Opening for Position RA Executive with experience of 1 Year to 2 years. Freshers will also be considered.
Qualification: B.Pharm / M.Pharm.
Key Responsibilities & Technical Requirements:
- Preparation, compilation, review, and maintenance of regulatory dossiers for international markets.
- Exposure to regulatory submissions for ASEAN, LATAM, and African countries will be preferred.
- Working knowledge of regulatory documents such as:
- CDP (Common Dossier Package)
- RMP (Risk Management Plan)
- AMV and other country-specific regulatory requirements
- Understanding of country-specific registration guidelines, authority requirements, submission formats, regulatory checklists, and timelines.
- Preparation and review of CTD/ACTD dossiers and related regulatory documentation.
- Coordination with overseas clients, regulatory authorities, and manufacturing partners.
- Management of international product registrations and lifecycle maintenance activities.
- Identification of new business opportunities and support for business development initiatives.
- Follow-up on quotations, agreements, registrations, commercial discussions, and client communications.
- Maintenance and strengthening of client relationships through effective coordination and communication.
Pay: ₹18,000.00 - ₹30,000.00 per month
Benefits:
Work Location: In person
