Allogene Therapeutics seeks a Senior Director, CMC Regulatory Affairs in South San Francisco. This hybrid role leads CMC regulatory strategy and directs regulatory submissions for CAR T programs, ensuring alignment with Health Authority expectations and on-time delivery. You will coordinate with manufacturing, QA, and supply chain teams across regulatory plans and inspections. The role requires strong leadership, deep expertise in CMC, and a proven track record in global regulatory submissions

Also on the board Same function, level within a rung

Level

Manager

Location

South San Francisco, CA

Occupation

Regulatory Affairs Managers

Industry

Biological Product (except Diagnostic) Manufacturing

Posted

yesterday

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