Artiva Biotherapeutics Inc. in San Diego seeks a Director, MSAT, CMC & Process Validation to lead end-to-end process validation for allogeneic manufacturing, from process characterization through PPQ and continued process verification.
You will own validation strategy, author CMC sections of regulatory filings, mentor teams, coordinate across MSAT, CMC, QA, and manufacturing, and ensure readiness for Phase 3 and regulatory milestones.
#J-18808-LjbffrDirector, MSAT & CMC Process Validation - Lead PPQ & CPV in san diego at Unknown Company
This position is listed as full time and onsite.