HEAD RA ( CMC)

Job Description : HEAD RA ( CMC) IRELAND Open to International candidates 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 :www.usvindia.com Desired Work Experience: Candidates having at Least 20+ years of experience in US and EU market registrations for Biosimilar therapeutic proteins and Monoclonal Antibodies Alternatively, candidates having at least 6 - 10 years of 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

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