Position: Sr. Executive – Regulatory Affairs
Experience: 8+ Years
Qualification: B.Pharma/M.Pharma
Job Role:
- Preparation and review of dossiers.
- Expertise in creating CTD/ACTD and country-specific dossiers.
- Knowledge of DMF/API & SF.
- Dossier preparation for tablets, capsules, creams, ointments, etc.
- Familiarity with FDA requirements, including checking PVSS data and applying for COPP/FSC.
How to Apply: Interested candidates are encouraged to share their CVs at shweta.m@titanpharma.com