Sun Pharma is India’s No. 1 pharmaceutical company and a leading global player in specialty medicines. With over 40 manufacturing facilities and a diverse portfolio, we deliver high-quality medicines across 100 countries. Driven by a commitment to innovation, we continuously strive to enhance access to medicines and improve patient care, creating better health outcomes for millions around the world.
Post : Executive - Regulatory Affairs
Job Description
• To review and maintain GMP documents.
• To co-ordinate QMS related activities like Change Control etc.
• Approval of documents like SOP’s, STP’s etc.
• To Review, follow up and compilation of data for submission of USDMF, CEP, DCP, CP, MRP for New DMF submission and DMF-Amendment / Update based on the Planning to Corporate RA, Mumbai.
• To Review, follow up and compilation of data for submission of USDMF, DMF-Amendment / Update based on the Planning to Corporate RA, Gurgaon.
• To Review, follow up and compilation of data for submission of Japan, China, TGA, Canadian... for New DMF submission and DMF-Amendment / Update based on the Planning to Corporate RA, Mumbai. Compilation of raw data for Registration /re-registration and queries received from authorities for ROW market, such as China, Korea, Taiwan, Indonesia, South Africa...etc.
• To co-ordinate and organization of plant regulatory team for planning and execution of work based on the time line
Additional Information
Experience : 4-6 years
Qualification : M.Pharm, MSc
Location : Panoli, Gujarat
Job Grade : G12A Executive
Industry Type : Pharma / Healthcare / Clinical research
Business Unit : R&D1 Regulatory Affairs
End Date : 30th September 2026
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