Quality Assurance Document Control Specialist
Artiva Biotherapeutics
Artiva Biotherapeutics in San Diego seeks a QA Document Control professional with 3+ years of GMP/regulatory experience to manage document lifecycle, training records, and controlled labeling using the eQMS. This role supports inspection readiness and records management across QA Operations. You will review change requests, administer the eQMS, onboard new hires with training curricula, and coordinate labeling records while ensuring compliance with FDA, ISO, and company procedures. #J-18808-Ljbffr Artiva Biotherapeutics
Vacancy posted 2 days ago
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