Senior QA Specialist — Genomics Clinical Lab
Tempus
Tempus in Illinois is seeking a Quality Assurance Specialist or Senior QA Specialist to document and track compliance for a clinical molecular laboratory, aligning with FDA QMSR, ISO 13485, CLIA/CAP, and NYS-DOH requirements. You will manage document control, device history records, supplier documentation, and audits, while driving CAP/CLIA compliance and continuous QA improvements. The role involves converting quality data into actionable insights, coordinating with cross-functional teams, and #J-18808-Ljbffr Tempus
Vacancy posted 2 days ago
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