Pfizer healthcare India pvt ltd hiring for Drug Regulatory Affairs vacancies in Chennai location
Inviting Applications for Regulatory Affairs Professionals in CMC initial registrations and Life-Cycle Management roles responsible for development of post approval regulatory strategies & CMC authoring of supplements/Variations/Annual Reports/license renewals for submission to Global Health Authorities (US, EU, CANADA, ANZ & ROW).
Qualification: Master’s Degree in Pharmacy / Biotechnology /Science / Ph. D.
Work Experience: Candidates with 2 to 15 years
Job Description :-
experience in handling regulatory submissions and CMC compliance activities for Biologics and/or Small Molecules in Global Markets (US, Europe, Canada, ANZ, & ROW).
- Excellent in English communication
- good interpersonal skills
- strong desire to work in a collaborative environment
- good analytical reasoning skills
- Attention to details
- good project management and problem solving skills.
work Location: Chennai
Please send your CV to firstname.lastname@example.org with job title as “Drug Regulatory Affairs” in Subject line.
Company website – pfizercareers.com