Director, MSAT & CMC Process Validation — PPQ Leader
Listed on 2026-10-07
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Pharmaceutical
Regulatory Compliance Specialist, Validation Engineer, Quality Engineering, Pharmaceutical Manufacturing -
Manufacturing / Production
Regulatory Compliance Specialist, Validation Engineer, Quality Engineering, Pharmaceutical Manufacturing
Artiva Biotherapeutics in San Diego, CA seeks a Director, MSAT, CMC & Process Validation to lead end-to-end process validation for allogeneic manufacturing. You will own the validation lifecycle from process characterization through PPQ and continued process verification, collaborating across MSAT, CMC, Quality, and GMP Manufacturing.
The role requires hands-on PPQ execution in late-stage development, deep CMC/GMP knowledge, and leadership of cross-functional teams.
This opening is for the Director, MSAT & CMC Process Validation — PPQ Leader role at Artiva Biotherapeutics.
As a Director, MSAT & CMC Process Validation — PPQ Leader, you will play an important part at Artiva Biotherapeutics in San Diego, CA, United States.
We invite applications for the Director, MSAT & CMC Process Validation — PPQ Leader position located in San Diego, CA, United States.
The following position is for a Director, MSAT & CMC Process Validation — PPQ Leader with Artiva Biotherapeutics.
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