Job Summary
- Review and Compilation of Drug Master Files, Registration Dossiers & Technical Data Packages/Open Parts for In-House developed APIs and ensuring their updation.
- Preparation of Regulatory Amendments / Variations for smooth API supplies
- Preparation of responses to regulatory deficiencies received from Agency\'s and customer.
- Regulatory support to Chemical Research Department, Analytical Department, Chemical manufacturing, Quality Assurance, Procurement Team and Regulatory Affairs-Pharma.
- Ensure reposition of regulatory database and compliance to departmental guidelines.
- Ensuring timely Regulatory Notificaitons to Manufacturing locations.
MNCJobsIndia.com will not be responsible for any payment made to a third-party. All Terms of Use are applicable.