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Director, MSAT & CMC Process Validation — PPQ Leader

Job in San Diego, San Diego County, California, 92189, USA
Listing for: Artiva Biotherapeutics
Full Time position
Listed on 2026-08-25
Job specializations:
  • Manufacturing / Production
    Validation Engineer, Regulatory Compliance Specialist, Pharmaceutical Manufacturing, Quality Engineering
  • Pharmaceutical
    Validation Engineer, Regulatory Compliance Specialist, Pharmaceutical Manufacturing, Quality Engineering
Salary/Wage Range or Industry Benchmark: 210000 - 270000 USD Yearly USD 210000.00 270000.00 YEAR
Job Description & How to Apply Below

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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