Corporate Affairs Jobs In Mumbai

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We have been retained by a fast growing Chemical company to select a person as a Head corporate affairs/ corporate Communications.\n\nThe position is based at Mumbai.\n\nThe overall job responsibilities will include:\n\n- Developing a Strategic Inte...

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Candidates from Engineering background would be preferred. Market scenario and understanding and awareness of current trends in govement and business.\n\nExcellent academic pedigree : \n\n- Engineering Graduates (B.E./B. Tech.) from a premium techn...

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The job is responsible for management of specific Regulatory affairs work for our client / s relevant to their products in India as well as delivering the inteal Magna-Opus expectations. ...

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Prepare the checklist for documentation as per the drug and current regulatory requirements. Compilation and review of USDMF amendments\n Preparation and review of Open parts and Technical packages of API for customers ...

Corporate Affairs Openings In Mumbai

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Head Regulatory affairs function and ensure product related regulatory strategies are developed & implemented in accordance with inteational regulations, product development & commercialization strategies with minimal queries....

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preparation of registration dossier in CTD, ATD and country specific guidelines., Application compilation for local and central licensing authorities eg FDA state and CDSCO- mfg License, COPP, FSC, sound technical knowledge. Should be flexible.

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Candidate will be responsible for Ensuring preparing & submission of Dossiers for Product registration. Ensure accuracy, completeness and quality of regulatory submissions. Ensure that all product artwork is updated when necessary and submitted i...

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Preparation of regulatory affairs dossiers for registration of formulations in ROW Market specifically CIS, Anglo Africa & SEA countries as per country specific guidelines.\nRespond within timelines any query raised by registration authorities....

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To prepare the Registration and Renewal dossiers for allotted countries.\nCo-ordination with factory personnel for arrangement of Certificate Of Analysis.\nArrangement of samples ...

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1) Should be well versed with the guidelines of ICH and other regulatory.\n2) Should be well versed with the preparation of documents for license application.\n3) Should be well versed with the preparation of documents for COPP, FSC and other legal...

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Mainly South Africa Registrations
Responsible for achieving all regulatory registrations/ permissions/ renewals for pharmaceutical formulations in South Africa.
Preparing / compiling reviewing & processing dossiers for regulatory submissions in SA...

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Exclusively for South Africa Markets
Responsible for achieving all regulatory registrations/ permissions/ renewals for pharmaceutical formulations in South African markets.
Preparing / compiling reviewing & processing regulatory submissions....

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Regulatory affairsprofileDesignation:-
Officer/Executive (Can give a higher designation to a senior person)Ø Gender: MaleØ Job Location:(Mumbai)Ø Salary Range: Rs. 15,000 to 25,000 per monthØ Notice Period: Immediate ...

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2-4 yrs of experience in regulatory affairs in EU market\nExperience in Filling Annual Reports\nexperience in filling dossiers\nfilling on eCTD format\nexperience in pharma formulation company ...

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Description :

Provide direction to R&D for regulatory & drugs registration requirements for SOUTH AFRICA.
Regular interaction wit...

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Regulatory affairs -Pharmaceutical Formulations Central America Please send CV by email to careers.india@prpharma.com All applications and queries must be sent by email only to careers.india@prpharma.com...

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Preparation of registration documents, ACTD and dossiers as per country specific guidelines to support the registration of Pharmaceutical products in African, SEA, GCC, CIS and LATAM markets.*Reviewing of labeling, product monographs, artworks.

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Exclusively for South Africa Markets
Responsible for achieving all regulatory registrations/ permissions/ renewals for pharmaceutical formulations in South African markets.
Preparing / compiling reviewing & processing regulatory submissions....

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Independently handling registrations & renewals for all manufactured pharmaceutical drug products preferably veterinary.
Registrations & renewals for exports to neighbouring countries.
Preparation of documents & submission to regulatory authorities...

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Preparation of regulatory affairs dossiers for registration of formulations in ROW Market specifically CIS, Anglo Africa & SEA countries as per country specific guidelines.\nRespond within timelines any query raised by registration authorities....

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Corporate Affairs jobs in Mumbai and it's Related skills

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