Title: Executive
Date:
Apr 15, 2024
Location:
Tandalja - R&D
Company:
Sun Pharmaceutical Industries Ltd
- Review all data and documents related to product registrations for various health authorities.
- Compile registration dossiers for submission to various health authorities like – USA, Canada, Europe, Australia and Israel.
- Prepare responses to deficiency letters received from various agencies.
- Maintain life-cycle / post approval changes for drug product registration dossiers.
- Provide regulatory support to cross functional departments.
- Prepare and submit scientific advice to various health authorities.
- eCTD compilation, verification and submission through electronic gateway