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
