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