Quality Assurance Associate – Clinical Genomics

Tempus AI

Chicago (IL)

On-site

USD 32,000 - 36,000

Full time

15 hours ago
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Benefits offered by this job

Incentive compensation
RSUs
Medical benefits

Job summary

Tempus AI is seeking a Senior Quality Assurance Associate or Quality Assurance Associate to document and track compliance for a clinical molecular laboratory. The role supports QA activities per FDA QMSR, ISO 13485, and CLIA/CAP requirements, including records management and production controls.

The shift options are Sunday-Thursday or Tuesday-Saturday and the company offers a full range of benefits and opportunities in a fast-moving, cross-functional team environment.

Qualifications

  • High school diploma or Bachelor’s degree in Life Science or Engineering preferred.
  • 0–2 years of experience in industry or quality or with clerical/documentation handling.
  • Highly organized and systematic with superb attention to detail.
  • Ability to complete repetitive tasks with precision and accuracy.
  • Proven ability to learn new skills quickly and adapt to new processes.

Responsibilities

  • Compile Device History Record.
  • Read and understand SOPs in the document control system.
  • File quality records in an organized manner.
  • Maintain documentation to satisfy CLIA/CAP/NYS-DOH/FDA requirements.
  • Assist in tracking quality records, batch records, checklists, and equipment binders.
  • Report deviations to management and support internal audits.
  • Pull records and reports during audits.
  • Support corrective and preventive actions.

Skills

Highly organized
Attention to detail
Time management
Communication skills
Fast learner
Cross-functional teamwork
Self-driven

Education

Bachelor's Degree in Life Science or Engineering preferred

Tools

Microsoft Office / Google Suite

Job description

Tempus AI is seeking a Senior Quality Assurance Associate or Quality Assurance Associate to document and track compliance for a clinical molecular laboratory. The role supports QA activities per FDA QMSR, ISO 13485, and CLIA/CAP requirements, including records management and production controls.

The shift options are Sunday-Thursday or Tuesday-Saturday and the company offers a full range of benefits and opportunities in a fast-moving, cross-functional team environment.

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