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Manager, Regulatory Affairs CMC with Viral Vector experience
Gilead Sciences
Hoofddorp · HybridSenior (5–10 years)Full-timePosted 17 Sep 2026
About the job
What you'll do
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.
What they're looking for
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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