Prepare, review, and submit DMFs/CTDs (USDMF, EDMF, CEP, etc.) for regulated and semi-regulated markets
Maintain regulatory documentation and lifecycle management of submissions
Coordinate with R&D, QA, QC, and production teams to gather data for submissions
Respond to deficiency letters from regulatory agencies
Ensure compliance with current regulatory guidelines (USFDA, EDQM, WHO, etc.)
Monitor changes in regulatory requirements and update internal teams accordingly
Support customer regulatory queries and audits
Job Types: Full-time, Permanent
Pay: ?20,000.00 - ?25,000.00 per month
Benefits:
Cell phone reimbursement
Health insurance
Paid sick time
Provident Fund
Work Location: In person
Expected Start Date: 11/08/2025
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