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.
#J-18808-LjbffrDirector, MSAT & CMC Process Validation — PPQ Leader in san diego at Unknown Company
This position is listed as full time and onsite.