Responsible for ANVISA regulatory submissions, eCTD dossier management, multi-market regulatory activities, audit handling, and compliance with global regulatory guidelines.
Required Candidate profile
M.Pharm/M.Sc with 3–8 years of experience in Regulatory Affairs. Robust knowledge of ANVISA submissions, eCTD, dossier compilation, global regulatory guidelines, audit handling, &lifecycle; management.
📌 Senior Regulatory Affairs Executive Navi Mumbai (India)
🏢 Great Pacific Exports
📍 India
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