Clinical Genomics QA Associate | Lab Compliance
Tempus
Tempus, a Chicago-based company advancing precision medicine, seeks a Senior Quality Assurance Associate or QA Specialist to document and track compliance for a clinical molecular laboratory under FDA QMSR, ISO 13485, CLIA/CAP. Shifts: Sun–Thu or Tue–Sat. The role supports QMS activities, maintains records, and works with suppliers to ensure up-to-date documentation; corporate benefits are provided. #J-18808-Ljbffr Tempus
Vacancy posted 3 days ago
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