Quality Control Technologist I-III

Please note: The shift for this position is Tuesday-Saturday, 2:00pm-10:30pm.

What You'll Do:

• Work within a cutting-edge genomics workflow to provide quality control support in a high-volume molecular laboratory.
• Create and implement equipment functionality and reagent processes for use by Tempus R&D, clinical, and modeling lab staff while maintaining CLIA/CAP/NYS-DOH/ISO compliance.
• Complete, schedule, and track Performance Qualifications (PQs), Preventive Maintenance (PM), relocation, and routine maintenance for all laboratory equipment.
• Organize and prepare reagents prior to quality control evaluations and use. Execute and record quality control evaluations for new reagent lots for laboratory use.
• Collect and analyze QC data including phase ins, PQs, and monitoring of metrics.
• Investigate issues and facilitate the implementation of corrective and preventative actions.
• Liaise with lab management and personnel to provide training, troubleshoot issues, and prioritize QC activities.
• Report significant findings/deviations and system deficiencies to lab management, as appropriate.
• Update Standard Operating Procedures (SOPs) and equipment records within the document control system, including drafting, revision, and review of internal SOPs and other quality documentation, including but not limited to: reagent lot verifications, equipment repair field service reports, and maintenance logs.
• Navigate filing and database systems to retrieve and accurately record QC results and data.
• Participate in lab audits with QA/Pharma/regulatory bodies as needed.
• Monitor and respond to laboratory temperature excursions.
• Maintain a clean working environment and contribute to maintaining an organized laboratory.

Qualifications:

• BS in medical technology, clinical laboratory science, chemical, physical or biological science.
• Prefer at least 1+ year of previous experience in a molecular lab or with laboratory liquid handlers.
• Previous experience in a clinical lab regulated by CAP/ CLIA/ NYS/ ISO is highly desirable.
• Ability to analyze quality control data, monitor assay or instrument performance metrics.
• Strong problem-solving skills to identify and investigate issues within laboratory processes and implement corrective actions.
• Excellent communication skills for working with cross-functional teams.
• Proficiency in maintaining accurate records and managing documentation within a control system.
• Strong organizational skills with superb attention to detail and accuracy.
• Proven ability to learn new skills quickly and adapt to new processes smoothly.
• Moderate experience with Microsoft Excel and/ or Google Sheets.
• Good time management skills.
• Able to lift 40lbs occasionally, highly desirable.