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Job description
Sentibio in South San Francisco seeks a regulatory affairs leader to drive CMC strategies for a complex cell therapy program. You will shape global regulatory CMC plans, coordinate type B/C/D meetings, and ensure alignment with agency expectations across the organization.
The role requires a BA/BS in a scientific field and 10+ years in regulatory, with extensive experience in biologics and gene/cell therapy. Some travel (approx. 20%) is expected, and VP-level reporting possibilities may exist.
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Worksite address
south san francisco, CA, 94083, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.