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Director, Regulatory Affairs
OCUGEN OPCO INC
Amsterdam · PresencialLiderança (10+ anos)OutroPublicada há 8 dias
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O que você vai fazer
The Director will lead regulatory strategy and execution for gene therapy and ATMP programs across the EU and UK, managing interactions with the EMA and MHRA. They will provide strategic guidance throughout the product lifecycle and coordinate regulatory activities across cross-functional global teams.
O que eles procuram
Candidates must have 10+ years of regulatory experience in biotechnology, specifically with innovative biologics, cell therapy, or gene therapy. An advanced degree in a relevant scientific or medical discipline is preferred, along with demonstrated experience in late-stage clinical development and major regulatory submissions.
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