Ahmedabad 1–5 Years 5 vacancies Full Time
Key Responsibilities
- Preparation of documents: COA, MFR, Product Validation (PV), Stability Data
- Preparation of ACTD/CTD dossiers for regulatory submissions
- Artwork coordination and regulatory review
- CMC review and documentation for African, LATAM, CIS, and emerging markets
- Liaison with regulatory authorities and management teams
Requirements
- B.Pharma / M.Pharma or equivalent
- Knowledge of ACTD/CTD dossier formats
- Familiarity with regulatory markets (Africa, LATAM, CIS)
- Valuable communication & documentation skills
Send Your Application
Please send your updated CV to our HR team. Mention the position you are applying for in the subject line.
[email protected]
📌 Regulatory Affairs (India)
🏢 Vivanza Biosciences
📍 India