Quality Control Reagents I - IV
Tempus AI
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Raleigh-Durham-Chapel Hill Area
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Entry level
Posted March 4, 2026
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Responsibilities
Responsibilities
- Work within a cutting-edge genomics workflow to provide quality control support in a
- high-volume clinical molecular laboratory.
- Test and document new lots of reagents for clinical lab team processing and label
- reagents approved for use.
- Maintain reagent qualification records and manage quality control of reagent inventory.
- Document all results and findings in order to satisfy CLIA/CAP/NYS-DOH/ISO
- compliance.
- Collect and help analyze metrics.
- Investigate reagent related issues and help facilitate and implement corrective and
- preventative actions.
- Interact with lab management and personnel to provide training, troubleshoot issues,
- and prioritize QC tasks.
- Report significant findings/deviations and system deficiencies to lab management, as
- appropriate.
- Update SOPs and records within the document control system, including creation/
- revision/ review of internal SOPs and other quality documentation.
- Complete Performance Qualifications (PQs) and support the Lab QC team with
- equipment and documentation tasks as needed.
- Monitor and respond to laboratory temperature excursions.
Not Met Priorities
What still needs stronger evidence
Requirements
- Highly organized and systematic, superb attention to detail and ability to complete tasks
- with a high degree of accuracy.
- Proven ability to learn new skills quickly and adapt to new processes smoothly.
- science.
- handlers.
- Moderate experience with Microsoft Excel and/ or Google Sheets.
- Previous experience in a clinical lab regulated by CAP/ CLIA/ NYS/ ISO is highly
Preferred Skills
- ○ Prefer 1 year previous experience in a molecular lab or with laboratory liquid
- Moderate experience with Microsoft Excel and/ or Google Sheets.
- Previous experience in a clinical lab regulated by CAP/ CLIA/ NYS/ ISO is highly
- Good time management skills.
- Excellent communication skills.
Education
- (Not required) – BS in medical technology, clinical laboratory science, chemical, physical or biological
- (Not required) – science.
Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
Responsibilities
Work within a cutting-edge genomics workflow to provide quality control support in a
high-volume clinical molecular laboratory.
Test and document new lots of reagents for clinical lab team processing and label
reagents approved for use.
Maintain reagent qualification records and manage quality control of reagent inventory.
Document all results and findings in order to satisfy CLIA/CAP/NYS-DOH/ISO
compliance.
Collect and help analyze metrics.
Investigate reagent related issues and help facilitate and implement corrective and
preventative actions.
Interact with lab management and personnel to provide training, troubleshoot issues,
and prioritize QC tasks.
Report significant findings/deviations and system deficiencies to lab management, as
appropriate.
Update SOPs and records within the document control system, including creation/
revision/ review of internal SOPs and other quality documentation.
Complete Performance Qualifications (PQs) and support the Lab QC team with
equipment and documentation tasks as needed.
Monitor and respond to laboratory temperature excursions.
Qualifications
Highly organized and systematic, superb attention to detail and ability to complete tasks
with a high degree of accuracy.
Proven ability to learn new skills quickly and adapt to new processes smoothly.
BS in medical technology, clinical laboratory science, chemical, physical or biological
science.
○ Prefer 1 year previous experience in a molecular lab or with laboratory liquid
handlers.
Moderate experience with Microsoft Excel and/ or Google Sheets.
Previous experience in a clinical lab regulated by CAP/ CLIA/ NYS/ ISO is highly
desirable.
Good time management skills.
Excellent communication skills.
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
Responsibilities
Work within a cutting-edge genomics workflow to provide quality control support in a
high-volume clinical molecular laboratory.
Test and document new lots of reagents for clinical lab team processing and label
reagents approved for use.
Maintain reagent qualification records and manage quality control of reagent inventory.
Document all results and findings in order to satisfy CLIA/CAP/NYS-DOH/ISO
compliance.
Collect and help analyze metrics.
Investigate reagent related issues and help facilitate and implement corrective and
preventative actions.
Interact with lab management and personnel to provide training, troubleshoot issues,
and prioritize QC tasks.
Report significant findings/deviations and system deficiencies to lab management, as
appropriate.
Update SOPs and records within the document control system, including creation/
revision/ review of internal SOPs and other quality documentation.
Complete Performance Qualifications (PQs) and support the Lab QC team with
equipment and documentation tasks as needed.
Monitor and respond to laboratory temperature excursions.
Qualifications
Highly organized and systematic, superb attention to detail and ability to complete tasks
with a high degree of accuracy.
Proven ability to learn new skills quickly and adapt to new processes smoothly.
BS in medical technology, clinical laboratory science, chemical, physical or biological
science.
○ Prefer 1 year previous experience in a molecular lab or with laboratory liquid
handlers.
Moderate experience with Microsoft Excel and/ or Google Sheets.
Previous experience in a clinical lab regulated by CAP/ CLIA/ NYS/ ISO is highly
desirable.
Good time management skills.
Excellent communication skills.
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.