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Tempus

AI-driven platform for medical data insights

Quality Control Technologist 1-3

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeChicago, IL, USAIn-person

About the Job

Requirements

  • A Bachelor of Science in medical technology, clinical laboratory science, chemical science, physical science, or biological science is required.
  • The ability to analyze quality-control data and monitor assay or instrument performance metrics is required.
  • The ability to investigate laboratory-process issues and implement corrective actions is required.
  • Proficiency in maintaining accurate records and managing documentation within a control system is required.
  • Moderate experience with Microsoft Excel and/or Google Sheets is required.
  • The role requires the ability to lift 40 pounds occasionally.

Responsibilities

  • Maintain equipment and reagent compliance in Tempus laboratories.
  • Work within a high-volume molecular laboratory genomics workflow to provide quality-control support.
  • 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, and ISO compliance.
  • Complete, schedule, and track Performance Qualifications (PQs), Preventive Maintenance (PM), equipment relocation, and routine maintenance for all laboratory equipment.
  • Organize and prepare reagents before quality-control evaluations and use, and execute and record quality-control evaluations for new reagent lots for laboratory use.
  • Collect and analyze quality-control data, including phase-ins, Performance Qualifications, and monitoring metrics.
  • Investigate issues and facilitate implementation of corrective and preventative actions.
  • Liaise with lab management and personnel to provide training, troubleshoot issues, and prioritize quality-control activities.
  • Report significant findings, deviations, and system deficiencies to lab management as appropriate.
  • Update Standard Operating Procedures and equipment records within the document control system, including drafting, revising, and reviewing internal SOPs and other quality documentation such as reagent lot verifications, equipment repair field service reports, and maintenance logs.
  • Use filing and database systems to retrieve and accurately record quality-control results and data.
  • Participate in laboratory audits with QA, pharmaceutical, and regulatory bodies as needed.
  • Monitor and respond to laboratory temperature excursions.
  • Maintain a clean working environment and contribute to an organized laboratory.

Desired Qualifications

  • At least one year of previous experience in a molecular laboratory or with laboratory liquid handlers is preferred.
  • Previous experience in a clinical laboratory regulated by CAP, CLIA, NYS, or ISO is highly desirable.

About the Company

Tempus

AI-driven platform for medical data insights

Tempus uses AI and data analytics to improve patient care and accelerate drug development in healthcare. Its proprietary platform analyzes medical data and images to provide actionable insights for physicians and to identify gaps in care, while helping pharma and biotech companies discover targets and evaluate treatments. Cancer research is a focus, including a pan-cancer organoid platform for precision medicine and a liquid biopsy assay to profile circulating tumor DNA. Revenue comes from providing platform access and insights to healthcare providers and industry partners, with the goal of advancing personalized medicine and speeding cancer research.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Chicago, IL
Founded
2015

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