Key Responsibilities:
- Should have 2 Years of Experience in Regulatory Affairs
- Coordinate with Plant and associated departments to facilitate the dossier requirements.
- Review of PVP PVR, Stability, PDR, BMR, and other directly or indirectly linked Quality Section in CTD/ACTD
- Experience in handling markets like African Countries, the Philippines, Russia (CIS), Sri Lanka, etc are preferred.
- Preparing Dossiers, Review and Filling Dossiers.
- Registration in Semi Regulated and Regulated Markets.
- Checking Artworks of Pharmaceutical Products and performing artwork modification as per Country requirements.
Pay: ₹20,000.00 - ₹23,000.00 per month
Schedule:
- Day shift
Application Question(s):
- What is your current CTC?
- What is your expected CTC?
- In how many days you can join this role?