About the role

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.

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JOB OVERVIEW

Experience level

Manager

Location

San Diego, CA

Occupation

Quality Control Systems Managers

Industry

Research and Development in Biotechnology (except Nanobiotechnology)

Posted

yesterday

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