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Director, MSAT & CMC Process Validation - Lead PPQ & CPV

Job in San Diego, San Diego County, California, 92189, USA
Listing for: Artiva Biotherapeutics Inc.
Full Time position
Listed on 2026-08-26
Job specializations:
  • Pharmaceutical
    Regulatory Compliance Specialist, Validation Engineer, Quality Engineering, Pharmaceutical Manufacturing
  • Manufacturing / Production
    Regulatory Compliance Specialist, Validation Engineer, Quality Engineering, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 180000 - 250000 USD Yearly USD 180000.00 250000.00 YEAR
Job Description & How to Apply Below

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.

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