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Regulatory Affairs Manager
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Full-time
- Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies.
- Managing regulatory compliance activities for Kindeva and existing customer products and registrations as required and providing strategic planning for regulatory changes.
- E.g., IND feedback, MAA project feedback, Pre IND meeting outcomes to ensure continuous improvement.
- Advising on CMC elements of variation / supplement packages as required.
- Graduate in pharmacy or a life science (or equivalent).
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