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Regulatory Affairs Executive-Reputed Drug Manufacturing Industry-Hyderabad, Telngana, India-4 lakhs- Vishal
3 months ago
1.Review all data and documents related to product registrations for various health authoritiesCompilation of Drug Master Files
- Registration Dossiers & Technical Data Packages/OpenParts
- In-House developed APIs manufactured at In-House API manufacturing sites and ensuring their updation.
- Prepare responses to deficiency letters received from various agencies for expeditious approval.
- Preparation of Regulatory Amendments / Variations for smooth API supplies.
- Provide regulatory support to cross functional departments.
- Re-position of regulatory database and compliance to procedures
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