23 Oct
|
Flamingo Pharmaceuticals
|
Navi Mumbai
23 Oct
Flamingo Pharmaceuticals
Navi Mumbai
Lead regulatory submissions for tablets and capsules in USFDA, MHRA, EU and UK markets. Manage CTD/eCTD dossiers, product registrations, pre- and post-approval changes, regulatory queries, compliance, and team coordination to ensure timely approvals.
Required Candidate profile
B.Pharm/M.Pharm with 6–10 years’ Regulatory Affairs experience in tablets and capsules, handling USFDA, MHRA, EU/UK markets, CTD/eCTD dossiers, product registration, variations, and team management.
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