Founded in 1849, Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.
Post : Drug Regulatory Affairs
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 of experience in handling regulatory submissions and CMC compliance activities for Biologies and/or Small Molecules in Global Markets (US, Europe, Canada. ANZ. & RoW).
Required Skills : 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
Send your CV to email@example.com with Job title as “Drug Regulatory Affairs" In Subject line
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