Requirements Education and Experience BS MS Degree in Science or related discipline Extensive regulatory experience within the biopharmaceutical industry or experience at a health authority Thorough Knowledge of drug development Strong project management skills Leadership skills including experience leading multi-disciplinary project teams Preferred Experience Managed first wave Marketing Application and or LCM submissions Managed complex regulatory deliverables across projects products Knowledge of AZ Business and processes Skills and Capabilities Excellent written and verbal communication skills Cultural awareness Scientific knowledge sufficient to understand regulatory issues and facilitate scientific discussions Proficiency with common project management e g MS Project and document management tools Ability to work independently and as part of a team Influencing and stakeholder management skills Ability to analyze problems and recommend actions Continuous Improvement and knowledge sharing focused Next Steps Apply today To be considered for this exciting opportunity please complete the full application on our website at your earliest convenience it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity If you know someone who would be a great fit please share this posting with them AstraZeneca embraces diversity and equality of opportunity We are committed to building an inclusive and diverse team representing all backgrounds with as wide a range of perspectives as possible and harnessing industry-leading skills We believe that the more inclusive we are the better our work will be We welcome and consider applications to join our team from all qualified candidates regardless of their characteristics We comply with all applicable laws and regulations on non-discrimination in employment and recruitment as well as work authorisation and employment eligibility verification requirements Save for Later
Full Time
Key Skills :
gpm, documentation, process improvement, planning, maintenance...
Job Description:
At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges We do this with the utmost integrity even i...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
research
Assoc II
research
Assoc II
Baxter India Pvt Ltd
3-5 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
research
Assoc II
12-12-2019
2020-03-11
We believe every person deserves a chance for a healthy life free from illness and full of possibility We see a world full of healing with viable care options available to those with limited choices today We envision new ways of providing physicians pharmacists and nurses with technologies that not only treat chronic diseases but also work to prevent them Were looking for team members who are motivated to learn grow and innovate while making a meaningful difference for millions of people around the world https www youtube com watchv X0h 0ih8MgQ Essential Duties and Responsibilities Employ appropriate scientific techniques to successfully and independently execute routine tasks that are typically significant portions of larger projects With some supervision lead projects within Baxters change control management process from initiation through closure Typical change control projects may include value improvement VIP and manufacturing support initiatives Change Owners assign and prepare impact assessments develop change plans write and execute engineering studies while working closely with manufacturing plants quality regulatory purchasing and various scientific technical groups Effectively communicate project status to team members and management on a regular basis With some guidance make sound technical recommendations regarding projects that are more routine in nature supporting the global manufacturing network involving solution and container products This includes providing recommendations of techniques that would improve existing product processes Generate technical documentation in support of project deliverables and requirements such as protocols reports specifications SOPs and other supporting documents with minimal guidance Contribute to business case cost estimating for VIPs value improvement projects across solution and container products and global manufacturing network Demonstrate ability to apply technical theories and principles to projects within area of expertise Analyze and determine best solutions to non-routine technical design and or research problems with some assistance utilizing established project management tools Qualifications Knowledge of relevant scientific competencies Possess relevant technical writing and computer skills Effectively able to contribute to and lead cross functional project teams globally with moderate scope Demonstrates flexibility as well as the ability to prioritize and complete multiple tasks Ability to objectively assess organize and clearly communicate complex information to project teams and management Interpret available information and make recommendations to resolve technical challenges Appropriately prioritize assignments to meet project schedules Knowledge of and or experience in a regulated industry preferred Education and or Experience Bachelors of Science degree with 3-5 years of related experience Equal Employment Opportunity Baxter is an equal opportunity employer Baxter evaluates qualified applicants without regard to race color religion gender national origin age sexual orientation gender identity or expression protected veteran status disability handicap status or any other legally protected characteristic EEO is the Law EEO is the law - Poster Supplement Pay Transparency Policy Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities If because of a medical condition or disability you need a reasonable accommodation for any part of the application or interview process please send an e-mail to Americas TTA baxter com and let us know the nature of your request along with your contact information
Full Time
Key Skills :
project management, cost estimating, engineering, technical documentation...
Job Description:
We believe every person deserves a chance for a healthy life free from illness and full of possibility We see a world full of healing with viable c...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
First Article Inspections
associate
Engineer
First Article Inspections
associate
Engineer
QuEST Global Engineering Pvt Ltd
2-5 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
First Article Inspections
associate
Engineer
12-12-2019
2020-03-11
13354BR First Article Inspections Associate Engineer Lafayette INDIANA United States Who is QuESTOur goal is to become the most recognized and trusted global engineering partner for our customersFortune 500 companies in the Aerospace Medical Devices Oil Gas Power and Transportation industries We know we can find solutions to their most important technical and business challenges they encounter We arent consultants We help them make their products the most competitive in the world and thats how weve grown to over 11 000 problem solvers from 50 centers around the world We aspire to be a 100-year company which doesnt mean staid and boring but rather we evolve and adapt to create the frontier of the engineering services industry The TeamThe QuEST Domestic Center is made of talented individuals that execute work for multiple Customers This position is for Collins Aerospace support The FAIRs team is responsible for identify manufacturing process flaws ensure that manufacturers are able to produce items that are compliant with specifications improve quality of manufactured items and reduce manufacturing delays and the overall cost of the item The RoleThe successful candidate is expected to perform with delivery excellence Business professionalism is critical as the role will require collaboration with QuEST team members located across the country and customers located across the globe This team member will be an excellent communicator and detail oriented Data integrity is key Our CultureWe just crossed the 21-year mark and despite remarkable growth we have maintained a culture of empowerment at all levelswhat we call intrepreneurial You will be part of the decision making to drive continuous improvements so we can stay happy and healthy as a business in a challenging industry Not everyone is a great fit We will throw you into the deep end with lots of support but if you want to swim you have much opportunity Were not a place where laziness ego or rigid thinking fit in and thats intentional You can do more at this company than you can in twice the time anywhere else We accelerate success you control the throttle and hold the yoke Job Functions Daily tracking of First Article Inspection FAI review statuses team assignment changes to workload in queue approvals and reviews rejected by suppliers Daily updates to several excel worksheets as well as the end point customers Sharepoint site Packages from FAI reviewers will need to be marked for export control Initial FAI check to ensure all documentation is included for the team to begin their first-pass review Generate weekly spreadsheets of FAIs assigned to the team that have not yet been sent by the supplier for review Archive all communications approvals and exported documentation Interact directly with Supply Quality Engineers Field Quality Engineers and Suppliers on a regular basis Develop work instructions to ensure repeatability Work with cross-functional and interdisciplinary teams QualificationsWere excited to talk to you if AS degree in manufacturing or technical field preferred or 2 years of applicable experience 2 years of experience with customer service interaction is preferred Ability to read and understand a blue print Proficient in MS Office tools especially Word and Excel Have attention to detail Possess excellent communication skills both written and verbal Are experienced with data organization and presentation Work well across borders and in a team oriented environment Like to work in a fast paced created environment without a lot of management oversite You are independent and forward facing Location Lafayette IN Travel Less than 10 PERCENT if required by Customer site Reports to Team Lead Contact TAT NA quest-global com Education Type Associate Degree-Manufacturing Science Job Type Full Time-Regular Experience Level Entry Level Total Years of Exp 3-5
Full Time
Key Skills :
associate
engineer, manufacturing, documentation, manufacturing process, aerospace...
Job Description:
13354BR First Article Inspections Associate Engineer Lafayette INDIANA United States Who is QuESTOur goal is to become the most recognized and ...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Loan Operations , Loan Closing
associate
Loan Operations , Loan Closing
associate
CAPITAL ONE FINANCIAL SERVICES CLIENT
1-4 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Loan Operations , Loan Closing
associate
12-12-2019
2020-03-11
At Capital One were building a leading information-based technology company Still founder-led by Chairman and Chief Executive Officer Richard Fairbank Capital One is on a mission to help our customers succeed by bringing ingenuity simplicity and humanity to banking We measure our efforts by the success our customers enjoy and the advocacy they exhibit We are succeeding because they are succeeding Guided by our shared values we thrive in an environment where collaboration and openness are valued We believe that innovation is powered by perspective and that teamwork and respect for each other lead to superior results We elevate each other and obsess about doing the right thing Our associates serve with humility and a deep respect for their responsibility in helping our customers achieve their goals and realize their dreams Together we are on a quest to change banking for good Loan Operations Loan Closing Associate - Boston MA The Loan Closing team in Boston is seeking an Associate Sr Associate Loan Closer who possesses a thorough understanding of the basic principles governing loan documentation and perfection of security interests They will drive the closing process for commercial loan products including documentation gathering submission of necessary paperwork and due diligence work General Responsibilities Drive the closing process for commercial loan products including documentation gathering submission of necessary paperwork due diligence work Identifies the expectations of the customer and takes actions to support the customer experience Demonstrates ability to balance data with other factors when making decisions Work with Relationship Manager Underwriter to gain an understanding of the key structural issues of loan transactions Liaise and coordinate pre-closing requirements with internal and external clients Underwriter Relationship Manager Syndication Desk Borrowers Lenders and with Capital Markets and Risk Operations Review legal documents and advise on funding mechanics and operational requirements as it pertains to internal booking locations regional and currency policies Monitor and administer participations including sending wire transfers and processing payments and fees Articulate and focus within direct sphere of influence and when interacting with outside teams Plans and balances workload Proactively identifies issues opportunities and progresses appropriately Develops and provides guidance to others in team by sharing knowledge and training Can work in an ambiguous environment Remain current on all pending and proposed regulatory changes affecting compliance Assist in cross training of junior associates Accommodate occasional surges in transition volume and have flexibility to deal with last minute changes Receipt and Delivery of Original Collateral to Custodian Basic Qualifications High School Degree GED or equivalent certification At least 1 year of experience with the Loan Closing Process Preferred Qualifications Familiarity with ACBS or Loan IQ Familiarity with Loan Documentation or Legal Documentation Ability to complete tasks in consistent and timely manner Strong written and oral communication skills Strong organizational skills and attention to detail Strong interpersonal skills and professional demeanor Familiarity with Intralinks SyndTrack or other similar applications Strong Word Excel and PowerPoint skills At this time Capital One will not sponsor a new applicant for employment authorization for this position No agencies please Capital One is an Equal Opportunity Employer committed to diversity and inclusion in the workplace All qualified applicants will receive consideration for employment without regard to sex race color age national origin religion physical and mental disability genetic information marital status sexual orientation gender identity assignment citizenship pregnancy or maternity protected veteran status or any other status prohibited by applicable national federal state or local law Capital One promotes a drug-free workplace Capital One will consider for employment qualified applicants with a criminal history in a manner consistent with the requirements of applicable laws regarding criminal background inquiries including to the extent applicable Article 23-A of the New York Correction Law San Francisco California Police Code Article 49 Sections 4901-4920 New York Citys Fair Chance Act Philadelphias Fair Criminal Records Screening Act and other applicable federal state and local laws and regulations regarding criminal background inquiries If you have visited our website in search of information on employment opportunities or to apply for a position and you require an accommodation please contact Capital One Recruiting at 1-800-304-9102 or via email at RecruitingAccommodation capitalone com All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodations For technical support or questions about Capital Ones recruiting process please send an email to Careers capitalone com Capital One does not provide endorse nor guarantee and is not liable for third-party products services educational tools or other information available through this site Capital One Financial is made up of several different entities Please note that any position posted in Canada is for Capital One Canada any position posted in the United Kingdom is for Capital One Europe and any position posted in the Philippines is for Capital One Philippines Service Corp COPSSC Back To Search Results
Full Time
Key Skills :
loan iq, banking, loan operations, loan documentation, loan closing...
Job Description:
At Capital One were building a leading information-based technology company Still founder-led by Chairman and Chief Executive Officer Richard Fairba...
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Monitoring Service
associate
Monitoring Service
associate
Emerson
1-3 Yrs
14 hrs ago
Philippines
Philippines
Not Mentioned
IN
0
Philippines
Monitoring Service
associate
12-12-2019
2020-03-11
Emerson is committed to creating a global workplace that supports diversity and embraces inclusion We attract develop and retain exceptional people in an inclusive environment where all employees can reach their greatest potential We are committed to the ongoing development of our employees because we know that its critical to the success of our company as a truly global entity Our training programs and initiatives focus on end-to-end development from onboarding through senior leadership We provide a wide range of development opportunities including face-to-face and virtual training mentorship and coaching project management and on-the-job training In Customer Support you will be given the opportunity to make a difference by providing consistent high-value added support across different Emerson products and services globally You will be uniquely positioned to expertly provide unmatched solutions that solve the worlds critical problems and bring more value to Emersons customers The Monitoring Service Associate is a key member of the Emerson ProAct Team In this capacity you will have the opportunity to be part of a team of global experts that helps Emerson customers supermarkets convenience stores retail commercial buildings foodservice transportation etc to optimize facilities and operations maintain conditions assets and facilities and manage energy refrigerants and other valuable resources This ultimately leads to supporting our customers by protecting their hard-earned gains and identifying improvement opportunities to help them expand their businesses What you will work on As a Monitoring Service Associate your responsibilities include All service support including Alarm Management functions such as outbound alarm monitoring inbound call handling dispatch and any other service support required Investigation of refrigeration and or HVAC Heating Ventilation Air-conditioning alarms received and diagnosing them based on agreed standards Ensuring immediate delivery of alarm details with accurate documentation by calling or sending an email to external customers Generating and dispatching service work orders of field technicians to troubleshoot onsite concerns What you will need Graduate of any 4-year degree Graduate of any Engineering course may be considered At least 6 months experience of interactive customer service and related functions Background in offshore service operations is an advantage Who we are looking for Excellent English verbal and written communication skills able to communicate clearly and effectively listens actively and able to adapt communication skills appropriately Good interpersonal skills can collaborate well with others willing to take new instructions and work requests Customer focus displays the drive to deliver relevant solutions based on customer need Flexibility willing to work on shifting schedule may include weekend work with scheduled day off to support the business and customers willing to work over time or on rest day over time to support manpower requirement during critical days and or peak season Resilience and Situational adaptability able to effectively and independently function while maintaining a positive energy level in an environment of constantly shifting demands About Emerson At Emerson we are innovators and problem-solvers focused on a common purpose leaving our world in a better place than we found it Each and every day our foundational valuesintegrity safety and quality supporting our people customer focus continuous improvement collaboration and innovationinform every decision we make and empower our employees to keep reaching higher As a global technology and engineering leader we provide groundbreaking solutions for customers in industrial commercial and residential markets Our Emerson Automation Solutions business helps process hybrid and discrete manufacturers maximize production and protect personnel and the environment while optimizing their energy and operating costs Our Emerson Commercial Residential Solutions business helps ensure human comfort and health protect food quality and safety advance energy efficiency and create sustainable infrastructure Emerson a Fortune 500 company with 15 3 billion in sales and 200 manufacturing locations worldwide is committed to helping employees grow and thrive throughout their careers Whether youre an established professional looking for a career change an undergraduate student exploring options or a recent MBA graduate youll find a variety of opportunities at Emerson Join our team and start your journey today
Full Time
Key Skills :
production, safety, manufacturing, heating, innovation...
Job Description:
Emerson is committed to creating a global workplace that supports diversity and embraces inclusion We attract develop and retain exceptional people...
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Initiation Clinical Site Manager II
Initiation Clinical Site Manager II
PAREXEL International Ltd
2-5 Yrs
14 hrs ago
China
China
Not Mentioned
IN
0
China
Initiation Clinical Site Manager II
12-12-2019
2020-03-11
PAREXEL provides monitors with world class technology training resources and limited protocol load You will also be rewarded for your hard work through our CRA bonus incentive program and career advancement opportunities Your Key Accountabilities Perform all clinical monitoring site management activities for assigned projects in accordance with PAREXELs standard operating procedures Act as PAREXELs direct contact with assigned clinical sites and use judgment to assess and ensure overall integrity of study implementation as well as adherence to study protocol Conduct qualification visits QV site initiation visits SIV and monitoring visits MV at assigned clinical sites Good knowledge of applicable clinical research regulatory requirements i e Good Clinical Practice GCP and International Conference on Harmonization ICH guidelines Function as a mentor and role model for other CRA team members Manage clinical monitoring activities including Arranging on-site visits and logistics Establishment of a site recruitment plan in collaboration with site staff during QV Monitoring completeness and quality of Regulatory Documentation Performing site documentation verification Data collection and drug accountability in accordance with ICH GCP guideline Monitoring patient safety on-site and addressing any violations in a timely manner Qualifications Your Skillset Minimum 2 years of monitoring experience in clinical research Educated to degree level biological science pharmacy or other health related discipline Strong working knowledge of EDC systems and IVRS Experience of CTMS preferred Competent in written and oral English and local language Our Offer We offer you a fascinating and diversified insight into PAREXEL and an exciting journey through the world of clinical research You can expect to work with a successful highly-qualified and dynamic team as you develop your individual scientific profile You can also look forward to a flexible working environment and a pleasant atmosphere If you are ready to join PAREXELs Journey please apply
Full Time
Key Skills :
regulatory requirements, ich, cra, gcp, regulatory documentation...
Job Description:
PAREXEL provides monitors with world class technology training resources and limited protocol load You will also be rewarded for your hard work thr...
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INR
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Paralegal
Paralegal
Nielsen Research Ltd. Co.
3-6 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Paralegal
12-12-2019
2020-03-11
RESPONSIBILITIES Work closely with Sales Client Service Consulting Operations Finance and the General Counsel on the preparation and drafting of data licenses technology licenses and other agreements Prepare and review initial drafts of Master Service Agreements Statements of Work and contract amendments based on templates As needed review client-prepared contract drafts for compliance with Legal Department guidelines and NCS corporate policy Manage contract draft changes with internal and external clients review comments and redlines seek and coordinate internal feedback incorporate redlined changes into documents and manage document versions Negotiate contract revisions and as needed provide negotiation assistance to General Counsel in more complex negotiations Assemble documents for execution Draft manage and update contract templates Update contract reports and database systems Perform contract research and interpretation under the supervision of General Counsel and communicate responses as appropriate Other duties and special projects as assigned DESIRED EXPERIENCE Minimum of 3 years work experience in commercial contracts Experience in technology licensing and or data industry extremely helpful Knowledge of US Privacy laws and self-regulatory requirements Experience with project management and process flow a plus POSITION QUALIFICATIONS Has strong references BS BA degree required Paralegal certification an advantage Learns quickly takes responsibility and works both independently and as a contributing team member Demonstrates excellent communication skills with a friendly and professional demeanor Establishes priorities efficiently coordinates work activities and provides quick turnaround without compromising quality ABOUT NCSolutions Were in tune with what the world is watching buying and everything in between If you can think of it were measuring it We sift through the small stuff and piece together big pictures to provide a comprehensive understanding of whats happening now and whats coming next for our clients Todays data is tomorrows marketplace revelation We like to be in the middle of the action Thats why you can find us at work in over 100 countries From global industry leaders to small businesses consumer goods to media companies we work with them all Were bringing in data 24 7 and the possibilities are endless See whats next with us at NCSolutions careers nielsen com
Full Time
Key Skills :
legal, commercial contracts, legal documentation, agreements, drafting...
Job Description:
RESPONSIBILITIES Work closely with Sales Client Service Consulting Operations Finance and the General Counsel on the preparation and drafting of ...
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First Article Inspection
associate
Engineer
First Article Inspection
associate
Engineer
QuEST Global Engineering Pvt Ltd
2-5 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
First Article Inspection
associate
Engineer
12-12-2019
2020-03-11
13356BR First Article Inspection Associate Engineer Lafayette INDIANA United States Who is QuESTOur goal is to become the most recognized and trusted global engineering partner for our customersFortune 500 companies in the Aerospace Medical Devices Oil Gas Power and Transportation industries We know we can find solutions to their most important technical and business challenges they encounter We arent consultants We help them make their products the most competitive in the world and thats how weve grown to over 11 000 problem solvers from 50 centers around the world We aspire to be a 100-year company which doesnt mean staid and boring but rather we evolve and adapt to create the frontier of the engineering services industry The TeamThe QuEST Domestic Center is made of talented individuals that execute work for multiple Customers This position is for Collins Aerospace support The FAIRs team is responsible for identify manufacturing process flaws ensure that manufacturers are able to produce items that are compliant with specifications improve quality of manufactured items and reduce manufacturing delays and the overall cost of the item The RoleThe successful candidate is expected to perform with delivery excellence Business professionalism is critical as the role will require collaboration with QuEST team members located across the country and customers located across the globe This team member will be an excellent communicator and detail oriented Data integrity is key Our CultureWe just crossed the 21-year mark and despite remarkable growth we have maintained a culture of empowerment at all levelswhat we call intrepreneurial You will be part of the decision making to drive continuous improvements so we can stay happy and healthy as a business in a challenging industry Not everyone is a great fit We will throw you into the deep end with lots of support but if you want to swim you have much opportunity Were not a place where laziness ego or rigid thinking fit in and thats intentional You can do more at this company than you can in twice the time anywhere else We accelerate success you control the throttle and hold the yoke Job Functions Daily tracking of First Article Inspection FAI review statuses team assignment changes to workload in queue approvals and reviews rejected by suppliers Daily updates to several excel worksheets as well as the end point customers Sharepoint site Packages from FAI reviewers will need to be marked for export control Initial FAI check to ensure all documentation is included for the team to begin their first-pass review Generate weekly spreadsheets of FAIs assigned to the team that have not yet been sent by the supplier for review Archive all communications approvals and exported documentation Interact directly with Supply Quality Engineers Field Quality Engineers and Suppliers on a regular basis Develop work instructions to ensure repeatability Work with cross-functional and interdisciplinary teams QualificationsWere excited to talk to you if AS degree in manufacturing aeronautical or technical field preferred or 2 years of applicable experience 2 years of experience with customer service interaction is preferred Ability to read and understand a blue print Proficient in MS Office tools especially Word and Excel Have attention to detail Possess excellent communication skills both written and verbal Are experienced with data organization and presentation Work well across borders and in a team oriented environment Like to work in a fast paced created environment without a lot of management oversite You are independent and forward facing Location Lafayette IN Travel Less than 10 PERCENT if required by Customer site Reports to Team Lead Contact TAT NA quest-global com Education Type Associate Degree-Manufacturing Science Job Type Full Time-Regular Experience Level Entry Level Total Years of Exp 3 - 5
Full Time
Key Skills :
associate
engineer, manufacturing, documentation, manufacturing process, aerospace...
Job Description:
13356BR First Article Inspection Associate Engineer Lafayette INDIANA United States Who is QuESTOur goal is to become the most recognized and t...
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associate
Quality Specialist I
associate
Quality Specialist I
Fluor Corporation Pvt. Ltd.
1-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
associate
Quality Specialist I
12-12-2019
2020-03-11
LINXS is seeking a Quality Specialist for the LAX Automated People Mover APM project in Los Angeles The APM is an electric train system on a 2 25 mile elevated guideway with six stations total for Los Angeles International Airport Early works construction began in May 2018 and the system is expected to be open for passenger service in 2023 The construction portion of the contract is valued at over 2 billion This is an entry-level position designed to develop Quality knowledge and ability Assist in the preparation of routine project inspection schedules discipline activity plans for the Quality function and Quality reports internal and external noting non-conformances and verifying effective corrective action Assist the Construction Quality Manager in administering the Project Quality orientation program to ensure that the project teams are familiar with the requirements of the Project Quality Plan including other Quality matters if required Learn the role of Quality inspection staff Assess if directed by senior Quality management the ability of the suppliers to meet the Quality requirements of the project Assist in the maintenance of project Quality records for all phases of the project Execute project Quality work in accordance with approved Activity Plans Prepare Quality input to the Monthly Progress Report and the Project Status Reviews Adhere to and support Projects Health Safety Environmental and Sustainability Policies Other duties as assigned To be Considered Candidates Must be authorized to work in the country where the position is located and be able to interview on site Basic Job Requirements Accredited four 4 year degree or global equivalent in applicable field of study and no required years of work-related experience or a combination of education and directly related experience equal to four 4 years if non-degreed Ability to communicate effectively with audiences that include but are not limited to management coworkers clients vendors subconsultants construction contractors and the general public Industry and Project related technical knowledge necessary to complete the job Ability to learn and apply knowledge of applicable local state province and federal national statutes and guidelines Ability to attend to detail and work in a time-conscious and time-effective manner Ability to learn and utilize web-based project management for tracking quality documentation Proficient in Microsoft office Word Excel Power Point and Outlook Clear driving record and ability to operate a motor vehicle during the execution of work Basic interpersonal and communication skills Preferred Qualifications Accredited four 4 year degree or global equivalent in technical field preferred Ability to function in the field environment of a construction project as needed Knowledge of Heavy Civil Infrastructure construction Degree Required No Requisition Number 120915BR Diverse Workforce We reserve the right to modify or revise the job descriptions in part or in its entirety Reasonable accommodations will be made in accordance with governing law We are an equal opportunity employer that recognizes the value of a diverse workforce All qualified individuals will receive consideration for employment without regard to race color age sex sexual orientation gender identity religion national origin disability veteran status genetic information or any other criteria protected by federal state or local law
Full Time
Key Skills :
project quality, suppliers, quality inspection, inspection, quality manager...
Job Description:
LINXS is seeking a Quality Specialist for the LAX Automated People Mover APM project in Los Angeles The APM is an electric train system on a 2 25 m...
Apply Now
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Vice President of Global Quality Assurance
Vice President of Global Quality Assurance
Electronics for Imaging, Inc
10-13 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Vice President of Global Quality Assurance
12-12-2019
2020-03-11
Vice President of Global Quality Assurance Location Flexible - US or Europe EFI is a global technology company based in Silicon Valley and is leading the worldwide transformation from analog to digital imaging We are passionate about fueling customer success with products that increase competitiveness and boost productivity To do that we develop breakthrough technologies for the manufacturing of signage packaging textiles ceramic tiles and personalized documents with a wide range of printers inks digital front ends and a comprehensive business and production workflow suite that transforms and streamlines the entire production process The Role This new role is an important step towards establishing a global Quality organization supporting our growth plans and continuous process improvements You will be leading the QA function and team defining the future QA strategy and approach for the company products and processes You will be an active part of the senior management operations team helping to set direction lead continuous improvement initiatives tackle supplier shop floor and field process issues and take an active role in the operational strategy This is a hands-on role responsible for QMS implementation investigation of issues successful CAPA implementation and making important judgement decisions You will be responsible for driving quality initiatives across the organization to ensure continuous improvements promoting a positive working environment by communicating clear direction on the quality strategy Implement maintain and lead continuous improvement of the Global Quality Management System including oversight development and approval of documentation related to product launches development and maintenance of quality metrics creation revision review of SOPs administration of change management timely completion of deviations and investigations implementation of corrective and preventive measures etc Oversee document control archiving processes Maintains awareness of current GxP trends and regulatory authority expectations and implements improvements to the global QMS accordingly Responsible for informing management of quality issues in a timely manner Exhibits professionalism and fosters teamwork to create an environment of support that leads to productivity of personnel and ensures GxP compliance The Candidate The position is suitable for someone with a strong background in manufacturing quality with management experience either currently in a similar senior role with the ambition and skills to step up to the next level The person will be a key representative of the company so needs to have strong customer focused and interpersonal skills Essential Skills and Experience ISO 9001 QMS management experience CAPA SPC 8D or 5Why FAIR or PPAP Proven track record in a quality management role in manufacturing Inspection experience including CMM optical systems and various tools Leadership and decision making qualities Customer focused approach High attention to detail Proficient Microsoft Office skills Word Excel Outlook Hands on approach Positive problem solving attitude Requirements BS or BA in Engineering Operations Management or related degrees 10 years of Quality Experience 75 PERCENT Travel LI-BW1 We move quickly with the purposeful intention of solving a problem accomplishing a goal and ultimately making a difference for our customers partners colleagues and shareholders EFI is an Affirmative Action EEO Protected Veteran Disabled Employer
Full Time
Key Skills :
production, manufacturing, action, quality initiatives, implementation...
Job Description:
Vice President of Global Quality Assurance Location Flexible - US or Europe EFI is a global technology company based in Silicon Valley and is lea...
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Clinical Project Manager , Client Services
Clinical Project Manager , Client Services
PAREXEL International Ltd
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Clinical Project Manager , Client Services
12-12-2019
2020-03-11
The Project Manager serves as the primary operational interface between the client and Parexel Informatics RTSM Services responsible for the oversight of timelines milestones and financials during the study lifecycle This position provides tactical management and leadership to project teams to ensure client projects proceeds on time within budget and with quality therefore maintaining and enhancing client satisfaction Key Accountabilities Associate Project Manager includes all Project Manager Responsibilities however support and mentoring is expected to be given as required from their line Leader or mentor Ensures delivery of RTSM Services and or products to clients within expected timelines and budget with quality including resource planning and management Is primary client contact for the study and manages the client relationship May support pre sales process Manages the project timeline regularly sharing this information with internal stakeholders and the client as appropriate Communicates regularly with internal and external team members regarding study status and provides timely notification to all appropriate parties with deviations from timelines and or deliverables Actively identifies manages and mitigates any project risks ensuring appropriate input from all stakeholders maintaining accurate documentation and communicating to internal and external parties as appropriate Identifies inefficiencies with current processes and recommends improvements Manage client expectations effectively Utilizes delegation and negotiation skills with regard to project tasks to obtain maximum productivity and team involvement Facilitates training for clients as required Attends face to face client meetings and investigator meetings as necessary may require travel Responsible for successful completion of project deliverables including but not limited to client signatures and user documentation Ensure compliance with SOPSs and other relevant regulatory body directives Responsible for resolving study issues in a timely proactive and effective manner May assist with department strategies and goals improving processes and procedures Own and drive project financial management to include ensure project profitability contract and invoice progression and change request management Qualifications Skills Maintain a positive results oriented work environment building partnerships and modeling teamwork communicating to the team in an open balanced and objective manner Excellent interpersonal verbal and written communication skills A flexible attitude with respect to work assignments and new learning Critical thinking to evaluate information gathered from multiple sources reconcile conflicts and decompose high-level information into details Affinity for logical thinking as would be applied in a environment Ability to use technical systems Client focused approach to work meeting and exceeding client expectations Acts as a resource for colleagues and staff members when necessary Problem resolution skills ability to analyze and solve a range of simple and complex problems Demonstrates knowledge of the organization processes and clients Works independently may receive a moderate level of guidance and direction Knowledge Experience Relevant work experience preferably in Clinical trials pharmaceutical environment Knowledge of Project Management concepts and approaches Experience of working with a matrix environment Ability to manage multiple varied tasks with enthusiasm Ability to prioritize workload with attention to detail Familiarity with the development lifecycle and testing methodologies Fluent in verbal and written English language Proficient in Microsoft Office including Word PowerPoint and Excel Knowledgeable and experienced in clinical trials pharmaceutical environment Financial acumen Advanced knowledge of PL concepts approaches EEO DisclaimerPAREXEL is an equal opportunity employer Qualified applicants will receive consideration for employment without regard to legally protected status which in the US includes race color religion sex sexual orientation gender identity national origin disability or protected veteran status
Full Time
Key Skills :
associate
project manager, project manager, project management, logical thinking, user documentation...
Job Description:
The Project Manager serves as the primary operational interface between the client and Parexel Informatics RTSM Services responsible for the oversigh...
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INR
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India QA Analyst
India QA Analyst
WM Logistics
4-7 Yrs
14 hrs ago
Indore
Indore
Madya Pradesh
IN
0
Indore
India QA Analyst
12-12-2019
2020-03-11
Equal Opportunity Employer Minority Female Disability Veteran Waste Management WM a Fortune 250 company is the leading provider of comprehensive waste and environmental services in North America We are strongly committed to a foundation of operating excellence professionalism and financial strength WM serves nearly 25 million customers in residential commercial industrial and municipal markets throughout North America through a network of collection operations transfer stations landfills recycling facilities and waste-based energy production projects To enable our business to expand our lead in a market increasingly enhanced by technology Waste Management is undertaking a substantial technology transformation We are seeking talented Information Technology professionals to join the Waste Management team who are motivated to help us transform the way we design build and use technology With your skills and experience we look for you to combine your technical expertise with industry best practices in an effort to align information technology solutions with Waste Management business strategy I Job Summary Under general supervision conducts moderately complex quality assurance tests and analysis to ensure that meets or exceeds specified standards and end-user requirements Performs intermediate development and execution of test cases II Essential Duties and Responsibilities To perform this job successfully an individual must be able to perform each duty satisfactorily Other ancillary duties may be assigned Drafts and revises moderately complex testing documentation including conditions and scripts Executes moderately complex tests according to established plans and scripts documents problems in an issue log and retests corrections to ensure problems are resolved Creates test data files with valid and invalid records to thoroughly test program logic and verify system flow Identifies recommends and implements changes to enhance the effectiveness of quality assurance strategies Assists in planning and scheduling testing III Supervisory Responsibilities This job has no supervisory duties IV Qualifications The requirements listed below are representative of the qualifications necessary to perform the job A Education and Experience Education Bachelors Degree accredited in Computer Science MIS or similar area of study or in lieu of degree High School Diploma or GED accredited and 4 years of relevant work experience Experience Three years of relevant work experience in addition to education requirement B Certificates Licenses Registrations or Other Requirements None required C Other Knowledge Skills or Abilities Required Intermediate knowledge or skills in one or more of the following is required Proficient in all aspects of the development lifecycle in a structured environment and can work with very little direct supervision in a team environment Hands-on experience in developing QA plans and test cases QA methodologies procedures and documentation Quality Center processes and procedures Quick Test Pro QTP automation experience Knowledge and understanding of project planning Communication skills Can write effective test plans and understands test strategy and project risk particularly from a quality perspective Provides functional business process and technical testing services for all and business process development projects and externally developed projects from initiation through to implementation D Other Knowledge Skills or Abilities that Contribute to Success May require intermediate skills in one or more of the following Web application development imaging technology Subject matter knowledge of general business operations HR Finance Various databases applications and technologies including but not limited to Peoplesoft SQL AS400 Toad Visual Basic web applications and Cloud Computing CRM SalesForce ETL Informatica GIS GPS ESP and other reporting tools Is highly motivated proactive and a great team communicator Judgment skills are needed to assess high-risk areas of an application on which to focus testing efforts when time is limited Database testing Load Performance Testing Security Testing V Work Environment Listed below are key points regarding environmental demands and work environment of the job Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the job Normal setting for this job is office setting If this sounds like the opportunity that you have been looking for please click Apply
Full Time
Key Skills :
information technology, qa, security testing, testing, qtp...
Job Description:
Equal Opportunity Employer Minority Female Disability Veteran Waste Management WM a Fortune 250 company is the leading provider of comprehensive...
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Clinical Medical Affairs Program Manager
Clinical Medical Affairs Program Manager
STRYKER INDIA
10-13 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Clinical Medical Affairs Program Manager
12-12-2019
2020-03-11
Strykers Neurovascular division is focused on advancing the practice of less invasive stroke therapies through its Complete Stroke Care solutions The business is dedicated to providing innovative stroke products and services for ischemic and hemorrhagic stroke and committed to providing clinical education and support to help physicians deliver better patient outcomes Products include stent retrievers detachable coils stents balloons guidewires and microcatheters In February 2019 Stryker Corporation NYSE SYK announced that for the ninth consecutive year has been named as one of the 2016 FORTUNE 100 Best Companies to Work For ranking 11 out of 100 If you join our organization will be working to Make Stroke History Stroke is devastating 1 of 20 deaths is from a stroke according to the CDC Watch this video to see how Stryker is making a difference https www youtube com watchv JANFZrpt1Hg Who we want Data translators Highly effective communicators who can transform data findings into recommendations to compose reports and executive level presentations Strategic thinkers People who enjoy analyzing data or trends for the purposes of planning forecasting advising budgeting reporting or sales opportunities Collaborative partners People who build and leverage cross-functional relationships to bring together ideas data and insights to drive continuous improvement in functions Dedicated achievers People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations Effective communicators People who can interpret information clearly and accurately to concisely communicate results and recommendations to stakeholders senior management and cross-functional teams What you will do As a Clinical Medical Affairs Program Manager you will provide advanced scientific writing expertise to the regulatory clinical and other functional area teams ensuring successful preparation of high-quality submission-ready documents and marketing medical materials which includes developing and maintaining Clinical Evaluation Reports CERs addressing Regulatory Body questions requiring clinical data support and collaborating on a number of other clinical and regulatory documents You will serve as the scientific writing content expert for the department You will be the clinical science liaison with internal customers and regulatory agencies regarding product safety and performance Clinical Regulatory Management Serves as medical writing lead on clinical regulatory documents such as those associated with filings and dossiers including writing and maintaining CERs Converts relevant data and information into a form that meets clinical regulatory document requirements Explains data in manner consistent with the target audience s journal congress requirements and or clinical regulatory requirements Coordinates the review approval and other appropriate functions involved in the production of scientific publishing or clinical regulatory projects Collaborate with RA on all phases of regulatory submissions and approvals including clinical document preparation and review the formulation of responses to regulatory agencies and other clinical regulatory documentation Drive a culture of continuous improvement in the Medical Writing processes incorporating new or updating regulatory requirements Medical and Technical Writing Coordinate the completion of clinical science documents including writing study reports Converts relevant data and information into a form that meets clinical regulatory document requirements Explains data in manner consistent with the target audience s journal congress requirements and or clinical regulatory requirements Coordinates the review approval and other appropriate functions involved in the production of scientific publishing or clinical regulatory projects Collaborate with other teams on clinical study reports clinical evidence gap assessments marketing collaterals PMCF reports systematic literature searches publications and other documents that require the evaluation of clinical data and or clinical literature Clinical Evidence Expertise Serves as a subject matter expert within the department for the Global product portfolio develops and maintains in-depth therapeutic knowledge and applies it to the development of well written clinical evidence documents Understands assimilates and interprets sources of information with appropriate guidance direction from product teams and or authors Interprets and explains data generated from a variety of sources including internal external studies research documentation charts graphs and tables Project Management Responsible for effective communication among team members Holds team members accountable to agreed-upon project dates Negotiates with functional areas on project outcomes and deliverables to meet conflicting demands time deliverables etc Communications Management Provide program updates to management Respond to clinical science questions inquiries from internal customers and regulatory agencies Collaborate with cross-functional team to assure high quality and successful project delivery Represents Clinical on cross-functional product development core teams and oversee clinical advisory boards to guide clinical strategy Business Acumen Understand generally the strategic objectives of senior leaders and use those levers to drive program decisions Contribute to strategic growth decisions and initiatives Partners with cross-functional managers in developing functional strategic initiatives What you need A Bachelors Degree in a Scientific discipline required An advanced degree in Biomedical Sciences or technical discipline preferred A PMP PgMP certificate preferred A minimum of 10 years of Clinical Research experience in Medical device or related industry required or possession of an advanced degree with a minimum of 5 years of Clinical Research experience in the Medical device or related industry required Previous Regulatory experience and familiarity with current regulatory agency guidance and regulations including EU MDR and MEDDEV Rev 4 preferred Knowledgeable in clinical operations risk management regulatory submission and US and international guidelines preferred Previous experience with Medical Device industry or related industry experience required Direct experience with medical and or scientific writing within a medical device industry or related industry including Clinical Evaluation Reports CER and post market surveillance PMS reporting required Applied knowledge of project management tools Demonstrated success in a team-based environment Demonstrated interpersonal written and oral communication skills
Full Time
Key Skills :
medical writing, regulatory submission, regulatory documents,
research
, clinical data...
Job Description:
Strykers Neurovascular division is focused on advancing the practice of less invasive stroke therapies through its Complete Stroke Care solutions The...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Director of Materials and Logistics
associate
Director of Materials and Logistics
Goodrich Corporation Ltd
3-5 Yrs
14 hrs ago
Salem
Salem
Tamil Nadu
IN
0
Salem
associate
Director of Materials and Logistics
12-12-2019
2020-03-11
HNC33 US097-Winston-Salem Westpoint 2599 Empire Drive Winston-Salem NC 27103 USA At Collins Aerospace were dedicated to relentlessly tackle the toughest challenges in our industry all to redefine aerospace Created in 2018 through the combination of two leading companies Rockwell Collins and United Technologies Aerospace Systems were driving the industry forward through technologically advanced and intelligent solutions for global aerospace and defense Every day we imagine ways to make the skies and the spaces we touch smarter safer and more amazing than ever Together we chart new journeys reunite families protect nations and save lives And we do it all with some of the greatest talent this industry has to offer We are Collins Aerospace and we hope you join us as we REDEFINE AEROSPACE At Collins Aerospace our Interiors team is focused on innovation safety and cost efficiency But we dont just get people from point A to point B Were committed to making air travel more comfortable connected and secure As a leader in aviation interior products and services were helping airlines and original equipment manufacturers create a positive experience for their customers With offices and manufacturing facilities in more than 12 states across the U S and more than 10 countries around the globe were changing the game of aircraft interiors Are you ready to join our team Role Overview This position manages a department that includes multiple teams led by managers and or supervisors in Materials and Logistics Leads the implementation of control systems implements materials and inventory management strategies and cost-reduction and improvement initiatives Directs long-term complex projects Primary Responsibilities Leads in the implementation of inventory and quality control systems to meet quality standards and operation schedules Implements cost reduction and improvement initiatives to ensure that materials management and logistics deployment are efficient and cost effective Reports inventory management results and proposed solutions to executive leadership Implements materials and inventory management strategies to ensure that the business meets current and future production targets and quality standards Directs highly complex projects to ensure operating objectives are met Provides logistics documentation to establish the range and depth of spares tools test equipment and related manuals to be deployed and stocked Reviews configuration changes to evaluate impact on logistics deployment Plans schedules and manages the efficient movement of material from receiving or the warehouse to production Manages material inventory supplier integration strategies VMI 3PL supermarkets and import export controls Partners with Industrial Engineering on packaging strategies Basic Qualifications This position requires a Bachelors degree in the appropriate discipline and 10 years of relevant experience or an Advanced degree in the appropriate discipline and 8 years of relevant experience In the absence of a degree 14 years of relevant experience is required At Collins the paths we pave together lead to limitless possibility And the bonds we form with our customers and with each other propel us all higher again and again Some of our competitive benefits package includes Medical dental and vision Three weeks of vacation for newly hired employees Generous 401 k plan that includes employer matching funds and separate employer retirement contribution Tuition reimbursement Life and disability coverage And more Apply now and be part of the team thats redefining aerospace every day United Technologies Corporation is An Equal Opportunity Affirmative Action Employer All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability or veteran status age or any other federally protected class Privacy Policy and Terms Click on this link to read the Policy and Terms Note to candidates regarding interview scams Wed like to make it clear that UTC Aerospace Systems never asks candidates for money If youve been approached with a job offer that you suspect may be fraudulent we strongly recommend you do not respond send money or personal information Please report any suspicious activity to Talent Acquisition
Full Time
Key Skills :
production, safety, rockwell, manufacturing, action...
Job Description:
HNC33 US097-Winston-Salem Westpoint 2599 Empire Drive Winston-Salem NC 27103 USA At Collins Aerospace were dedicated to relentlessly tackle the...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Account Executive
associate
Account Executive
Emerson Electric Co India Pvt Ltd
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
associate
Account Executive
12-12-2019
2020-03-11
Support customer proposals and negotiation efforts as required by sales management and system service sales Maintain system service sales offer files including proposal pricing information Maintain all Value Purchasing Agreements and Alliance documentation Assist service sales system sales in order entry process Assist in development and implementation of programs that increase KOB3 revenue in accordance with Inside Sales Stretch objective Work with headquarters marketing and field sales to improve knowledge of Ovation PlantWeb products Increase presentation knowledge and skills to better enhance ability to promote Ovation and Emerson products services and features Assist service sales personnel in the development of WDPF Ovation life cycle programs Work in unison with PWS headquarters and field sales personnel to provide technical product capability and pricing information Interact with customers and PWS personnel to support inquiries resolve problems issues and increase efficiency of overall sales process Orchestrate support Ovation PlantWeb product demos for customer presentations regional user groups and PWS sponsored events Increase knowledge of power plant operator and engineering functions along with plant processes to increase presentation effectiveness Maintain Ovation demo systems to current hardware revision levels Facilitate PATT updates territory business plans and reports as required to support management and sales requirements Develop demonstration skills for Plantweb AMS Foundation Fieldbus and Emerson field devices Organize and support Live Meeting presentations for territory business plans sales training and other business functions Requirements The position requires a BA BSEE ME CH E Computer Science and a minimum of two years experience in process control application engineering field service marketing or sales Work Authorization No calls or agencies please Emerson will only employ those who are legally authorized to work in the United States This is not a position for which sponsorship will be provided Individuals with temporary visas such as E F-1 H-1 H-2 L B J or TN or who need sponsorship for work authorization now or in the future are not eligible for hire Equal Opportunity Employer Emerson is an Equal Opportunity Affirmative Action employer All qualified applicants will receive consideration for employment without regard to sex race color religion national origin age marital status political affiliation sexual orientation gender identity genetic information disability or protected veteran status We are committed to providing a workplace free of any discrimination or harassment If you have a disability and are having difficulty accessing or using this website to apply for a position you can request help by sending an email to idisability administrator emerson com About Emerson At Emerson we are innovators and problem-solvers focused on a common purpose leaving our world in a better place than we found it Each and every day our foundational valuesintegrity safety and quality supporting our people customer focus continuous improvement collaboration and innovationinform every decision we make and empower our employees to keep reaching higher As a global technology and engineering leader we provide groundbreaking solutions for customers in industrial commercial and residential markets Our Automation Solutions business helps process hybrid and discrete manufacturers maximize production and protect personnel and the environment while optimizing their energy and operating costs Our Commercial Residential Solutions business helps ensure human comfort and health protect food quality and safety advance energy efficiency and create sustainable infrastructure Emerson a Fortune 500 company with 17 4 billion in sales more than 20 Innovation Solutions Engineering Centers and 200 manufacturing locations worldwide is committed to helping employees grow and thrive throughout their careers Whether youre an established professional looking for a career change an undergraduate student exploring options or a recent MBA graduate youll find a variety of opportunities at Emerson Join our team and start your journey today
Full Time
Key Skills :
production, safety, manufacturing, action, innovation...
Job Description:
Support customer proposals and negotiation efforts as required by sales management and system service sales Maintain system service sales offer file...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical Medical Affairs Program Manager
Clinical Medical Affairs Program Manager
STRYKER INDIA
10-13 Yrs
14 hrs ago
Washington Dc
Washington Dc
Not Mentioned
IN
0
Washington Dc
Clinical Medical Affairs Program Manager
12-12-2019
2020-03-11
Job Snapshot Employee Type Full-Time Location Washington DC Job Type Clinical Affairs Job ID R425894 Stryker is one of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care The Company offers a diverse array of innovative medical technologies including reconstructive medical and surgical and neurotechnology and spine products to help people lead more active and more satisfying lives We are currently seeking a Clinical Medical Affairs Program Manager to join our Neurovascular Division to be in Fremont CA or remotely anywhere in the US Strykers Neurovascular division is focused on advancing the practice of less invasive stroke therapies through its Complete Stroke Care solutions The business is dedicated to providing innovative stroke products and services for ischemic and hemorrhagic stroke and committed to providing clinical education and support to help physicians deliver better patient outcomes Products include stent retrievers detachable coils stents balloons guidewires and microcatheters In February 2019 Stryker Corporation NYSE SYK announced that for the ninth consecutive year has been named as one of the 2016 FORTUNE 100 Best Companies to Work For ranking 11 out of 100 If you join our organization will be working to Make Stroke History Stroke is devastating 1 of 20 deaths is from a stroke according to the CDC Watch this video to see how Stryker is making a difference https www youtube com watchv JANFZrpt1Hg Who we want Data translators Highly effective communicators who can transform data findings into recommendations to compose reports and executive level presentations Strategic thinkers People who enjoy analyzing data or trends for the purposes of planning forecasting advising budgeting reporting or sales opportunities Collaborative partners People who build and leverage cross-functional relationships to bring together ideas data and insights to drive continuous improvement in functions Dedicated achievers People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations Effective communicators People who can interpret information clearly and accurately to concisely communicate results and recommendations to stakeholders senior management and cross-functional teams What you will do As a Clinical Medical Affairs Program Manager you will provide advanced scientific writing expertise to the regulatory clinical and other functional area teams ensuring successful preparation of high-quality submission-ready documents and marketing medical materials which includes developing and maintaining Clinical Evaluation Reports CERs addressing Regulatory Body questions requiring clinical data support and collaborating on a number of other clinical and regulatory documents You will serve as the scientific writing content expert for the department You will be the clinical science liaison with internal customers and regulatory agencies regarding product safety and performance Clinical Regulatory Management Serves as medical writing lead on clinical regulatory documents such as those associated with filings and dossiers including writing and maintaining CERs Converts relevant data and information into a form that meets clinical regulatory document requirements Explains data in manner consistent with the target audience s journal congress requirements and or clinical regulatory requirements Coordinates the review approval and other appropriate functions involved in the production of scientific publishing or clinical regulatory projects Collaborate with RA on all phases of regulatory submissions and approvals including clinical document preparation and review the formulation of responses to regulatory agencies and other clinical regulatory documentation Drive a culture of continuous improvement in the Medical Writing processes incorporating new or updating regulatory requirements Medical and Technical Writing Coordinate the completion of clinical science documents including writing study reports Converts relevant data and information into a form that meets clinical regulatory document requirements Explains data in manner consistent with the target audience s journal congress requirements and or clinical regulatory requirements Coordinates the review approval and other appropriate functions involved in the production of scientific publishing or clinical regulatory projects Collaborate with other teams on clinical study reports clinical evidence gap assessments marketing collaterals PMCF reports systematic literature searches publications and other documents that require the evaluation of clinical data and or clinical literature
Full Time
Key Skills :
medical writing, regulatory submission, regulatory documents,
research
, clinical data...
Job Description:
Job Snapshot Employee Type Full-Time Location Washington DC Job Type Clinical Affairs Job ID R425894 Stryker is one of the worlds leading m...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical Medical Affairs Program Manager
Clinical Medical Affairs Program Manager
STRYKER INDIA
10-13 Yrs
14 hrs ago
Chicago
Chicago
Not Mentioned
IN
0
Chicago
Clinical Medical Affairs Program Manager
12-12-2019
2020-03-11
Job Snapshot Employee Type Full-Time Location Virtual Missouri Job Type Clinical Affairs Job ID R425894 Stryker is one of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care The Company offers a diverse array of innovative medical technologies including reconstructive medical and surgical and neurotechnology and spine products to help people lead more active and more satisfying lives We are currently seeking a Clinical Medical Affairs Program Manager to join our Neurovascular Division to be in Fremont CA or remotely anywhere in the US Strykers Neurovascular division is focused on advancing the practice of less invasive stroke therapies through its Complete Stroke Care solutions The business is dedicated to providing innovative stroke products and services for ischemic and hemorrhagic stroke and committed to providing clinical education and support to help physicians deliver better patient outcomes Products include stent retrievers detachable coils stents balloons guidewires and microcatheters In February 2019 Stryker Corporation NYSE SYK announced that for the ninth consecutive year has been named as one of the 2016 FORTUNE 100 Best Companies to Work For ranking 11 out of 100 If you join our organization will be working to Make Stroke History Stroke is devastating 1 of 20 deaths is from a stroke according to the CDC Watch this video to see how Stryker is making a difference https www youtube com watchv JANFZrpt1Hg Who we want Data translators Highly effective communicators who can transform data findings into recommendations to compose reports and executive level presentations Strategic thinkers People who enjoy analyzing data or trends for the purposes of planning forecasting advising budgeting reporting or sales opportunities Collaborative partners People who build and leverage cross-functional relationships to bring together ideas data and insights to drive continuous improvement in functions Dedicated achievers People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations Effective communicators People who can interpret information clearly and accurately to concisely communicate results and recommendations to stakeholders senior management and cross-functional teams What you will do As a Clinical Medical Affairs Program Manager you will provide advanced scientific writing expertise to the regulatory clinical and other functional area teams ensuring successful preparation of high-quality submission-ready documents and marketing medical materials which includes developing and maintaining Clinical Evaluation Reports CERs addressing Regulatory Body questions requiring clinical data support and collaborating on a number of other clinical and regulatory documents You will serve as the scientific writing content expert for the department You will be the clinical science liaison with internal customers and regulatory agencies regarding product safety and performance Clinical Regulatory Management Serves as medical writing lead on clinical regulatory documents such as those associated with filings and dossiers including writing and maintaining CERs Converts relevant data and information into a form that meets clinical regulatory document requirements Explains data in manner consistent with the target audience s journal congress requirements and or clinical regulatory requirements Coordinates the review approval and other appropriate functions involved in the production of scientific publishing or clinical regulatory projects Collaborate with RA on all phases of regulatory submissions and approvals including clinical document preparation and review the formulation of responses to regulatory agencies and other clinical regulatory documentation Drive a culture of continuous improvement in the Medical Writing processes incorporating new or updating regulatory requirements Medical and Technical Writing Coordinate the completion of clinical science documents including writing study reports Converts relevant data and information into a form that meets clinical regulatory document requirements Explains data in manner consistent with the target audience s journal congress requirements and or clinical regulatory requirements Coordinates the review approval and other appropriate functions involved in the production of scientific publishing or clinical regulatory projects Collaborate with other teams on clinical study reports clinical evidence gap assessments marketing collaterals PMCF reports systematic literature searches publications and other documents that require the evaluation of clinical data and or clinical literature Clinical Evidence Expertise Serves as a subject matter expert within the department for the Global product portfolio develops and maintains in-depth therapeutic knowledge and applies it to the development of well written clinical evidence documents Understands assimilates and interprets sources of information with appropriate guidance direction from product teams and or authors Interprets and explains data generated from a variety of sources including internal external studies research documentation charts graphs and tables
Full Time
Key Skills :
medical writing, regulatory submission, regulatory documents,
research
, clinical data...
Job Description:
Job Snapshot Employee Type Full-Time Location Virtual Missouri Job Type Clinical Affairs Job ID R425894 Stryker is one of the worlds leadin...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Director - Regulatory Affairs CMC Commercial Biologics
associate
Director - Regulatory Affairs CMC Commercial Biologics
ASTRAZENECA PHARMA INDIA LTD
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
associate
Director - Regulatory Affairs CMC Commercial Biologics
12-12-2019
2020-03-11
This position will provide Regulatory Affairs CMC strategy and tactical elements of regulatory submissions for approved biologic products This role will actively partner with regulatory therapeutic area counterparts to establish alignment with product regulatory strategies and to communicate Regulatory Affairs CMC documentation requirements to team members both internally and externally with a focus on lot distribution reports This manager position is specifically responsible for providing support in the collection evaluation preparation and assembly of documentation required for US and international ex-US submissions to support both original marketing applications and maintenance of existing licenses for marketed products Assist in the preparation of regulatory submissions including formatting and compilation of submission documentation and preparation of regulatory components forms cover letter etc Assist with the establishment of submission timelines and management of information required to meet submission target dates Responsible for upload retrieval and maintenance of documents for electronic submissions using the appropriate and applications Ensure proper maintenance and filing of regulatory related documentation and track regulatory commitments submission requests timelines and deliverables Research relevant information regulations and guidance from different regulatory agencies Interact with cross-functional groups and attend team meetings as necessary to support submission development and project coordination Assist in the preparation of agendas presentations and other supporting materials for various meetings Author regulatory SOPs Guidelines and Toolkits Provide management updates and project reports as required Assist senior regulatory staff in collating and addressing regulatory submission review comments Review submission documentation for accuracy and compliance with applicable regulations and guidelines as required Support senior regulatory staff in performing regulatory review and evaluation of CMC changes that may impact existing or pending international regulatory files Proactively identify potential issues and alert supervisor for further action Essential BS MS in a scientific discipline Ability to multi-task excellent planning and organizational skills with attention to detail and accuracy Strong interpersonal and communication oral and written skills Computer savvy competent with common computer applications such as MS Word Acrobat PowerPoint Project and Excel and comfortable working with document management and other electronic submission systems Self-motivated and require minimum supervision when performing routine job functions Eager to learn relevant scientific knowledge and new regulatory requirements Desirable Experience working with approved biologics is preferred Experience with firstdoc based documentation management systems Quality Assurance experience orTechnical experience in the testing or manufacture of biotechnology-derived products or complex biologics AstraZeneca embraces diversity and equality of opportunity We are committed to building an inclusive and diverse team representing all backgrounds with as wide a range of perspectives as possible and harnessing industry-leading skills We believe that the more inclusive we are the better our work will be We welcome and consider applications to join our team from all qualified candidates regardless of their characteristics We comply with all applicable laws and regulations on non-discrimination in employment and recruitment as well as work authorisation and employment eligibility verification requirements
Full Time
Key Skills :
supervision, action, documentation, planning, maintenance...
Job Description:
This position will provide Regulatory Affairs CMC strategy and tactical elements of regulatory submissions for approved biologic products This role w...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Sr. Analyst
Sr. Analyst
Nielsen Research Ltd. Co.
3-6 Yrs
14 hrs ago
Chicago
Chicago
Not Mentioned
IN
0
Chicago
Sr. Analyst
12-12-2019
2020-03-11
ABOUT THIS JOB When you see an ad on TV a sponsored post in your social media newsfeed a billboard from the highway or price discount on the shelf do you ever wonder how the advertiser decided to place those ads and whether they actually work to drive purchases If you work at Nielsen you can help advertisers understand the answers to these very important questions and inform their strategies going forward Globally industry spends 600B on advertising and you can become part of the team on a mission to measure improve the efficiency of every single dollar of that spend translating into 60B in value Nielsen is the largest market research firm in the world tracking what people watch and buy-in over 100 countries The consumers world is changing at an unprecedented speed where media and commerce are colliding At Nielsen we are focused on providing our clients with usable practical and meaningful tools that help them make strategic business decisions every day RESPONSIBILITIES Responsible for establishing strong client relationships to drive client retention and be seen as a knowledge resource Understand how client strategic objectives and priorities can be addressed by Nielsen Lift and Marketing Mix solutions in order to drive value to clients Work with manager to design analytic studies that meet advertisers research objectives Consistently develop high-quality decks to report a compelling data story pro-actively share consultative guidance and present to clients collaborate with manager as needed Develop recommendations based on the insights derived from the analysis Present findings and recommendations to clients Leverage technical knowledge of Nielsen Lift and Marketing Mix to effectively explain methodology behind key analytics to clients Provide subject matter expertise to both the client and internal team Develop team process and training documentation as needed to ensure consistency of execution Identify opportunities to collaborate with other Nielsen teams to provide holistic support to clients A LITTLE BIT ABOUT YOU As part of Nielsens Marketing Effectiveness practice you will work with advertisers to help assess how well their marketing activities are working to drive sales and how they should most effectively use their budget in the future Youll be an important partner to well-known consumer-focused companies spanning across several industries including consumer packaged goods retailers technology financial services and telecom You will be expected to work with cross-functional teams to understand and analyze the impact of marketing activities and simulate the impact of future budget changes to help advertisers decide how much to spend on marketing and in what ways to maximize the impact of their spend QUALIFICATIONS Bachelor degree required advanced degree preferred 3 years of marketing research or analytics experience Strong communication and presentation skills Enjoy being hands-on with data and analysis Enthusiasm for applying statistical analysis to address business issues Comfortable working with large data sets Well-organized and detail-oriented capable of handling several projects at a time while meeting deadlines Experience with Nielsen or IRI data a plus ABOUT NIELSEN Were in tune with what the world is watching buying and everything in between If you can think of it were measuring it We sift through the small stuff and piece together big pictures to provide a comprehensive understanding of whats happening now and whats coming next for our clients Todays data is tomorrows marketplace revelation We like to be in the middle of the action Thats why you can find us at work in over 100 countries From global industry leaders to small businesses consumer goods to media companies we work with them all Were bringing in data 24 7 and the possibilities are endless See whats next with us at Nielsen careers nielsen com Nielsen is committed to hiring and retaining a diverse workforce We are proud to be an Equal Opportunity Affirmative Action-Employer making decisions without regard to race color religion gender gender identity or expression sexual orientation national origin genetics disability status age marital status protected veteran status or any other protected class Job Type Regular Primary Location Chicago Illinois Secondary Locations NY - New York City Travel No Nearest Major Market Chicago
Full Time
Key Skills :
workforce, training documentation...
Job Description:
ABOUT THIS JOB When you see an ad on TV a sponsored post in your social media newsfeed a billboard from the highway or price discount on the shel...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Senior
associate
, Quality Control
Senior
associate
, Quality Control
Boehringer Ingelheim India Pvt Ltd
2-6 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Senior
associate
, Quality Control
12-12-2019
2020-03-11
Senior Associate Quality Control - 1916512 Boehringer Ingelheim Fremont is the rapidly growing US arm of Boehringer Ingelheims Biologics Business Unit We are a fully integrated biologics operation with over 500 scientist and specialists covering cutting edge early- to late stage CMC development clinical and commercial drug substance and drug product manufacturing medical device assembly for combination products and packaging operations We are continuing our rapid growth investing over 200m into the expansion of our capacity and capabilities and creating approximately 200 new jobs Driving this growth is an exciting pipeline of multiple Boehringer Ingelheim novel biologic entities NBEs and biosimilars as well as a growing diverse portfolio of therapeutics we develop and manufacture for other leading pharma and biotech companies This includes multiple commercial product launches planned over the next couple of years for which we can tap into Boehringer Ingelheims unique experience of having brought 30 biologics to market globally Leveraging our diverse talent pool we are also driving technology and innovation globally through major investment and collaborations into next generation manufacturing platforms and technologies which may change how biologics will be made in the future Whether we work on our own products help partners to bring their products to market or innovate new technologies and approaches - Everything we do we do to help patients LI-SS1 I-SF1 Description Responsible for providing analytical testing support by conducting cGMP assays for release stability validation and in-process samples Responsibilities include conducting analytical testing per approved SOPs and methods analyzing and reporting data and maintaining lab equipment Report aberrant results to supervisor and assist in lab investigations as required Generate new and or revise analytical SOPs and methods Maintain laboratory cleanliness and orderliness Perform all lab operations in a safe and compliant manner Identifies problems and generates alternatives and recommendations to resolve problems Incumbent coordinates and conducts reviews and investigations in situations involving deviations of product quality from governing procedures processes and regulations assists with on-the-job training for junior-level staff and serves as a resource to them on technical or process questions As an employee of Boehringer Ingelheim you will actively contribute to the discovery development and delivery of our products to our patients and customers Our global presence provides opportunity for all employees to collaborate internationally offering visibility and opportunity to directly contribute to the companies success We realize that our strength and competitive advantage lie with our people We support our employees in a number of ways to foster a healthy working environment meaningful work diversity and inclusion mobility networking and work-life balance Our competitive compensation and benefit programs reflect Boehringer Ingelheims high regard for our employees Duties Responsibilities Analytical Testing Under minimal supervision performs testing conducts lab investigations problem-solves provides supervision of product testing and reports aberrant results to management Under minimal supervision performs required cell and or reagents qualifications Performs Quality Control Biochemistry Testing Group eg HPLC CE PCR Bioassay ELISA and Physico-Chemical in a timely manner Follows well-defined and established procedures and best practices Reviews and approves QC test results in a timely manner Documentation Generates reviews and or maintains records or documents in a detailed and consistent manner Ensure all equipment use logs are recorded for assays performed Assists with QCs data management including data review assay monitoring e g invalid test log and control chart log Process improvement and compliance Coordinates and manages continuous improvement projects Revises standard operating procedures training manuals etc which are submitted to management for adjustments and final approval Maintains specific QC files and database records for process and or quality improvement efforts Actively support cross functional teams and share information as appropriate with colleagues Effectively communicate with supervisors colleagues and or managers in other departments and sites Participate in method validation and method transfer activities Demonstrate troubleshooting and critical thinking skills Highly productive attention to detail ability to manage own time and prioritize tasks independently to meet time lines Maintain laboratory cleanliness and orderliness Dispose expired chemicals timely ensure all equipment is within calibration and or qualification dates and resolve any malfunction issues through appropriate SOPs Ensure that training is up-to-date and other personal development programs are in place Requirements Bachelors degree in Biochemistry Chemistry or Biology is required Demonstrates strong interpersonal and communication skills both written and oral a strong customer focus and an ability to interact with various departments and levels Demonstrates ability to work independently and as part of a team to meet departmental facility goals is also able to work across functions to achieve common goals Demonstrates strong attention to detail and an ability to focus on details of execution Demonstrates ability to work effectively on problems of a diverse scope and with analysis evaluation of data Demonstrates good facilitation organizational and problem solving skills as well as demonstrated technical expertise Expertise is required in HPLC and CE The required expertise is with respect to demonstrating theoretical understanding and providing effective analytical troubleshooting Five 5 years experience with cGMP is required Experience is required in conducting analytical investigations for Out of Specification or Out of Trend Results in accordance with regulatory guidelines Experience in trending analytical data method data and product data is preferred Direct experience is required in method qualification method transfer and method validation in accordance with ICH guidelines Direct experience is desired in participating and supporting regulatory inspections through explanations of methodologies investigations and or laboratory systems Experience in method development is desired Knowledge of and the ability to implement CFR USP and ICH requirements is desired Knowledge of LIMS ELISA i e Softmax Pro and luminometer is required Ability to implement and demonstrate testing in accordance 21CFR11 is required Eligibility Requirements Must be legally authorized to work in the United States without restriction Must be willing to take a drug test and post-offer physical if required Must be 18 years of age or older
Full Time
Key Skills :
manufacturing, action, documentation, cgmp, process improvement...
Job Description:
Senior Associate Quality Control - 1916512 Boehringer Ingelheim Fremont is the rapidly growing US arm of Boehringer Ingelheims Biologics Business Un...
Apply Now
INR
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"YEARLY"
Customer Service
associate
-VCS
Customer Service
associate
-VCS
AMAZON INDIA PVT LTD
0-3 Yrs
14 hrs ago
Jaipur
Jaipur
Rajasthan
IN
0
Jaipur
Customer Service
associate
-VCS
12-12-2019
2020-03-11
Customer Service Associate-VCS Job ID 664337 ADCI - Rajasthan DESCRIPTION An Amazon Customer Service Associate is a critical part of our mission to deliver timely accurate and professional customer service to all Amazon customers This vital position requires an action-oriented flexible problem-solver who will assist customers in expediting orders and correcting post-sales problems Associates communicate with customers primarily through mail chat and phone and utilize a variety of tools to navigate customer accounts research and review policies and communicate effective solutions in a fun and fast-paced environment Virtual Customer Service VCS - It is a Work from Home model for India CS VCS associates are expected to work from a home location approved by Amazon for all scheduled hours It is the responsibility of the associates to ensure uninterrupted internet connectivity and work-like environment at home location so that associates can deliver their best in terms of productivity and quality BASIC QUALIFICATIONS Minimum qualification is 10 2 Any graduate PG is eligible to apply PREFERRED QUALIFICATIONS Communication Skills Excellent communications skills Written and verbal Ability to communicate correctly and clearly with all customers Excellent documentation skills Good comprehension skills ability to clearly understand and state the issues customers present Ability to concentrate follow customer issue without distraction to resolution Good composition skills ability to compose a grammatically correct concise and accurate written response Work successfully in a team environment as well as independently Computer knowledge Skills Ability to use a desktop computer system Familiarity with Windows XP Microsoft Outlook Microsoft Word and Internet Explorer Excellent typing skills Demonstrable understanding of the Internet Amazon com website and competitor websites Demonstrates an ability to successfully navigate websites Demonstrates a proficient knowledge of email applications Demonstrates an ability to learn in various media Ability to successfully adapt to changes in their environment Customer Focus Excellent customer service skills including maintaining focus on the customer issue amidst a bustling fast-paced environment Ability to empathize with and prioritize customer needs Demonstrable interpersonal skills with a diverse customer base Demonstrable conflict resolution negotiating and de-escalation skills Demonstrate ownership to resolve challenging customer issues escalating when necessary Ability to determine customer needs and provide appropriate solutions Maintain regular and reliable attendance including daily schedule as assigned Flexible with working schedule may be expected to work weekends holidays and events Ability to work overtime as dictated by business need as much as 60 hours a week most often occurring in the weeks surrounding the Christmas holiday season Problem Solving Skills Effective problem solving skills including decision making time management immediate prioritization of tasks as assigned Ability to approach problems logically rationally Action oriented and self disciplined Organized and detail oriented Ability to quickly effectively prioritize work time in various departments to meet business need Ability to maintain composure in highly escalated situations Qualified candidates will be comfortable in a multi-tasking high-energy environment They will be creative and analytical problem solvers with a passion for excellent customer service Job details IN RJ Jaipur Customer Service Technical and Non-Technical Teams Customer Service
Full Time
Key Skills :
policies, conflict resolution, time management, decision making, attendance...
Job Description:
Customer Service Associate-VCS Job ID 664337 ADCI - Rajasthan DESCRIPTION An Amazon Customer Service Associate is a critical part of our mission t...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
research
associate
research
associate
j mitra and company private ltd.
2-5 Yrs
14 hrs ago
Delhi, Ncr
Delhi
,
Delhi
IN
0
Delhi
Ncr
Not Mentioned
IN
0
Ncr
research
associate
12-12-2019
2020-03-11
Research Associate Delhi- J Mitra Co Pvt Ltd 0 - 2 Years Delhi Purpose of Position The purpose of the position is to assist the HOD in the planning organizing and conducting of Research Analysis and to ensure timely completion of allotted assignment and projects Job Responsibilities Planning organizing and conducting Research Analysis and trouble shooting in the assigned projects processes Documentation of observations analysis of experiments and interpretation of results In continuation to same preparation of summary and further planning and execution work for the completion of delegated projects assignments Meeting deadlines for the timely completion of projects assignments Assisting in the setup operations maintenance and Calibration Validation of lab equipments instruments and simultaneously maintain the records documents to comply with regulatory requirements Maintenance of inventory of material on a regular basis Assisting seniors in administrative tasks Any other task assigned by the Reporting Manager The Job responsibilities may be revised as per company requirements as and when required Required Candidate profile Educational Qualification Required Min MSC Biotechnology Biochemistry Desired PHD Fresher 02 years of experience in lab Perks and Benefits
Full Time
Key Skills :
iso, documentation, planning, instruments, maintenance...
Job Description:
Research Associate Delhi- J Mitra Co Pvt Ltd 0 - 2 Years Delhi Purpose of Position The purpose of the position is to assist the HOD in t...
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INR
Array
Array
Array-Array
"YEARLY"
Legal
associate
Legal
associate
MY UNNATI
1-3 Yrs
14 hrs ago
Roorkee, Noida, Gurgaon, Delhi, Ncr
Roorkee
,
Not Mentioned
IN
0
Roorkee
Noida
,
Uttar Pradesh
IN
0
Noida
Gurgaon
,
Haryana
IN
0
Gurgaon
Delhi
,
Delhi
IN
0
Delhi
Ncr
Not Mentioned
IN
0
Ncr
Legal
associate
12-12-2019
2020-03-11
We have got an opportunity for you to work with the fastest-growing legal technology company and be part of an awesome team Our client is an online platform for legal information and advice The users can post anonymous questions and receive legal advice from expert lawyers also they can book consultations with the lawyer that suits their requirement for a minimal fee The founders are IIT Roorkee alumni who although from a tech background understood exactly what trouble Indians go through to resolve their legal queries and issues Started out in 2015 their team helps people across property issues medical negligence divorce child custody immigration cheque bounce cases consumer cases legal drafting intellectual property disputes fundraising for startups amongst others As a Legal Associate you will be responsible for defining strategy structuring and streamlining processes to cater best in class services for lawyers and corporates What you will do Preparing standardized processes for internal functions with respect to the concerned industry corporate clients and field of practice Preparing templates of legal documents with the aim of reducing human effort with the help of technology Responsible for drafting vetting reviewing legal documents and preparing and advising on the necessary checklist to be adopted to ensure information is submitted on time Providing advisory opinions to Clients on a versatile array of legal issues pertaining to various disputes Executing legal research with precision and proficiency in arguments Reviewing the service delivery to the clients and coordinating with the lawyer law firm for the same Preparing criteria and qualifiers for enriching the deliverables to the client Required Candidate profile What you need to have Excellent written verbal communication presentation skills Negotiation Time Management and Planning Skills Problem solving analytical and diagnostic skills Ability to work individually and as part of a team Must be able to perform successfully in a fast-paced intellectually intense service-oriented environment and to interpret rules and guidelines flexibly to enhance the business and in keeping with Companys values policies and procedure Should be from legal background Keyskills Legal Documentation Legal Advice Fund Raising Vetting Intellectual Property Legal Drafting Property Disputes Consumer Cases Suits Lawyer Activities Desired Candidate Profile Please refer to the Job description above Education
Full Time
Key Skills :
vetting, legal manager, legal advice, legal, property...
Job Description:
We have got an opportunity for you to work with the fastest-growing legal technology company and be part of an awesome team Our client is an online...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Technician III
associate
Technician III
Abbott India Ltd
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
associate
Technician III
12-12-2019
2020-03-11
Abbott is a global healthcare leader that helps people live more fully at all stages of life Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medical devices nutritionals and branded generic medicines Our 103 000 colleagues serve people in more than 160 countries Position Summary This position provides technical support by performing any combination of routine or occasional non-routine duties involving the selection and use of standard procedures and or equipment in support of medical diagnostic instrument and or reagent development and production Main Responsibilities Applies a high level of technical support working in a specialized discipline such as electronics life science chemistry mechanics etc Understands and uses knowledge of other disciplines Uses computer applications as needed for functional specialty Basic skills in computer hardware and or applications such as spreadsheet creation Accepts non-routine and complex assignments Follows established procedures Uses judgment and makes choices on how to proceed Uses information from within and or outside the organization when necessary Reads interprets and may instruct others in the use of all manuals test procedures and documentation associated with specialized equipment Reads and interprets engineering drawings schematics and complex test procedures Drafts basic procedures and technical documents Working knowledge and use of complex tools and equipment specific to functional areas May use statistical mathematical and other quantitative and qualitative methods and measurements Conducts failure analysis to component level Conducts complex testing analysis and troubleshooting May conduct basic experimental design in functional areas May analyze new products or new applications of existing products Recommends changes for process improvement Complies to all safety standards and regulatory requirements Accountability Problem Solving Resolves complex problems with data gathering research analysis and interpretive activities Uses factual information policy and procedures to determine solutions with minimal supervision Impact on Operations Effect of Errors Tasks activities and or information used to make decisions which are in direct support of the departments primary function Effect of errors may have significant impact in terms of time or money Qualifications High School or equivalency is required Technical certificate or Associates degree is preferred This position requires three to five or more years related technical experience Training includes on the job training Degree of physical effort and environment Normal work fatigue Normally safe environment Typical electronic manufacturing laboratory office environment Some work subject to frequent hand eye coordination lifting carrying of objects or operating equipment Work may be subject to moderately unpleasant conditions Applies to biohazard environment only
Full Time
Key Skills :
production, failure analysis, lifting, supervision, manufacturing...
Job Description:
Abbott is a global healthcare leader that helps people live more fully at all stages of life Our portfolio of life-changing technologies spans the sp...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
research
Scientist
research
Scientist
Abbott India Ltd
7-10 Yrs
14 hrs ago
Mumbai
Mumbai
Maharashtra
IN
0
Mumbai
research
Scientist
12-12-2019
2020-03-11
Job Title Research Scientist Formulation Job Function Innovation Development Location Mumbai Reporting to Group Leader Formulation Purpose Deliver formulations in defined timeframe to meet product delivery goals for I D Development of different formulations either as generic or differentiated generics To demonstrate successful stability and scale up at manufacturing site Core Job Responsibilities Development of formulation using scientific rationale in use of excipients to create a reproducible prototype formulation Ensure Proper documentation of every trial in the log note books and then using the information for creation of the Product Development Report for use in dossier for filing Use of QbD wherever required for Product and process optimization Ensure proper upkeep maintenance and calibration of the equipment Ensure scale up of the developed formulation works at engineering batch level Development of the patent non-infringing strategy for product development Preparation of regulatory documents for PK study and marketing approval from DCG I Preparation of Pharmaceutical Development report for Quality module of CTD Key Deliverables Literature Patent search to create drug profile Prototype development with rationale use of excipients Pre-formulation study as may be required for formulation development Conduct 6 months accelerated stability studies to ensure stable formulation Proof of concept studies to demonstrate BE or comparative PK as the case may be Scale up studies at 1 10th scale or engineering batch Technology transfer and manufacturing of Bio Clinical batch Critical Success Factors Functional Technical Formulation and Product Development Schedule and follow all the steps to deliver the drug as per QTPP Select the suitable polymers excipients based on either properties or scientific rationale Evaluation of CQA of drug excipients and estimate its implications for product development Designs the process which is reproducible and scalable with higher yield cost effective and environment friendly Plan and executes the trial to identify Critical Process Parameters CPP and design the control strategy Overcomes the limitations problems and effectively resolves the same Design of Experiments Plans and executes the experiments as per DOE to optimize product and process Applies basic principles of experimentation Pharmaceutical Development Report PDR Prepares PDR as per Common Technical Document CTD module 3 requirements Complies with regulatory requirements as defined in QTPP Project Management Is able to plan and prioritize multiple project deadlines to meet product delivery goals Education experience M Pharm Ph D 7 - 10 yrs JOB FAMILY Product Development
Full Time
Key Skills :
group leader, process optimization, prototype development, product development, manufacturing...
Job Description:
Job Title Research Scientist Formulation Job Function Innovation Development Location Mumbai Reporting to Group Leader Formulation Pur...
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INR
Array
Array
Array-Array
"YEARLY"
Legal Consultant
Legal Consultant
RIYADH CABLES GROUP OF COMPANIES
10-13 Yrs
14 hrs ago
United Arab Emirates, Uae
United Arab Emirates
,
Not Mentioned
IN
0
United Arab Emirates
Uae
Not Mentioned
IN
0
Uae
Legal Consultant
12-12-2019
2020-03-11
Within the mission vision and values of Riyadh Cables Group of Companies provides legal advice and opinion on all legal issues especially on contracts and torts and providing drafting of all legal documents The legal consultants main objective is to provide assistance in all the legal matters and advise in legal documentation negotiations contracts etc This professional is responsible for defending the rights and the legitimate interests of Riyadh Cables Group of Companies The consultant is responsible for drafting and reviewing the legal filings and drafting technically correct opinions The consultant is responsible for maintaining client relationships and conducts new research work as well The legal consultant may work in different areas and the duties of this professional will differ accordingly and as per the needs of Riyadh Cables Group of Companies Requirements B Sc in Law or equivalent 10 years of experience Well knowledge of the Saudi labor law and workers and Saudi governmental procedures Good verbal and written communication skills in English and Arabic Successful candidates should possess the following Supports the organizations program by providing Risk Management assessment evaluation and legal consultation services to the organization its affiliates and subsidiaries Analyze problems and develop solutions for meeting the parent companys objectives Review draft and negotiate legal documents Analyze problems and develop solutions for meeting the parent companys objectives Advise solutions for client development strategies marketing and productivity Consult on legal and program issues to actively manage risks Improve Law Firms profitability and efficiency using legal practice knowledge Perform legal research and analysis on qualified retirement plans and securities Support clients to gather facts on resolving litigation subpoenas and complaints analyze individual disputes and conduct legal research to execute a course of action Monitor legal and regulatory developments and analyze legally with required execution
Full Time
Key Skills :
legal
research
, law, legal issues, legal documentation, legal advice...
Job Description:
Within the mission vision and values of Riyadh Cables Group of Companies provides legal advice and opinion on all legal issues especially on contrac...
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INR
Array
Array
Array-Array
"YEARLY"
Temporary C & D QA
associate
Temporary C & D QA
associate
Abbott India Ltd
2-4 Yrs
14 hrs ago
Turkey
Turkey
Not Mentioned
IN
0
Turkey
Temporary C & D QA
associate
12-12-2019
2020-03-11
QUALIFICATIONS University degree preferably in Chemistry Chemical Engineering or Pharmacy Minimum 2-4 years of experience in quality control quality assurance and warehouse operations at pharma industry Thorough knowledge and experience of cGMP quality and compliance regulations Good Warehouse Practices cGWP Good Distribution Practices cGDP Have an experience in product market release batch documentation reviews return goods customer complaints management 2D barcoding system applications Experience in QA documentation practices SOPs training change control systems exceptions and CAPA management Good knowledge of supplier evaluation and qualification process and audit management Experience in artwork development and control is a valuable asset Excellent command of English verbal and written Strong analytical thinking problem solving and negotiation skills Deliver results and excellent in follow-up A good team player with strong communication capabilities Proficient computer skills Position will be located in Gebze mraniye Maintaining quality systems to ensure compliance to company policies cGMP cGWP and local regulations Implementing quality assurance processes in affiliate and 3PL Third Party Logistics warehouse Reviewing and approving batch documentation for incoming products secondary packaging processes and product release to market return goods management Complaint management and documentation Managing related documentation systems in the affiliate and warehouse updating related procedures Reviewing and approving change controls exceptions deviations and CAPAs taking related actions to prevent the occurrence of any non-conformances relating to product process and quality systems Managing supplier qualification system for affiliate preparing annual supplier audit schedule monitoring and auditing suppliers performance monitoring for suppliers Preparing annual training and audit schedules for affiliate performing internal audits and monthly training system follow-up
Full Time
Key Skills :
suppliers, customer complaints, change control, supplier audit, capa...
Job Description:
QUALIFICATIONS University degree preferably in Chemistry Chemical Engineering or Pharmacy Minimum 2-4 years of experience in quality control qua...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Scientist
associate
Scientist
ASTRAZENECA PHARMA INDIA LTD
8-11 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
associate
Scientist
12-12-2019
2020-03-11
If youre inspired by the possibilities of science to change lives and you thrive when making brave decisions join us MedImmune is the worldwide biologics research and development arm of AstraZeneca Here youll have the opportunity to make a difference in peoples lives every day As one of the worlds premier biotechnology companies our mission is centered on delivering life-changing products that advance world health and help fight and cure disease Here at MedImmune youll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients lives Were constantly pushing the boundaries of science to deliver life-changing medicines to patients with a passion for discovery and a pipeline to show for it Were pioneering innovative research and exploring novel pathways across key therapeutic areas including oncology respiratory inflammation and autoimmunity cardiovascular and metabolic disease and infection and vaccines And were industry-leading in immunology protein engineering and translational science We offer a unique and strong collaborative network as part of the AstraZeneca family as together we explore synergies between small and large molecules MedImmune has a dynamic environment that fosters collaboration and innovation We attract top minds and we nurture and build top talent Position Summary Key Responsibilities 1 Perform cell culture maintain cell lines and perform routine lab equipment maintenance 2 Carry out bioanalytical cell-based assay testing of recombinant protein therapeutics under cGMP Make detailed observations analyze data interpret results and exercise appropriate technical discretion in the design execution and interpretation of experiments in an independent manner 3 Qualification transfer and validation of cell-based bioassays for biological characterization and testing of biopharmaceutical products 4 Assay investigations and troubleshooting 5 Prepare review technical reports SOPs and technical summaries present at internal external meetings 6 Lead investigation for non-conformances and coordinate equipment validation Requirements Qualifications
Full Time
Key Skills :
equipment maintenance, supervision, innovation, equipment validation, documentation...
Job Description:
If youre inspired by the possibilities of science to change lives and you thrive when making brave decisions join us MedImmune is the worldwide bio...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
associate
Cloud Services Engineer - Tier2
associate
Cloud Services Engineer - Tier2
Opentext Technologies India Pvt Ltd
3-4 Yrs
14 hrs ago
Hyderabad
Hyderabad
Telangana State
IN
0
Hyderabad
associate
Cloud Services Engineer - Tier2
12-12-2019
2020-03-11
OPENTEXT - THE INFORMATION COMPANY As the Information Company our mission at OpenText is to create solutions and deliver services that redefine the future of digital Be part of a winning team that leads the way in Enterprise Information Management The opportunity System Engineers are responsible for maintaining 7x24x365 uptime and availability for all IT Corporate and commercial Cloud Services The position reports directly to the Cloud Support Operations shift Manager and is responsible for second level support through troubleshooting restoring and escalations events to ensure positive health of all systems environments The Tier2 Cloud Support Operations team performs as the Point of Contact POC for all critical incident event escalations from NOC Tier1 Advanced Resolution teams and 3rd level support teams who identify potential service impacts They will be responsible for incident ticket management across multiple services environments requiring updating and resolution of service requests and incidents events while meeting response resolution OLA SLAs and MTTR goals You are great at The role requires oversight of vendor maintenance activities to ensure they are actively managed and completed as required Additionally Tier2 Cloud Support Operations will provide guidance and on-site support and backup responsibilities for Opentext core data centers The Cloud System Engineer provides 2nd level triage and troubleshooting for events escalated by the Monitoring Specialists in NOC Tier1 Tier2 works closely with various support teams including but not limited to Engineering Professional Services and Client Services providing resolution work-arounds for all systems and services globally while ensuring OLAs SLAs are adhered to Cloud System Engineers must prioritize events and escalate as required while ensuring post event follow-up The team actively participates in all incidents Major Incidents and decision-making activities as such they must have good judgment and the ability to make sound business decisions while adhering to established policies They will act as the Technical Trainer Mentor for Monitoring Specialist resources and new Cloud System Engineer personnel providing internal training sessions cross-training in their area of expertise This will also require them to work closely with the Documentation Specialist - submitting updates for Operational procedures and policies as needed The Cloud System Engineers skill set requires a strong working knowledge of all services hardware support practices remediation tools and proper trouble-shooting techniques and procedures Cloud System Engineer is chartered with meeting or exceeding agreed to system availability numbers and driving low Mean Time to Resolution MTTR times while identifying and driving continuous process improvement providing critical insight for design process improvement and moving the organization from reactive to proactive Incident avoidance This will be done through active participation in post-event follow-up discussions and contributions to Problem Management identifying gaps known errors and assisting in root cause analysis They must be capable of consulting and communicating effectively with monitoring personnel system engineers developers and system SMEs to isolate hardware or system failures and ensure the proper course of remediation Good verbal and written communication skills are required to effectively communicate and notify cross-functional Opentext departments including but not limited to Executive Management IT Operations and International Regions both Commercial and IT What it takes Liberal Arts degree two years of secondary schooling and or equivalent IT job experience and training Minimum of 3 - 4 years of relevant IT experience Proficient with Unix Linux Windows based OS Networking Cisco Ability to articulate clearly both in written and verbal communications Must be willing to work any shift in a 24x7x365 work environment weekend and Holiday hours required Preferred Qualifications Knowledge and use of common industry monitoring tools ITIL Best Practices and Methodologies certifications and or knowledge The skills needed to make determinations of prioritization on critical system issues while meeting changing or conflicting priorities while maintaining effectiveness Coordination organization and teaming skills Self-motivated and quality-driven balanced with technical analysis and support abilities Ability to multi-task and respond to priority issues effectively Ability to work independently with minimal supervision Must be accountable and responsible Seek opportunities for continued personnel and business growth and improvement At OpenText we understand and value diversity in our employees and are proud to be an Equal Opportunity Employer
Full Time
Key Skills :
mttr, supervision, documentation, process improvement, root cause analysis...
Job Description:
OPENTEXT - THE INFORMATION COMPANY As the Information Company our mission at OpenText is to create solutions and deliver services that redefine the...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
research
Scientist - Analytical - Separation Scientist
research
Scientist - Analytical - Separation Scientist
PI Industries Ltd
1-5 Yrs
14 hrs ago
Udaipur
Udaipur
Rajasthan
IN
0
Udaipur
research
Scientist - Analytical - Separation Scientist
12-12-2019
2020-03-11
Position Description Business Division CreAgro Department Chemistry Locaton Udaipur Position Title Associate Research Scientist Analytical-Separation Scientist Level E1 E4 Reporting to Title Team Leader Group Leader - Analytical Position Purpose The incumbent should be an MSc in Chemistry or Analytical Chemistry Organic Chemistry from a reputed University in India He should have at least 1-2 years of hands on experience either in a Prep HPLC or an Auto Purification System He should be well versed with reverse purification technique and a sound Knowledge of column chemistry Good understanding of theoretical principles of different chromatography techniques is a must Strategic Responsibilities Actively imbibing the values and philosophy of PI Industries Efficient contribution to the overall success of CreAgro Analytical Chemistry through scientific contribution and supporting team performance according to objectives and targets being set by the leadership team Fullfilling requirements and achieveing goals set by the Team Leader and Group Leader Analytical Chemistry Working as a team member contribute to the team objective with special focus on achieving and exceeding the set target and development of individual strengths Remain at the cutting edge of knowledge required for the new a i discovery activity in crop protection through constant updating of personal knowledge and own skill-sets Operational Responsibilities Should be conversant with principles of different analytical techniques chromatography and spectroscopy Expected to purify small molecules comprising of different chemo types positional isomers by developing suitable chromatography methods A very sound knowledge and experience in different column chemistry is essential Routine maintenance of the prep instrument Keep self updated on the state of the art In field of separation science Continuous documentation and reporting of all analytical results Need to work on an instrument other than Prep HPLC as secondary responsibility Comply to all safety requirements of the role responsible for individual safety and lab housekeeping Financial Responsibilities People Responsibilities Collaborate with team members and cross functional teams to ensure meeting research objectives Ensure smooth working by maintaining high level of morale and working ethics Ensure team harmony through collaboration and active participation in all team discussion Education Qualification MSc Organic Chemistry Analytical Chemistry from a reputed University Institute with excellent academic credentials Work Experience 1-5 years of hands on experience on Prep HPLC Auto Purification System Industry to be Hired from Agro Chemical Pharma Research Universities or Institutes Functional Competencies Scientific Knowledge Research Approach Data Analysis Experimentation Skills Interaction Complexity and Team Work Interaction Frequency Purpose of Interaction Internal Team Members Group Leader As and when required Planning work discussing results of experiments resolving doubts for hiring and HR related issues for reimbursement claims
Full Time
Key Skills :
group leader, safety, team work, documentation, planning...
Job Description:
Position Description Business Division CreAgro Department Chemistry Locaton Udaipur Position Title Associate Research Scientist Analytica...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Professional Services Consultant - EPS Packaging
Professional Services Consultant - EPS Packaging
Electronics for Imaging, Inc
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Professional Services Consultant - EPS Packaging
12-12-2019
2020-03-11
WE are Self-starters WE are Passionate WE are Relationship builders WE are Innovative We are Nimble and WE are Transparent WE are SPRINTers We believe in challenging you then providing you the room and flexibility to deliver EFI is looking for a Professional Services Consultant to join our EPS Business Unit This is a telecommute role and you must be based near a major airport A Professional Services Consultant will be responsible for providing professional services to new and existing EFI customers in the Corrugated Sub Segment of Packaging Industry Services can include implementation installation analysis documentation development and training as well as diagnosing and resolving operating system network database and other issues Services are provided both at client site and via phone email and Internet Principal Duties and Responsibilities Develop and deliver Consulting Services around the use of EFI MES Manufacturing Execution PBS Packaging Business System and supporting applications Develop and maintain standardized training documentation and supporting materials Ensure any client issues are identified quickly forwarded to the proper resources and resolved in a timely manner to ensure key project milestones are met Work with EFI clients to analyze and interpret business requirements provide customized solutions within the core product while offering industry best practices Organize and schedule client customization deliverables as required by EFI client Professional Services projects Provide ERP and industry specific knowledge transfer utilizing EFI consulting methodology and documentation Assist teammates with issues to ensure project objectives are being met Be an Ambassador of EFI Job Requirements Excellent organizational communication written and problem solving skills Excellent presentation skills Excellent customer service skills Spanish language fluency an asset Experience with Enterprise Resource Planning Management Information Systems Experience with EFI CTI MES PBS A strong technical background and solid knowledge of the following would be considered an asset SQL Server Structured Query Language SQL VPNs Citrix and Terminal Services IIS Crystal Reports Microsoft Windows Networking Must be able to manage multiple priorities Working knowledge of Client Server architecture Packaging industry experience specializing in corrugate segment Travel Requirements Travel expectation is up to 75 percent Education Bachelors degree in Computer Science Printing or equivalent experience Experience Four or more years experience providing professional services and or equivalent ERP implementation experience We move quickly with the purposeful intention of solving a problem accomplishing a goal and ultimately making a difference for our customers partners colleagues and shareholders EFI SPRINTers take action and adapt to changes in order to transform our customers businesses to be more productive and profitable through innovation in a digital print business EFI is an Affirmative Action EEO Protected Veteran Disabled Employer LI-RJ1
Full Time
Key Skills :
manufacturing, action, mes, innovation, implementation...
Job Description:
WE are Self-starters WE are Passionate WE are Relationship builders WE are Innovative We are Nimble and WE are Transparent WE are SPRINTers We b...
Apply Now
INR
Array
Array
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"YEARLY"
Shipping
associate
I
Shipping
associate
I
Emerson
0-1 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Shipping
associate
I
12-12-2019
2020-03-11
Shipping Associate I Requisition ID 19012597 Primary Location United States-Texas-Stafford Job Function Manufacturing Operations Responsibilities Maintain the CDP Customer delivery Performance metric daily by revising OPD per the rules and tracking all documentation Manage the RTV Return to Vendor process from Packing to Shipping Manage the Special Paint Process from Packing to Shipping Maintain Trade Compliance records including AES filings with freight forwarders Manage the Parts and Valves staging racks daily Assist in shipping orders for outside machining Work with the Packers for getting orders packed on time Requirements Applies attention to detail and task accuracy Physical tasks include walking grasping carrying lifting seeing hand-eye coordination listening writing and speaking Mental tasks include reading interpreting calculating measuring and communicating Ability to successfully complete various in-house and customer safety training programs QUALIFICATIONS High School Diploma G E D or equivalent education 0-1 years of experience Must be very punctual Must have a strong work ethic Must be able to work with little or no supervision Prefer someone with prior logistics experience Expertise with SAP is mandatory Work Authorization No calls or agencies please Emerson will only employ those who are legally authorized to work in the United States This is not a position for which sponsorship will be provided Individuals with temporary visas such as E F-1 H-1 H-2 L B J or TN or who need sponsorship for work authorization now or in the future are not eligible for hire Equal Opportunity Employer Emerson is an Equal Opportunity Affirmative Action employer All qualified applicants will receive consideration for employment without regard to sex race color religion national origin age marital status political affiliation sexual orientation gender identity genetic information disability or protected veteran status We are committed to providing a workplace free of any discrimination or harassment If you have a disability and are having difficulty accessing or using this website to apply for a position you can request help by calling 1-314-553-2544 V TTY TDD or by sending an email to idisability administrator emerson com About Emerson Imagine being surrounded by intelligent driven and passionate innovators all working toward the same goalto create groundbreaking solutions that leave our world in a better place than we found it Emerson is a global technology and engineering company providing innovative solutions for customers in industrial commercial and residential markets Our Emerson Automation Solutions business helps process hybrid and discrete manufacturers maximize production protect personnel and the environment while optimizing their energy and operating costs Our Emerson Commercial and Residential Solutions business helps ensure human comfort and health protect food quality and safety advance energy efficiency and create sustainable infrastructure A dynamic environment is what youll discover at Emerson a Fortune 500 company with 14 5 billion in sales and 155 manufacturing locations worldwide Together were changing the world and we have all the resources to help you achieve your professional goals Whether youre an established professional looking for a career change an undergraduate student exploring options or recently received your MBA degree youll find a variety of opportunities at Emerson Join our team and start your journey today
Full Time
Key Skills :
production, lifting, safety, supervision, manufacturing...
Job Description:
Shipping Associate I Requisition ID 19012597 Primary Location United States-Texas-Stafford Job Function Manufacturing Operations Respo...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Clinical
research
Quality Manager
Clinical
research
Quality Manager
ASTRAZENECA PHARMA INDIA LTD
5-8 Yrs
14 hrs ago
Turkey
Turkey
Not Mentioned
IN
0
Turkey
Clinical
research
Quality Manager
12-12-2019
2020-03-11
Background Qualifications University degree preferably from Healthcare related areas Pharmacy Veterinary Chemistry Biology Medical etc Faculties Advanced level of English Minimum 5 year experiences in Clinical Research preferably 3 years in Project Management and at least 1 year in Clinical Research quality positions Project management skills Strong communication and negotiation skills Ability to prioritize and handle multiple tasks Basic coaching skills and good at team work Financial management skills Effective planning and organizational skills with result-oriented approach Stakeholder management experience Analytical thinking critical reasoning ability Good command of MS Office applications No restriction to travel Driving License No military obligation for male candidates Summary Leading the local study teams consisting of monitors and study administrators at country level to deliver committed components of clinical studies according to agreed resources budget and timelines Ensuring that study sites are identified site qualifications performed set up initiated monitored closed and documentation archived Ensuring timely submissions of proper application documents to Ethic Committee Regulatory Authority Close communication with global study teams and overall responsibility for study commitments for timely delivery of data to required quality as agreed with global Creating and implementing alternative action plans proactively in order to reach the targeted patient numbers monitoring the patience admission processes in coordination with the researchers planning and taking the necessary precaution when required Ensuring the compliance of the clinical research process with ICH-GCP practices the study protocol AZ Global and Local Clinical SOPs and the Ministry of Health Clinical Research Regulations being knowledgeable about these procedures and keeping abreast of any changes and revision Participating in system process improvement projects within global and local task groups consisting of employees from different units
Full Time
Key Skills :
sop, action, team work, documentation, process improvement...
Job Description:
Background Qualifications University degree preferably from Healthcare related areas Pharmacy Veterinary Chemistry Biology Medical etc Facu...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Customer Service
associate
Customer Service
associate
Emerson Electric Co India Pvt Ltd
0-3 Yrs
14 hrs ago
Canada
Canada
Not Mentioned
IN
0
Canada
Customer Service
associate
12-12-2019
2020-03-11
The Customer Service Associate is responsible for coordinating with customers suppliers local business partners and internal teams to successfully deliver on customer valve needs Associates are also responsible for ensuring customer satisfaction and on-time and on-budget delivery Management of projects with a focus on cost accountability and profit is key Major Areas of Accountability Provide quotations Gather cost information Determine delivery timelines Identify and communicate potential constraints or special considerations Create orders Review and confirm purchase order information Enter orders in Oracle Issue vendor purchase orders work orders and design drawings to machine shop Prepare and file order information including ensuring valve documentation is maintained and updated Invoice completed orders Manage orders Audit active order status Update customers and management on order status Follow-up on active orders to resolve any issues and assess impacts on delivery Communicate with Engineering to resolve any manufacturing issues or determining alternate solutions Arrange for any special requirements such as customs transportation special testing or shipping specifications Train other customer service associates Other functions as assigned and necessary Qualifications Required Post-secondary degree certification or equivalent experience Strong communication skills verbal and written Proven ability to be agile and deliver results under constrained timelines including the ability to manage multiple priorities at once project management experience is an asset Excellent analytical and problem solving skills with the ability to think critically Microsoft office expertise Word Excel basic computer skills Preferred Prior experience in business-to-business customer service or in a manufacturing industrial environment Experience with valves instrumentation Familiarity with machining or reading machine drawings Experience with Oracle or similar business systems Purchasing Supply-Chain experience About Emerson At Emerson we are innovators and problem-solvers focused on a common purpose leaving our world in a better place than we found it Each and every day our foundational valuesintegrity safety and quality supporting our people customer focus continuous improvement collaboration and innovationinform every decision we make and empower our employees to keep reaching higher As a global technology and engineering leader we provide groundbreaking solutions for customers in industrial commercial and residential markets Our Automation Solutions business helps process hybrid and discrete manufacturers maximize production and protect personnel and the environment while optimizing their energy and operating costs Our Commercial Residential Solutions business helps ensure human comfort and health protect food quality and safety advance energy efficiency and create sustainable infrastructure Emerson a Fortune 500 company with 17 4 billion in sales more than 20 Innovation Solutions Engineering Centers and 200 manufacturing locations worldwide is committed to helping employees grow and thrive throughout their careers Whether youre an established professional looking for a career change an undergraduate student exploring options or a recent MBA graduate youll find a variety of opportunities at Emerson Join our team and start your journey today
Full Time
Key Skills :
production, safety, manufacturing, instrumentation, innovation...
Job Description:
The Customer Service Associate is responsible for coordinating with customers suppliers local business partners and internal teams to successfully d...
Apply Now
INR
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Array
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"YEARLY"
Production Sanitization
associate
-GMP
Production Sanitization
associate
-GMP
Avantor
1-4 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Production Sanitization
associate
-GMP
12-12-2019
2020-03-11
Job SummaryThe Production Sanitization Associate is responsible for carrying out routine tasks at a customer site including but not limited to operating and maintaining washers and cleaning of industrial grade soiled equipment Must be cognizant of and adhere to Standard Operating Procedures Work Instructions Job Break-down Sheets and GMP regulatory requirements in a FDA regulated production environment MAJOR JOB DUTIES AND RESPONSIBILITIES List in order of importance Operate and maintain washers and equipment including documentation in customers computerized maintenance management systems Ensure parts are available when needed and that there are no interruptions to the manufacturing schedule Replenish and maintain washer chemical supplies in multiple locations Inactivation of equipment containing product via chemical means Collect soiled equipment and separate into correct production streams Disassemble equipment following proper procedure Operate and maintain lifts and hoists Empty and clean drums and transport bins Clean and inspect dollies Stock sort collect and transport gowns and supplies Maintain and adhere to strict training requirements Remove trash as needed Maintain 6 work areas in a GMP 6S and an inspection ready state at all times Performs other duties as assigned QUALIFICATIONS Education Training Experience and Certifications High school diploma or GED required 1 years of applicable job experience 1 years of wash experience in a GMP environment preferred Knowledge of and ability to use multiple computer programs KNOWLEDGE SKILLS AND ABILITIES Those necessary to perform the job competently Conform to all customer requirements for background checks health and safety issues and security clearances Must be able to lift 50 pounds Strong communication skills Excellent customer service skills display a professional can-do attitude Perform duties with the highest regard for safety and quality Must be flexible motivated and have the ability to act independently Must exhibit core values and behaviors Integrity respect collaboration accountability etc Must have ability to understand read and write technical information ENVIRONMENTAL WORKING CONDITIONS PHYSICAL EFFORT Under Typical Positions The work environment characteristics and physical effort described here are representative of those an associate encounters while performing the essential functions of this job Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions Primarily works in a double-gowned GMP manufacturing environment with adequate lighting and ventilation and a normal range of temperature and noise level Work assignments are diversified Examples of past precedent are used to resolve work problems New alternatives may be developed to resolve problems A frequent volume of work and deadlines impose strain on a routine basis Physical effort is required Does require walking standing bending reaching lifting or carrying objects that may weigh up to 50lbs The above statements are intended to describe the general nature and level of work being performed by people assigned to this job They are not intended to be an exhaustive list of all responsibilities skills efforts or working conditions associated with a job DISCLAIMER The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification They are not intended to be construed as an exhaustive list of all responsibilities duties and skills required of employees assigned to this position Avantor is proud to be an equal opportunity employer EEO Statement We are an Equal Employment Affirmative Action employer We do not discriminate in hiring on the basis of sex gender identity sexual orientation race color religious creed national origin physical or mental disability protected Veteran status or any other characteristic protected by federal state province or local law If you need a reasonable accommodation for any part of the employment process please contact us by email at TalentManagement vwr com and let us know the nature of your request and your contact information Requests for accommodation will be considered on a case-by-case basis Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address For more information about our commitment to equal employment opportunity please Privacy Policy Links to 1 EEO is the Law poster and any supplements 2 pay transparency nondiscrimination statement and 3 if desired Company EEO AA Statement
Full Time
Key Skills :
production, documentation, safety, lifting, maintenance management...
Job Description:
Job SummaryThe Production Sanitization Associate is responsible for carrying out routine tasks at a customer site including but not limited to operat...
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INR
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"YEARLY"
associate
/ Sr.
associate
- Electrical Maintenance
associate
/ Sr.
associate
- Electrical Maintenance
CANVAS27.com
1-6 Yrs
14 hrs ago
Ahmedabad, Bangalore, Chennai, Delhi, Ncr...
Ahmedabad
,
Gujarat
IN
0
Ahmedabad
Bangalore
,
Karnataka
IN
0
Bangalore
Chennai
,
Tamil Nadu
IN
0
Chennai
Delhi
,
Delhi
IN
0
Delhi
Ncr
,
Not Mentioned
IN
0
Ncr
Gurgaon
Haryana
IN
0
Gurgaon
associate
/ Sr.
associate
- Electrical Maintenance
12-12-2019
2020-03-11
Experience in Handling operation and maintenance of electrical in Pharma- Drug product DP Injectable formulation Pre-filled Syringe Cartridge filling and Vial filling Drug substance DS Fermentation Microbial Mammalian manufacturing Should have experience in Black utility operation Chiller IBR boiler Cooling towers Air compressors Diesel generator transformer LT HT panel operation UPS maintenance fire hydrant system ETP STP FO yard Documentation activity related to electrical Knowledge on Preventive maintenance and breakdown maintenance If the above job does not suit your profile you can still apply as we have various vacancies across different cities job areas For details of other jobs you can also email us else check our website Thanks Hiring Team Canvas27 com
Full Time
Key Skills :
electrical maintenance, boiler, breakdown maintenance, preventive maintenance, ups...
Job Description:
Experience in Handling operation and maintenance of electrical in Pharma- Drug product DP Injectable formulation Pre-filled Syringe Cartridge fill...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Finance Officer
Finance Officer
JECRC University
15-20 Yrs
13 hrs ago
Jaipur
Jaipur
Rajasthan
IN
0
Jaipur
Finance Officer
12-12-2019
2020-03-11
Desirable requirements Essential Requirements A Masters degree with at least 55 marks or its equivalent B grade in UGC seven-point scale 15 years of appropriate experience of financial management of which 8 years as Deputy Registrar Deputy Finance Officer or an equivalent post of a University affiliated college public sector undertaking autonomous organization multinational organization Government OR Comparable experience in a research establishment and or other institutions of higher education OR With an overall service of 15 years as Deputy Finance Officer including 8 years in post of Assistant Registrar Assistant Finance Officer
Full Time
Key Skills :
finance,
research
, education, management, financialmanagement...
Job Description:
Desirable requirements Essential Requirements A Masters degree with at least 55 marks or its equivalent B grade in UGC seven-point scale 15 ye...
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INR
Array
Array
Array-Array
"YEARLY"
associate
Director of Sales Marketing
associate
Director of Sales Marketing
Hyatt
2-3 Yrs
13 hrs ago
Hyderabad
Hyderabad
Telangana State
IN
0
Hyderabad
associate
Director of Sales Marketing
12-12-2019
2020-03-11
You will be responsible to provide an excellent and consistent level of administrative support to your department Ideally with a relevant degree or diploma in Hospitality or Tourism management Minimum 2 years work experience in hotel operations Good customer service communications and interpersonal skills are a must
Full Time
Key Skills :
finance, customerrelations, customerservice, interpersonalskills, interpersonalskills...
Job Description:
You will be responsible to provide an excellent and consistent level of administrative support to your department Ideally with a relevant degree ...
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INR
Array
Array
Array-Array
"YEARLY"
Female Anchor
Female Anchor
Leading Company
2-7 Yrs
13 hrs ago
Chandigarh
Chandigarh
Chandigarh
IN
0
Chandigarh
Female Anchor
12-12-2019
2020-03-11
Research local community state national and international current events Meet with the news director reporters and other news anchors to be briefed on the days news Collaborate with the news director to choose stories to broadcast considering audience preferences Organize the news to present the most interesting pieces first Revise scripts and prepare to deliver them on-air Ensure late-breaking news is added to newscasts Engage in commentary Interview guests and other members involved in particular stories Introduce news correspondents reporting on scene and ask them relevant questions Comply with the moral code of the journalistic profession Keep abreast of news developments by studying papers attending events etc Stay in contact with industry professionals Skills Proven work experience as a news anchor Understanding of the newscast process Broad knowledge of local national and international affairs e g political economic legislative and cultural
Full Time
Key Skills :
emale anchor,
research
local community...
Job Description:
Research local community state national and international current events Meet with the news director reporters and other news anchors to be briefed...
Apply Now
INR
Array
Array
Array-Array
"YEARLY"
Product Manager
Product Manager
V- Konnect Associates
5-10 Yrs
13 hrs ago
Mumbai City
Mumbai City
Not Mentioned
IN
0
Mumbai City
Product Manager
12-12-2019
2020-03-11
1 Create product concept presentations formally present to executive ownership level 2 Review documentation and launch articles Setting training modules 3 Determines customers needs and desires by specifying the research needed to obtain market information 4 Assesses market competition by comparing the companys product to competitors products 5 Obtains product market share by working with sales director to develop product sales strategies 6 Provides information for management by preparing short-term and long-term product sales forecasts and special reports and analyses answering questions and requests 7 Responsible for new product development from formulation to launch includes ingredient compatibility 8 Participate in meetings with the Research and Development Department on new product development and provide technical input on new product design and concepts 9 Assess and vet new product opportunities to determine viability dosage regulatory compliance and scientific validation 10 Analyze and evaluate clinical and laboratory research as it applies to the formulation and delivery of new and existing products 11 Complete competitive analysis and pricing 12 Manage product launch and follow through to ensure meeting deadlines 13 Write technical and marketing support documents as appropriate 14 Review internal documents for consistency and accuracy ads articles all marketing pieces product directory etc as appropriate 15 Research and respond to elevated member issues involving product and ingredient
Full Time
Key Skills :
product development, product management, , delivery, new product design...
Job Description:
1 Create product concept presentations formally present to executive ownership level 2 Review documentation and launch articles Setting training m...
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INR
Array
Array
Array-Array
"YEARLY"
associate
Scientist
research
and Development
associate
Scientist
research
and Development
Abbott India Ltd
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
associate
Scientist
research
and Development
12-12-2019
2020-03-11
Abbott is a global healthcare leader that helps people live more fully at all stages of life Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medical devices nutritionals and branded generic medicines Our 103 000 colleagues serve people in more than 160 countries We are seeking an Associate Scientist Research and Development Job Summary o Leads projects Provides technical review direction and feedback to others o Conducts research Main Responsibilities o Assay Development Design Control core team member responsible for Design Control activities which may include design inputs design planning design change requests deliverables design reviews Works with new systems such as APLM and SBM O Experimental procedures Conducts experiments accomplishes established milestones and summarizes data o Recommends options for other experiments o Presents data within team o Expertise and Problem Solving Troubleshoots instrumentation or experiments recognizes and assists with technical problems o Anticipates recognizes and resolves technical problems o Project Planning Participates in planning project tasks providing input to accomplish assigned tasks o Implements project plans comprehending resource budget facility and regulatory requirements o Lab Safety Participates in routine maintenance and lab safety o Documentation Appropriately documents experimental procedures and results according to established guidelines o Appropriately documents design control activities according to established guidelines o Quality Responsible for implementing and maintaining the effectiveness of the quality system o Translates top-level goals to specific project level goals for individual team member o Establishes and reviews complex plans for multiple projects or activities o Plans resource allocation and distribution o Responsible for CAPA activities CAPA activities include nonconformances potential nonconformances and investigations Accountability Scope o Works across functional areas programs within division o Contributes to the definition and timely achievement of goals o Responsible for project completion Minimum Qualifications B S M S in life of physical science Preferred Qualifications Basic Computer Skills Knowledge of analytical instruments assigned by supervisor
Full Time
Key Skills :
safety, instrumentation, documentation, problem solving, planning...
Job Description:
Abbott is a global healthcare leader that helps people live more fully at all stages of life Our portfolio of life-changing technologies spans the sp...
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INR
Array
Array
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"YEARLY"
Sr.
associate
, Quality Assurance
Sr.
associate
, Quality Assurance
Exela Technologies
1-6 Yrs
14 hrs ago
Chennai
Chennai
Tamil Nadu
IN
0
Chennai
Sr.
associate
, Quality Assurance
12-12-2019
2020-03-11
Sr Associate Quality Assurance 1 to 2 Years Chennai Dowlath Position Type Fulltime Requisition ID 5640 Level of Education 3 Year Degree or equivalent Years of Experience 1 to 2 Years Job Summary Responsible for the implementation and management of the Quality Control Program which includes the coordination performance and execution of inspections checks tests and sampling procedures of records The Quality Control Auditor is responsible for assuring that the quality of the work meets or exceeds the corporation contractual requirements and maintains the standard of excellence established Essential Functions and Responsibilities 1 Performs verification on incoming in-process and outgoing records 2 Performs tests and hands-on inspections during and after production to ascertain that records are fee from flaws and are of the highest quality 3 Compares paper to electronic images using a statistically valid sampling method 4 Maintains record of inspections analyzes test results and prepares statistical reports for review 5 Reports quality problems or findings to supervisor and follow-up to ensure that correction action will take place 6 When quality standards are not met will instruct workers on how to address the issues or recommend different production techniques to supervisor 7 Interacts with other departments to ensure compliance with specification and to facilitate the acceptance of performance 8 Complies with legal requirements and industry standards and maintains accurate documentation as an important function of the quality control team 9 Supervision enforcement and updating of the corporations quality control manual Key Skills Persuasive communication skills necessary to collect essential information answer questions and direct callers to appropriate personnel in a professional and courteous manner Developed interpersonal skills necessary to establish and maintain effective working relationships with co-workers other business areas and government agencies as required Planning and organizational skills necessary to coordinate workload around complex multiple assignments Intermediate knowledge of computerized applications for example word processing spreadsheet database and presentation Minimum Qualifications Bachelors degree highly preferred 3 years experience in related role Additional Desired Qualifications None Physical Requirements Physical demands with activity or condition requiring a considerable amount of time include sitting and typing keyboarding using a computer i e keyboard mouse and monitor or adding machine Physical demands may include walking carrying reaching standing and stooping May require occasional lifting lowering pushing or pulling up to 25 lbs Healthcare knowledge Basic Communication skills Typing skills Disclaimer
Full Time
Key Skills :
production, lifting, supervision, action, implementation...
Job Description:
Sr Associate Quality Assurance 1 to 2 Years Chennai Dowlath Position Type Fulltime Requisition ID 5640 Level of Education 3 Year Degree o...
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INR
Array
Array
Array-Array
"YEARLY"
Production Sanitation
associate
Production Sanitation
associate
Avantor
1-4 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Production Sanitation
associate
12-12-2019
2020-03-11
Job SummaryThe Production Sanitization Associate is responsible for carrying out routine tasks at a customer site including but not limited to operating and maintaining washers and cleaning of industrial grade soiled equipment Must be cognizant of and adhere to Standard Operating Procedures Work Instructions Job Break-down Sheets and GMP regulatory requirements in a FDA regulated production environment Job Responsibilities Operate and maintain washers and equipment including documentation in customer s computerized maintenance management systems Ensure parts are available when needed and that there are no interruptions to the manufacturing schedule Replenish and maintain washer chemical supplies in multiple locations Inactivation of equipment containing product via chemical means Collect soiled equipment and separate into correct production streams Disassemble equipment following proper procedure Operate and maintain lifts and hoists Empty and clean drums and transport bins Clean and inspect dollies Stock sort collect and transport gowns and supplies Maintain and adhere to strict training requirements Remove trash as needed Maintain 6 work areas in a GMP 6S and an inspection ready state at all times Performs other duties as assigned Experience Skills Conform to all customer requirements for background checks health and safety issues and security clearances Must be able to lift 50 pounds Strong communication skills Excellent customer service skills display a professional can-do attitude Perform duties with the highest regard for safety and quality Must be flexible motivated and have the ability to act independently Must exhibit core values and behaviors Integrity respect collaboration accountability etc Must have ability to understand read and write technical information Qualifications High school diploma or GED required 1 years of applicable job experience 1 years of wash experience in a GMP environment preferred Knowledge of and ability to use multiple computer programs Environmental Working Conditions Physical Effort The work environment characteristics and physical effort described here are representative of those an associate encounters while performing the essential functions of this job Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions Primarily works in a double-gowned GMP manufacturing environment with adequate lighting and ventilation and a normal range of temperature and noise level Work assignments are diversified Examples of past precedent are used to resolve work problems New alternatives may be developed to resolve problems A frequent volume of work and deadlines impose strain on a routine basis Physical effort is required Work but does require walking standing bending reaching lifting or carrying objects that may weigh up to 50lbs DISCLAIMER The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification They are not intended to be construed as an exhaustive list of all responsibilities duties and skills required of employees assigned to this position Avantor is proud to be an equal opportunity employer
Full Time
Key Skills :
production, documentation, safety, lifting, maintenance management...
Job Description:
Job SummaryThe Production Sanitization Associate is responsible for carrying out routine tasks at a customer site including but not limited to operat...
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INR
Array
Array
Array-Array
"YEARLY"
Sales
associate
Sales
associate
Freelancer Akshay Reddy Hiring For SHIPPING
6-11 Yrs
13 hrs ago
Chennai
Chennai
Tamil Nadu
IN
0
Chennai
Sales
associate
12-12-2019
2020-03-11
Sales Associate is responsible for dealing with any and all customer questions about the products and services the company offers A Sales Associate is expected to be continuously updating their knowledge of the company products services and policies Complaint handling is a critical part of this position Turning a frustrated customer into a happy customer while adhering to company policies requires a combination of empathy and tact Another key responsibility is maintaining the presentation of the sales floor products signage and displays Sales Associate Responsibilities Greeting customers responding to questions improving engagement with merchandise and providing outstanding customer service Operating cash registers managing financial transactions and balancing drawers Achieving established goals Directing customers to merchandise within the store Increasing in store sales Superior product knowledge Maintaining an orderly appearance throughout the sales floor Introducing promotions and opportunities to customers Cross-selling products to increase purchase amounts Sales Associate Requirements An Associates degree or high school diploma Retail sales experience A professional appearance Maintain a positive attitude and focus on customer satisfaction in a fast-paced environment The ability to read write and perform basic math The ability to stand and walk for extended periods of time
Full Time
Key Skills :
internationalmoves, sales, driverretention, passenger, ltlshipping...
Job Description:
Sales Associate is responsible for dealing with any and all customer questions about the products and services the company offers A Sales Associate i...
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INR
Array
Array
Array-Array
"YEARLY"
Optical Lab Shipping
associate
3rd shift Sun-Thu 1...
Optical Lab Shipping
associate
3rd shift Sun-Thu 1...
WALMART INDIA
0-3 Yrs
14 hrs ago
United States Of America, Usa
United States Of America
,
Not Mentioned
IN
0
United States Of America
Usa
Not Mentioned
IN
0
Usa
Optical Lab Shipping
associate
3rd shift Sun-Thu 1...
12-12-2019
2020-03-11