- Good communication and teamwork abilities.
- Basic understanding of regulatory affairs in the pharmaceutical industry.
- Strong documentation and organizational skills.
- Knowledge of CTD/eCTD submissions is a plus.
- Assist in the preparation and submission of regulatory documents, including dossiers for product registrations, variations, and renewals.
- Support in collecting and organizing technical data to ensure regulatory compliance.
- Help in maintaining regulatory databases and tracking the status of submissions and approvals.
- Coordinate with cross-functional teams to ensure timely regulatory filings.
- Basic knowledge of IFP, FASSAI, FDCA & Sugam Portal for preparation and application for permission, License, COPP, FSC, NOC etc..
Job Types: Full-time, Fresher
Pay: ₹180,000.00 - ₹240,000.00 per year
Work Location: In person
