Todas as vagas
Manager, Regulatory Affairs CMC with Viral Vector experience
Gilead Sciences
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 clinical and commercial cell therapy programs by developing regulatory strategies and ensuring high-quality CMC documentation. They will also provide guidance to cross-functional teams and interpret international regulatory requirements to support product lifecycle management.
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.
Descrição completa