Posted:3 weeks ago|
Platform:
On-site
Full Time
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 Application Deadline: 05/07/2025
Novopharm Formulation
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