We are looking for a Regulatory Affairs Executive with experience in pharmaceutical regulatory documentation and product registration for international markets. The candidate will be responsible for dossier preparation, submission, and regulatory coordination for semi-regulated markets.
Key Responsibilities:
- Prepare, compile, and submit dossiers for ROW, LATAM, CIS, Africa, and Pacific markets
- Handle CTD/ACTD dossier documentation
- Support product registration and lifecycle management activities
- Coordinate with clients and internal departments for regulatory requirements
- Prepare and manage AMV and DMF documents
- Support out-licensing and regulatory projects
Requirements:
- 1 to 4 years of experience in a pharmaceutical manufacturing company
- Knowledge of regulatory documentation and international market registration
- Experience in AMV and DMF preparation preferred
- Good communication and coordination skills
Qualification:
B.Pharma / M.Pharma / B.Sc / MBA
Industry:
Pharmaceutical & Life Sciences
Pay: ₹20,000.00 - ₹30,000.00 per month
Benefits:
Work Location: In person
