Brief Job Description:
- Review Data and Documents:
- Review all data and documents related to product registrations for various health authorities.
- Compile Registration Dossiers:
- Compile registration dossiers for submission to various health authorities including US-FDA, Health Canada, Europe, Australia/New Zealand, Japan, and Israel.
- Prepare Responses:
- Prepare responses to deficiency letters received from various agencies.
- Maintain life-cycle/post-approval changes for drug product registration dossiers.
- Regulatory Support:
- Provide regulatory support to cross-functional departments.
- Scientific Advice Preparation:
- Prepare and submit scientific advice to various health authorities.
- eCTD Compilation:
- Compile, verify, and submit eCTD through electronic gateway.
How to Apply:
Send your resume to: Hr.tandalja@sunpharma.com
Join our team at Sun Pharma and contribute to our mission of providing high-quality healthcare solutions globally!
