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