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.
Vacancy Details
Experience:
- 2-15 years in Pharmaceutical Industry, predominantly in Global Regulatory Affairs function
- Experienced in authoring and review of high-quality regulatory submissions for new & post-approval supplements / variations) in global markets (US, EU, Canada, AnZ & RoW) for Sterile Injectables, Oral Solid Dosages (OSDs) and other dosage forms.
Preferred Qualification:
- Minimum Postgraduate in Pharmacy / Life Sciences
- Suitable candidates will be contacted by our People Experience team for a virtual 1:1 interview.
Work location:
Chennai, Ahmedabad,
Mumbai & Vishakhapatnam
Interested candidates can share their resumes with IndiaTalentAcquisition@pfizer.com
