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Capa Quality Assurance Jobs (NOW HIRING)

Tempus

Quality Assurance Specialist

Chicago, IL · On-site

$55K - $70K/yr

The Quality Assurance Specialist plays an integral role in supporting quality activities related to ... Participate if needed as a NC and CAPA subject matter expert during internal and external audits.

Care Access

Specialist, Quality Assurance

OR · On-site +1

The QA specialist will directly support quality initiatives, audit functions, CAPA systems and promote inspections readiness. Working in support of the Associate Director of Quality Assurance, the ...

Sanmina

QA Engineer

San Jose, CA · On-site

$80K - $90K/yr

The ideal candidate is skilled in root cause investigations, corrective actions (CAPA), and ... Core Qualifications Quality Assurance & Manufacturing Quality Systems Incoming, In-Process, and ...

Peak Nano

Quality Assurance Manager

Valley View, OH · On-site

The Quality Assurance Manager leads initiatives such as CAPA implementation, document control, internal audits, management reviews, quality metrics, and preparation for ISO certification, ensuring ...

Care Access

Specialist, Quality Assurance

Boston, MA

The QA specialist will directly support quality initiatives, audit functions, CAPA systems and promote inspections readiness. Working in support of the Associate Director of Quality Assurance, the ...

Tempus

Quality Assurance Specialist

Chicago, IL · On-site

$55K - $70K/yr

The Quality Assurance Specialist plays an integral role in supporting quality activities related to ... Participate if needed as a NC and CAPA subject matter expert during internal and external audits.

Care Access

Specialist, Quality Assurance

The QA specialist will directly support quality initiatives, audit functions, CAPA systems and promote inspections readiness. Working in support of the Associate Director of Quality Assurance, the ...

Zunch Staffing

Quality Assurance Manager

Nashville, TN · On-site

$75K - $90K/yr

Conduct internal audits and manage Corrective and Preventive Action (CAPA) processes. * People Management: Supervise and lead Quality Assurance Technicians and Quality Control Technicians.

Bimeda Inc.

QA Associate

Pomona, CA · On-site

$82K - $113K/yr

Provide oversight and QA approval for CAPA, deviation, and change control systems; monitor quality history and trends, and recommend data-driven improvements. * Lead change control initiatives and ...

Bimeda, Inc.

QA Associate

Pomona, CA · On-site

Provide oversight and QA approval for CAPA, deviation, and change control systems; monitor quality history and trends, and recommend data-driven improvements. * Lead change control initiatives and ...

Bimeda Inc.

QA Associate

Pomona, CA

Provide oversight and QA approval for CAPA, deviation, and change control systems; monitor quality history and trends, and recommend data-driven improvements. * Lead change control initiatives and ...

ProCaps Labs

QA Compliance Supervisor

Henderson, NV · On-site

The Quality Assurance Compliance Supervisor is responsible for supervising and coordinating the ... Experience with CAPA, deviations, and customer complaints preferred * Detail-oriented, with ...

ProCaps Labs

QA Compliance Supervisor

Henderson, NV · On-site

The Quality Assurance Compliance Supervisor is responsible for supervising and coordinating the ... Experience with CAPA, deviations, and customer complaints preferred * Detail-oriented, with ...

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Capa Quality Assurance information

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How much do capa quality assurance jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for capa quality assurance in the United States is $23.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $24.28 per hour, depending on experience, location, and employer.

What is CAPA Quality Assurance?

Capa Quality Assurance refers to the processes and practices used to ensure that products and services meet regulatory and organizational quality standards, particularly through the Corrective and Preventive Action (CAPA) system. CAPA is a critical component in industries like pharmaceuticals, medical devices, and manufacturing, where it helps identify, investigate, and resolve quality issues to prevent their recurrence. Quality Assurance professionals in CAPA are responsible for monitoring compliance, analyzing root causes of problems, and implementing solutions to improve overall product quality and safety.

How does a CAPA Quality Assurance professional collaborate with other departments to address quality issues?

As a CAPA Quality Assurance professional, you will regularly work with cross-functional teams such as manufacturing, engineering, and regulatory affairs to investigate, document, and resolve quality issues. Collaboration often involves facilitating root cause analysis meetings, reviewing corrective and preventive action plans, and ensuring timely implementation of solutions. Effective communication and project management skills are essential, as you must coordinate with various stakeholders to monitor progress and verify that actions have successfully mitigated the identified risks.

What are the key skills and qualifications needed to thrive as a CAPA Quality Assurance professional?

To thrive as a CAPA Quality Assurance professional, you need a solid understanding of quality management systems, regulatory compliance, root cause analysis, and typically a degree in a scientific or engineering field. Familiarity with CAPA management software, ISO standards (such as ISO 13485 or ISO 9001), and documentation tools is often required. Strong attention to detail, analytical thinking, and effective communication are crucial soft skills for investigating issues and implementing solutions. These competencies ensure that process failures are thoroughly addressed and prevented, maintaining product quality and regulatory compliance.

What is the difference between Capa Quality Assurance vs Quality Control Inspector?

AspectCapa Quality AssuranceQuality Control Inspector
Primary FocusPreventive measures, process improvement, ensuring compliance with CAPA proceduresDetecting defects, inspecting products, verifying quality at various stages
CredentialsISO certifications, quality assurance training, knowledge of CAPA processesQuality inspection certifications, technical skills in product testing
Work EnvironmentDocumentation review, process audits, collaboration with production teamsOn-site inspections, sampling, testing products or components
Industry UsageManufacturing, pharmaceuticals, medical devices

While Capa Quality Assurance focuses on preventing issues through process improvements and CAPA procedures, Quality Control Inspectors primarily identify defects through product inspections. Both roles are essential for maintaining quality but differ in their approach and scope within the quality management system.

What are popular job titles related to Capa Quality Assurance jobs?

For Capa Quality Assurance jobs, the most frequently searched job titles are:

Infographic showing various Capa Quality Assurance job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $48,237 per year, or $23.2 per hour.

Quality Assurance Specialist

Chicago, IL • On-site

Tempus
See more jobs at Tempusexternal

$55K - $70K/yr

Full-time

Re-posted 7 days ago

Job description

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.

Please note: This position is onsite in Chicago and requires you to work Tuesday-Saturday or Sunday-Thursday.

The Quality Assurance Specialist plays an integral role in supporting quality activities related to incidents and issues, including deviations, nonconformances (NC) and corrective and preventive actions (CAPA) in accordance with FDA QSR (Quality System Regulation), ISO 13485, and other applicable global regulations. This individual also supports the QMS activities that comply with CLIA/CAP requirements for the clinical laboratories.

Responsibilities include the following. Other duties may be assigned.

  • Responsible for processing and managing issues/incidents that include deviations, NCs, and CAPAs, as well as ensuring compliance to FDA 21 CFR 820, ISO 13485, CAP/CLIA and other applicable quality system regulations and standards.

  • Participate in process improvements to the issue/incident reporting framework by helping identify areas for improvement, simplification, and standardization, ensuring that the various systems are streamlined and aligned.

  • Collaborate with Regulatory on appropriate health authority reporting, as necessary.

  • Assist in NC/CAPA activities, including investigations, root cause analysis, effectiveness verification, and closure by establishing cross-functional relationships and collaborations with functional owners.

  • Drive ownership of issues/incidents to lead to final resolution and closure by providing training and guidance to owners.

  • Responsible for assisting in activities to ensure departmental goals for deviations, NC and CAPA processes are achieved.

  • Identify trends and provide metrics to drive root cause analysis and corrective actions to prevent the recurrence of quality issues

  • Participate if needed as a NC and CAPA subject matter expert during internal and external audits.

  • Lead and/or support other duties as assigned.

Required Education & Experience:

  • Bachelor's Degree in Engineering or Science field.

  • 1 to 3+ years of QA experience in a clinical laboratory/medical device/Diagnostic company.

  • Working knowledge of medical device / in vitro diagnostic regulations (e.g., FDA 21 CFR 820, ISO 13485, IVDD, and other applicable quality and regulatory standards).

  • QA experience in a clinical molecular testing laboratory (LDTs) is required.

  • Working knowledge of the deviations, NC and CAPA processes.

  • Strong communication (written and verbal), influencing, negotiating and collaboration skills.

  • Ability to work through complex issues and differences in a creative, constructive, and diplomatic manner.

  • Ability to manage multiple tasks with limited supervision.

  • Ability to demonstrate leadership in helping improve quality processes and create efficiencies for business needs.

  • Ability and willingness to work independently and take initiative to ensure timely action on issues.

  • This will be an on-site position.

Illinois Pay Range: $55,000-$70,000


The expected salary range may vary for other locations. Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

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.

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