Clinical Quality Assurance Associate (Life Sciences)

Tempus AI, Inc.; Chicago (IL); On-site; USD 32,000 - 39,000; Full time

Benefits offered by this job

Full range of benefits

Job summary

Tempus is seeking a Senior Quality Assurance Associate to document and track compliance for a clinical molecular laboratory. This role supports QA activities in accordance with FDA QMSR, ISO 13485, and CLIA/CAP requirements, including records management, batch records, checklists, and quality and equipment binders.

The position offers Illinois pay range of $23.00-$28.00 per hour, with the possibility of variation based on qualifications and experience.

Qualifications

• High school diploma or Bachelor's in Life Science or Engineering preferred.
• 0–2 years of experience in quality, industry, or clerical/documentation handling.
• Highly organized with superb attention to detail.
• Ability to complete repetitive tasks with precision.
• Quick learner; adapt to new processes quickly.
• Good time management and communication skills.
• Self-driven; fast-moving cross-functional environment.
• Beginner-friendly: able to create processes and suggest solutions.

Responsibilities

• Compile the 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 tracking and maintenance of quality records and binders.
• Report deviations to management under guidance.
• Pull records during audits.
• Support corrective and preventative actions.
• Assist in document control workflow.
• Manage supplier documentation and compliance.

Skills

Attention to detail

Time management

Communication skills

Documentation

Self-motivated

Cross-functional teamwork

Education

Bachelor's degree in Life Science or Engineering

High school diploma

Tools

Microsoft Office

Google Suite

Document control systems

Job description

Tempus is seeking a Senior Quality Assurance Associate to document and track compliance for a clinical molecular laboratory. This role supports QA activities in accordance with FDA QMSR, ISO 13485, and CLIA/CAP requirements, including records management, batch records, checklists, and quality and equipment binders.

The position offers Illinois pay range of $23.00-$28.00 per hour, with the possibility of variation based on qualifications and experience.