Pfizer | Drug Regulatory Affairs | M.Pharma

Pfizer vacancy

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).

Required Skills: 

  • 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 with the job title “Drug Regulatory Affairs” in the subject line.



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