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Glenmark Pharmaceuticals opportunities details February 2021


QUALIFICATION :- M. Pharm/B.Pharm

WORK EXPERIENCE 02 to 03 years

Officer – Regulatory Affairs

Roles & Responsibilities Compilation of ANDA dossier in eCTD format. Review of Technical data required for ANDA compilation and submission Thorough DMF review IIG Assessment of assigned products • Drafting of Controlled correspondence to the USFDA. Support different stake holders for OSD and Oral liquid dosage forms by providing regulatory strategies.

Interested candidate can share their resume at Simran.Gill@glenmarkpharma.com

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