Job Title

USV,a top-15 pharmaceutical and biotechnology company in India, excels in the diabetes and cardio sectors and has presence in over 65 countries and is a leading producer of Metformin in India. We specialize in niche product areas across international markets, including Oral Solid Dosages (OSD), sterile products, peptides, biologics, and oncology. USV’s Biologics function is fully integrated to develop high-quality biosimilars that can cater to regulated and other markets. Currently the biosimilar pipeline includes bacterial therapeutic proteins and MAbs (monoclonal antibodies) Explore us at : Position Details: Function: Biologics, Regulatory Affairs Position: Sr. Manager- Biologics Regulatory Affairs- CMC Job Location: Govandi (East ), Mumbai (1st, 3rd, 5th Saturday working, 2nd and 4th Saturday off), Work from office) Desired Qualification: M.Pharm/B.PharmDesired Work Experience: Candidates having at Least 10- 18 years of experience in US and EU market registrations for Biosimilar therapeutic proteins and Monoclonal Antibodies Alternatively, candidates having at least 10- 18 experience in Small molecules injectables registrations for the US market with dossier authoring and query response for both drug substance and drug product.Job Responsibilities: 1. Biosimilar Regulated market submissions - US / EU regulatory submission. 2. Biosimilar Dossier Authoring (Drug substance and Drug product), MOH query response and Hands on experience in eCTD submissions 2. Biosimilar Product Development Strategy for CMC and Clinical development 3. Review of Quality documents including coordination with Cross functional teams ( R&D, QC/QA and Manufacturing) 4. Biosimilar Product Life Cycle Management 5. RA support for Plant related QMS activities