About the role
Work within a cutting-edge genomics workflow to provide equipment quality control support in a high-volume clinical molecular laboratory. Help create and implement new equipment functionality for use by Tempus R&D and clinical lab staff while maintaining CLIA/CAP/ISO compliance. Complete Performance Qualifications (PQs), Preventive Maintenance (PM), relocation, and routine maintenance for all clinically approved molecular laboratory equipment. Collect and help analyze metrics. Investigate equipment related issues and help facilitate and implement corrective and preventative actions. Interact with lab management and personnel to provide training, troubleshoot issues, and prioritize QC tasks. Report significant findings/deviations and system deficiencies to lab management, as appropriate. Update SOPs and equipment records within the document control system, including creation/ revision/ review of internal SOPs and other quality documentation. Create and review protocols and qualification summaries. Support the Lab Facilities team with freezer defrosts and hazardous waste pick-up as needed. Monitor and respond to laboratory temperature excursions.