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Posted:2 months ago| Platform: 
Work from Office
Full Time
Key Responsibilities: Preparation and submission of DMF (Drug Master Files) and other regulatory documents. Handling regulatory queries and compliance with global regulatory agencies. Coordination with R&D, QA, and production teams for regulatory submissions. Maintaining up-to-date knowledge of regulatory guidelines (USFDA, EDQM, TGA, etc.). Ensuring smooth regulatory approvals and post-approval compliance.
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