Quality Engineer - CAPA
$98K - $134K/yr
Leading the end-to-end CAPA process, including identification, documentation, investigation, root cause analysis, corrective/preventive action planning, implementation, and effectiveness verification.
$98K - $134K/yr
Leading the end-to-end CAPA process, including identification, documentation, investigation, root cause analysis, corrective/preventive action planning, implementation, and effectiveness verification.
$98K - $134K/yr
Leading the end-to-end CAPA process, including identification, documentation, investigation, root cause analysis, corrective/preventive action planning, implementation, and effectiveness verification.
Salem, OR · On-site
Drive supplier root cause analysis, CAPA, and containment actions for electrical, mechanical, and mixed-technology failures. * Establish and maintain supplier quality requirements, including ...
Salem, OR · On-site
Drive supplier root cause analysis, CAPA, and containment actions for electrical, mechanical, and mixed-technology failures. * Establish and maintain supplier quality requirements, including ...
Drive supplier root cause analysis, CAPA, and containment actions for electrical, mechanical, and mixed-technology failures. * Establish and maintain supplier quality requirements, including ...
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Drive supplier root cause analysis, CAPA, and containment actions for electrical, mechanical, and mixed-technology failures. * Establish and maintain supplier quality requirements, including ...
Drive supplier root cause analysis, CAPA, and containment actions for electrical, mechanical, and mixed-technology failures. * Establish and maintain supplier quality requirements, including ...
Drive supplier root cause analysis, CAPA, and containment actions for electrical, mechanical, and mixed-technology failures. * Establish and maintain supplier quality requirements, including ...
$135K - $225K/yr
Drive root cause analysis for systemic failures using structured problem-solving tools (8D, CAPA, FRACAS) and ensure corrective actions are embedded into design and process standards. * Own and ...
$135K - $225K/yr
Drive root cause analysis for systemic failures using structured problem-solving tools (8D, CAPA, FRACAS) and ensure corrective actions are embedded into design and process standards. * Own and ...
Portland, OR · On-site
Build success validation frameworks to confirm that CAPA actions and process improvements produce measurable, sustained outcomes - not just short-term fluctuations. * Develop performance attribution ...
Portland, OR · On-site
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 ...
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 ...
... CAPA) and continuous improvement initiatives Coordinate proficiency testing programs, reporting, and follow up actions Prepare regulatory and client reports including audit responses and analytical ...
... CAPA) and continuous improvement initiatives Coordinate proficiency testing programs, reporting, and follow up actions Prepare regulatory and client reports including audit responses and analytical ...
Beaverton, OR · On-site
$135K - $225K/yr
Drive root cause analysis for systemic failures using structured problem-solving tools (8D, CAPA, FRACAS) and ensure corrective actions are embedded into design and process standards. * Own and ...
Beaverton, OR · On-site
$135K - $225K/yr
Drive root cause analysis for systemic failures using structured problem-solving tools (8D, CAPA, FRACAS) and ensure corrective actions are embedded into design and process standards. * Own and ...
... CAPA) and continuous improvement initiatives Coordinate proficiency testing programs, reporting, and follow up actions Prepare regulatory and client reports including audit responses and analytical ...
... CAPA) and continuous improvement initiatives Coordinate proficiency testing programs, reporting, and follow up actions Prepare regulatory and client reports including audit responses and analytical ...
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 ...
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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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Happy Valley, OR · On-site
Implement and support quality assurance and quality control processes, including corrective and preventive action (CAPA) and return material authorization (RMA) procedures. * Investigate quality and ...
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Happy Valley, OR · On-site
Implement and support quality assurance and quality control processes, including corrective and preventive action (CAPA) and return material authorization (RMA) procedures. * Investigate quality and ...
Strong knowledge of quality systems and tools including PPAP, FAI, CAPA, 8D, FMEA, control plans, and SPC * Advanced proficiency in GD&T and its application in design, inspection, and supplier ...
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Strong knowledge of quality systems and tools including PPAP, FAI, CAPA, 8D, FMEA, control plans, and SPC * Advanced proficiency in GD&T and its application in design, inspection, and supplier ...
$101K - $152K/yr
Direct and collaborate with supplier representatives on quality problems, ensure that effective corrective actions are implemented (CAPA, SCAR), and contribute to supplier quality improvement ...
$101K - $152K/yr
Direct and collaborate with supplier representatives on quality problems, ensure that effective corrective actions are implemented (CAPA, SCAR), and contribute to supplier quality improvement ...
Strong knowledge of quality systems and tools including PPAP, FAI, CAPA, 8D, FMEA, control plans, and SPC * Advanced proficiency in GD&T and its application in design, inspection, and supplier ...
Strong knowledge of quality systems and tools including PPAP, FAI, CAPA, 8D, FMEA, control plans, and SPC * Advanced proficiency in GD&T and its application in design, inspection, and supplier ...
Manages corrective and preventive actions (CAPA) * Supports internal audits, client audits and regulatory inspections, with the potential to host * Manages controlled document issuance and archival
Manages corrective and preventive actions (CAPA) * Supports internal audits, client audits and regulatory inspections, with the potential to host * Manages controlled document issuance and archival
$14.87 - $19.90
0% of jobs
$19.90 - $24.94
6% of jobs
$24.94 - $29.97
11% of jobs
$31.96 is the 25th percentile. Wages below this are outliers.
$29.97 - $35.01
20% of jobs
The median wage is $39.32 / hr.
$35.01 - $40.04
15% of jobs
$40.04 - $45.08
15% of jobs
$47.59 is the 75th percentile. Wages above this are outliers.
$45.08 - $50.11
16% of jobs
$50.11 - $55.15
9% of jobs
$55.15 - $60.18
4% of jobs
$60.18 - $65.22
2% of jobs
$65.22 - $70.25
2% of jobs
$14
$42
$70
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.
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.
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.

$98K - $134K/yr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 22 days ago
8.5
Based on 87 frontline employees who took The Breakroom Quiz
82nd of 486 rated machine equipment manufacturers
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 - $134,937Factors 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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