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Capa Jobs in Oregon (NOW HIRING)

Build success validation frameworks to confirm that CAPA actions and process improvements produce measurable, sustained outcomes - not just short-term fluctuations. * Develop performance attribution ...

Build success validation frameworks to confirm that CAPA actions and process improvements produce measurable, sustained outcomes - not just short-term fluctuations. * Develop performance attribution ...

Build success validation frameworks to confirm that CAPA actions and process improvements produce measurable, sustained outcomes - not just short-term fluctuations. * Develop performance attribution ...

Quality Engineer

Portland, OR · On-site

$76K - $98K/yr

Coordinate planning, implementation and trending of multiple quality management systems including CAPA, SCAR, and non-conformances. * Perform internal and supplier audits * Assist in the writing and ...

Quality Engineer 2

Hillsboro, OR · On-site

$78K - $101K/yr

Provide quality support throughout the product lifecycle, including CAPA, Health Hazard Evaluations, risk management, and design changes. * Lead product risk management activities and ensure ...

Quality Engineer 2

Hillsboro, OR · On-site

$78K - $101K/yr

Provide quality support throughout the product lifecycle, including CAPA, Health Hazard Evaluations, risk management, and design changes. * Lead product risk management activities and ensure ...

Senior Quality Engineer

Hillsboro, OR · On-site

$96K - $130K/yr

Provides ongoing quality engineering support throughout the product life cycle, including CAPA investigations, and design changes. * Drives product risk management activities. Ensures identified ...

Implement and support quality assurance and quality control processes, including corrective and preventive action (CAPA) and return material authorization (RMA) procedures. * Investigate quality and ...

Direct and collaborate with supplier representatives on quality problems, ensure that effective corrective actions are implemented (CAPA, SCAR), and contribute to supplier quality improvement ...

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Showing results 1-20

Capa information

See Oregon salary details

$14

$42

$70

How much do capa jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for capa in Oregon is $42.06, according to ZipRecruiter salary data. Most workers in this role earn between $31.89 and $48.91 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of a CAPA specialist?

A CAPA specialist is responsible for investigating quality issues, identifying root causes, and implementing corrective and preventive actions to ensure ongoing compliance and product integrity. Their typical day involves reviewing nonconformance reports, collaborating with cross-functional teams, documenting findings, and tracking the progress of CAPA initiatives using specialized software. CAPA specialists also prepare reports for audits and may facilitate meetings to drive continuous improvement activities. This role often requires balancing multiple projects and deadlines in a regulated environment, making organizational and communication skills crucial for success.

What are the key skills and qualifications needed to thrive in the Capa position, and why are they important?

To thrive as a CAPA (Corrective and Preventive Action) specialist, you need expertise in quality management systems, root cause analysis, and compliance with industry standards, typically backed by a degree in engineering, life sciences, or a related field. Familiarity with CAPA software, regulatory frameworks (such as ISO 13485 or FDA 21 CFR Part 820), and document control systems is essential. Strong analytical thinking, attention to detail, and effective communication skills are vital soft skills for this role. These skills ensure effective problem-solving and sustained compliance, which are essential for maintaining product quality and meeting regulatory requirements.

What is a CAPA job?

A CAPA (Corrective and Preventive Action) job involves identifying, investigating, and resolving quality issues in industries like manufacturing, healthcare, and pharmaceuticals. CAPA professionals analyze root causes of defects or process failures and implement corrective actions to prevent recurrence. They ensure compliance with regulatory standards, document findings, and improve overall quality management systems. Their role is critical in maintaining product safety, efficiency, and regulatory adherence.

What are popular job titles related to Capa jobs in Oregon? For Capa jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Capa jobs in Oregon look for? The top searched job categories for Capa jobs in Oregon are:
Infographic showing various Capa job openings in Oregon as of July 2026, with employment types broken down into 89% Full Time, 4% Part Time, 1% Temporary, 5% Contract, and 1% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $87,484 per year, or $42.1 per hour.
Quality Engineer - CAPA

$98K - $134K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago


Siemens Healthineers rating

8.5

Company rating: 8.5 out of 10

Based on 87 frontline employees who took The Breakroom Quiz

82nd of 486 rated machine equipment manufacturers


Job description

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.
Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.

Siemens Healthineers is seeking a dedicated and detail-oriented Quality Engineer to manage and enhance our Corrective and Preventive Action (CAPA) program and processes. The Quality Engineer will be responsible for overseeing the development, implementation, and maintenance of CAPA processes to ensure compliance with regulatory standards and drive continuous improvement in product quality and operational efficiency. This role requires strong analytical skills, cross-functional collaboration, and expertise in quality management systems (QMS).

You are responsible for:

  • Leading the end-to-end CAPA process, including identification, documentation, investigation, root cause analysis, corrective/preventive action planning, implementation, and effectiveness verification.

  • Facilitating cross-functional CAPA board meetings, documenting minutes, and following up on action items.

  • Designing, implementing, and maintaining CAPA processes in alignment with ISO 13485, MDSAP, FDA regulations, and company policies.

  • Utilizing quality tools (e.g., 5 Whys, Fishbone Diagrams, FMEA) to identify root causes of non-conformances and implement effective solutions.

  • Ensuring CAPA documentation meets regulatory and audit requirements while maintaining accurate records in the QMS.

  • Collaborating with engineering, manufacturing, supply chain, and regulatory teams to resolve quality issues and implement CAPA solutions.

  • Training staff on CAPA processes and promoting a culture of quality and continuous improvement.

  • Administering the CAPA software tool, including creating and managing user accounts.

  • Monitoring CAPA metrics, generating reports, and presenting findings to leadership to drive data-driven decisions.

  • Serving as Subject Matter Expert during internal and external audits, supporting backroom and frontroom activities.

  • Conducting internal audits for the Molecular Imaging audit program.

Minimum Qualifications:

  • Bachelor's degree in engineering, Quality Management, or a related field. Advanced degree or certifications (e.g., ASQ CQE, Six Sigma) preferred.

  • Minimum of 2+ years of experience in quality engineering or a related role.

  • Proven experience managing CAPA programs in a regulated industry (e.g., medical devices, aerospace, pharmaceuticals, or manufacturing).

  • Familiarity with quality management systems (e.g., ISO 13485, 21 CFR Part 820).

  • Strong knowledge of CAPA processes, root cause analysis, and quality tools.

  • Excellent problem-solving and analytical skills.

  • Proficiency in QMS software (e.g., CATSweb, MasterControl, TrackWise, or similar).

  • Strong communication and interpersonal skills for cross-functional collaboration.

  • Detail-oriented with a focus on compliance and documentation.

Preferred Qualifications:

  • Experience with regulatory audits and inspections.

  • Knowledge of lean manufacturing or Six Sigma methodologies.

  • Ability to manage multiple CAPA projects simultaneously.

Who we are: We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.

How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual's potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world's most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

To find out more about Siemens Healthineers businesses, please visit our company page here.

The base pay range for this position is:

$98,140 - $134,937

Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.

If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance.

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time.

Equal Employment Opportunity Statement: Siemens Healthineers is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.

EEO is the Law: Applicants and employees are protected under Federal law from discrimination. To learn more, click here.

Reasonable Accommodations: Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that persons with disabilities are provided reasonable accommodations.

If you require a reasonable accommodation in completing a job application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here. If you're unable to complete the form, you can reach out to our HR People Connect People Contact Center for support at peopleconnectvendorsnam.func@siemens-healthineers.com. Please note HR People Connect People Contact Center will not have visibility of your application or interview status.

California Privacy Notice: California residents have the right to receive additional notices about their personal information. To learn more, click here.

Export Control: "A successful candidate must be able to work with controlled technology in accordance with US export control law." "It is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations."

Data Privacy: We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open. Register here to get started.

Beware of Job Scams: Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as Siemens Healthineers recruiters/employees. These scammers may attempt to collect your confidential personal or financial information. If you are concerned that an offer of employment with Siemens Healthineers might be a scam or that the recruiter is not legitimate, please verify by searching for the posting on the Siemens Healthineers career site.

To all recruitment agencies: Siemens Healthineers does not accept agency resumes. Please do not forward resumes to our jobs alias, employees, or any other company location. Siemens Healthineers is not responsible for any fees related to unsolicited resumes.


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