Director, MSAT & CMC Process Validation - Lead PPQ & CPV
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 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.
Our organisation is growing, and we are hiring a Director, MSAT & CMC Process Validation - Lead PPQ & CPV in San Diego, CA, United States.
All applications are reviewed carefully by our team.
The position is based in San Diego, CA, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Engineering.
The advertised compensation is 180..
We aim to respond to suitable candidates as soon as possible.
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