Tempus AI→
Quality Control Technologist I at Tempus AI in Chicago, IL
Entry LevelOn-siteFull-timeChicago, IL$48k–$48k/yr
Skills
molecular laboratory experiencequality control data analysisclia/cap/nys-doh/iso compliancemicrosoft exceldocumentation managementproblem-solving skillscommunication skillsorganizational skillstime management skillsattention to detail
Job Description
Summary: Tempus AI is focused on precision medicine and advancing the healthcare industry through AI technology. They are seeking a Quality Control Technologist I to provide quality control support in a high-volume molecular laboratory, ensuring compliance and implementing quality processes.
Responsibilities:
- 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
Required Qualifications:
- BS in medical technology, clinical laboratory science, chemical, physical or biological science
- 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
Preferred Qualifications:
- 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
- Able to lift 40lbs occasionally, highly desirable
Required Skills: Molecular laboratory experience, Quality control data analysis, CLIA/CAP/NYS-DOH/ISO compliance
Important Skills: Microsoft Excel, Documentation management
Nice-to-Have Skills: Problem-solving skills, Communication skills, Organizational skills, Time management skills, Attention to detail
Benefits: Incentive compensation, Restricted stock units, Medical and other benefits depending on the position
Benefits
Incentive compensation
Restricted stock units
Medical and other benefits depending on the position