Biophore India Walk-In Interviews for Regulatory Affairs
API REGULATORY AFFAIRS (Preferably Male only)
Exp: 1-4 Years.
Qualification: MSc. or M Pharmacy.
JOB RESPONSIBILITIES:
1. Coordination with manufacturing plants and other departments for timely submission of Documents to the regulatory body.
2. Compilation and/or review of CTD/ e-CTD formats and ensuring documents as per the requirements proposed by US/EU regulatory bodies.
3. Compilation, submission and management of life cycle for dossiers through applicable annual updates and amendments.
4. Responding/assisting for customer queries/regulatory queries related to DMFs.
5. Supporting regulatory team for better traceability, archival of documents, training etc.
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