Todas as vagas
Manager, Regulatory Affairs CMC with Viral Vector experience
Kite Pharma
Hoofddorp · HíbridoSênior (5–10 anos)Tempo integralPublicada em 17 de set. de 2026
Sobre a vaga
O que você vai fazer
The Regulatory Affairs CMC Lead will manage regulatory deliverables for clinical and commercial cell therapy programs while developing and executing CMC regulatory strategies. They will also provide guidance to cross-functional teams and ensure compliance with international regulatory requirements for ATMPs.
O que eles procuram
Candidates must have at least 8 years of experience in Regulatory Affairs or a relevant industry, with specific expertise in viral vectors or lipid nanoparticles. An advanced degree such as a PhD or MS is highly desired, along with strong communication skills and the ability to influence stakeholders.
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