Pfizer Limited was listed on the Indian stock exchange in 1966. Today, the company has over one lac shareholders in India. With annual sales of over Rs. 2,000 crores, it is the fourth largest multinational pharmaceutical company in India. The Company has a portfolio of over 150 products across 15 therapeutic areas. Its top brands include Prevenar 13, Lyrica, Corex – DX, Dolonex, Enbrel, Becosules, Gelusil and Folvite among others. In addition to its commercial operations, Pfizer Limited also operates a state-of-the-art, award-winning manufacturing facility in Goa that produces more than a billion tablets annually.
Job Description
- Department:- Regulatory Affairs
- Experience: 02 to 15 years
- Work Location: Ahmedabad, Chennai & Vizag
Walk-In Interview Details:
- Date: 28th October 2023
- Venue: Pfizer Healthcare India Pvt. Ltd. Emerald Building, 237, Anna Salai, Chennai – 600006
- Time: 9:00 am to 6:00 pm (IST)
Preferred Experience:
- 2-15 Years in Pharmaceutical industry with major experience in Global Regulatory Affairs function.
- Authoring and/or contributing line to CMC content for DMFs/ INDs/ IMPDs/ NDAs/ BLAs/ ANDAs/ MAAs/ Post-approval variations/ Supplements and Medical Device Design History File/ Technical File/ Design Dossiser for Global markets.
- Candidates with relevant technical experience in Pharma R&D, Tech Transfer, Quality & Manufacturing, aspiring for Regulatory role can also apply, and will be considered based on merit and potential.
Interested applicants may send resumes to indiatalentacquisition@pfizer.com with the job title ‘Global Regulatory Sciences ‘ in the subject line.
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