Pfizer invites applications for Regulatory Affairs Professionals in CMC initial registrations and Life-Cycle Management roles responsible for the development of post-approval regulatory strategies and CMC authoring of supplements/ Variations/ Annual reports/ license renewals for submission to Global Health Authorities (EU, US, Canada, ANZ and RoW).
Qualification: Master’s degree in Pharmacy/ Biotechnology/ Science/ Ph.D.
Work Experience: Candidates with 2-15 years to experience in handling regulatory submissions and CMC compliance activities for Biologics and/or Small Molecules in Global Markets (US, Europe, Canada, ANZ, and RoW).
- Excellent in English communication
- Good interpersonal skills
- Attention to details
- Good project management
- Problem-solving skills
Work Location: Chennai, India
Please send your CV to email@example.com with the job title “Drug Regulatory Affairs” in the subject line.