Quality Assurance Document Control Specialist II
Artiva Biotherapeutics
Artiva Biotherapeutics is seeking a Quality Assurance Operations professional to support document control, records management, and training administration in a GMP environment. You will oversee controlled documents, training records, labeling activities, and related quality records to ensure accuracy, traceability, and readiness for audits. The role emphasizes digitization of records, compliance with FDA/ISO standards, and collaboration with internal teams to maintain inspection readiness in a #J-18808-Ljbffr Artiva Biotherapeutics
Vacancy posted 1 day ago
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