Quality & Document Control Specialist
Nucleus Biologics
Nucleus Biologics in San Diego, CA is seeking a Quality Specialist to support QA and document control within a cGMP environment. You will manage controlled documents, issue manufacturing and batch records, coordinate change requests, and support audits across functions. The ideal candidate has 2–4 years in QA/document control, knowledge of GMP/ISO/FDA, and experience with eQMS systems (ZenQMS preferred). Detail-oriented and collaborative, you will help ensure product release readiness and data #J-18808-Ljbffr Nucleus Biologics
Vacancy posted 3 days ago
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