Nucleus Biologics, The Cell Performance Company, San Diego, CA, is seeking a Quality Specialist to support QA and document control within a cGMP environment. You will manage controlled documents, release manufacturing and batch records, oversee change requests, and assist audits.
The role requires 2–4 years in QA/document control, familiarity with GMP/ISO/FDA standards, and experience with eQMS (ZenQMS preferred). Strong attention to detail and cross-functional collaboration are essential.
