Clinical Genomics QA Specialist | Precision Lab Compliance
Tempus
Tempus is seeking a Senior Quality Assurance Associate or Quality Assurance Specialist to document and track compliance for a clinical molecular laboratory. The role supports QMS activities that comply with CLIA/CAP and FDA requirements, with shifts Sunday-Thursday or Tuesday-Saturday. Responsibilities include device history records, SOP review, and maintaining quality documentation. Preferred candidates have foundational lab/regulatory experience and strong organizational skills within a #J-18808-Ljbffr Tempus
Vacancy posted 1 day ago
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