Biologics, Regulatory Affairs- CMC

About the Company

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 specialise in niche product areas across international markets, including Oral Solid Dosages (OSD), sterile products, peptides, biologics, and oncology. USVs 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 :

About the Role

Function: Biologics, Regulatory Affairs

Position: Deputy Manager/Manager/Senior Manager - Biologics Regulatory Affairs- CMC

Job Location: Govandi (East), Mumbai (1st, 3rd, 5th Saturday working, 2nd and 4th Saturday off), Work from office only

Must Haves:

A minumum of 4 years experience in the below:

US & EU registration for Biosimilars

Regulatory experience for both drug substance and drug product for USFDA and EMA

Intial dossier authoring for modules I - III of CMC for EU & US

Biosimilar filing for EU & US

Authoring pre approval dossiers for US and EU.

MOH query response for both Drug Substance and Drug Product.

If from Small Molecules

Strong xperience in Small Molecule Injectables registrations for the US market

Strong experience in MOH query response for both Drug Substance and Drug Product.

Qualifications

• Desired Qualification: M.Pharm/B.Pharm
• Desired Work Experience: Candidates having at least 6 - 10 years of experience in US and EU market registrations for Biosimilar therapeutic proteins and Monoclonal Antibodies. Alternatively, candidates having at least 8 - 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.

Responsibilities

• Biosimilar Regulated market submissions - US / EU regulatory submission.
• Biosimilar Dossier Authoring (Drug substance and Drug product), MOH query response and Hands on experience in eCTD submissions.
• Biosimilar Product Development Strategy for CMC and Clinical development.
• Review of Quality documents including coordination with Cross functional teams (R&D, QC/QA and Manufacturing).
• Biosimilar Product Life Cycle Management.
• RA support for Plant related QMS activities.