As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
Principal Quality System Engineer - CAPA
Maple Grove, MN · On-site
$102K - $194K/yr
Create Alert Principal Quality System Engineer - CAPA Onsite Location(s): Maple Grove, MN, US, 55311 Principal Quality System Engineer - CAPA About the role: As a Principal Quality System Engineer ...
Principal Quality System Engineer - CAPA
Maple Grove, MN · On-site
$102K - $194K/yr
Create Alert Principal Quality System Engineer - CAPA Onsite Location(s): Maple Grove, MN, US, 55311 Principal Quality System Engineer - CAPA About the role: As a Principal Quality System Engineer ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
Quality Manager, CAPA Working at Abbott At Abbott, you can do work that matters, grow, and learn ... Life or Engineering Sciences discipline, preferred. * Overall10+ years of experience with 6 years ...
Quality Manager, CAPA Working at Abbott At Abbott, you can do work that matters, grow, and learn ... Life or Engineering Sciences discipline, preferred. * Overall10+ years of experience with 6 years ...
JOB SUMMARY The CAPA & Recall Coordinator is responsible for the administration, coordination, and ... Bachelor\'s degree in Engineering, Life Sciences, Quality, Regulatory Affairs, or related technical ...
JOB SUMMARY The CAPA & Recall Coordinator is responsible for the administration, coordination, and ... Bachelor\'s degree in Engineering, Life Sciences, Quality, Regulatory Affairs, or related technical ...
JOB SUMMARY The CAPA & Recall Coordinator is responsible for the administration, coordination, and ... Bachelor's degree in Engineering, Life Sciences, Quality, Regulatory Affairs, or related technical ...
Quick apply
JOB SUMMARY The CAPA & Recall Coordinator is responsible for the administration, coordination, and ... Bachelor's degree in Engineering, Life Sciences, Quality, Regulatory Affairs, or related technical ...
Quality Manager, CAPA Working at Abbott At Abbott, you can do work that matters, grow, and learn ... Life or Engineering Sciences discipline, preferred. * Overall10+ years of experience with 6 years ...
Quality Manager, CAPA Working at Abbott At Abbott, you can do work that matters, grow, and learn ... Life or Engineering Sciences discipline, preferred. * Overall10+ years of experience with 6 years ...
Bachelor's degree in Engineering, Life Sciences, Quality, Regulatory Affairs, or related technical ... Working knowledge of CAPA methodologies, root cause analysis tools, and effectiveness verification ...
Bachelor's degree in Engineering, Life Sciences, Quality, Regulatory Affairs, or related technical ... Working knowledge of CAPA methodologies, root cause analysis tools, and effectiveness verification ...
Sr. Quality Systems Specialist- CAPA & Recall
Chaska, MN · On-site
$110K - $115K/yr
JOB SUMMARY The CAPA & Recall Coordinator is responsible for the administration, coordination, and ... Bachelor's degree in Engineering, Life Sciences, Quality, Regulatory Affairs, or related technical ...
Sr. Quality Systems Specialist- CAPA & Recall
Chaska, MN · On-site
$110K - $115K/yr
JOB SUMMARY The CAPA & Recall Coordinator is responsible for the administration, coordination, and ... Bachelor's degree in Engineering, Life Sciences, Quality, Regulatory Affairs, or related technical ...
This Principal Design Assurance Engineer on the Field CAPA team will lead cross functional teams to determine actionable root cause and implement effective solutions for high visibility issues ...
This Principal Design Assurance Engineer on the Field CAPA team will lead cross functional teams to determine actionable root cause and implement effective solutions for high visibility issues ...
This Principal Design Assurance Engineer on the Field CAPA team will lead cross functional teams to determine actionable root cause and implement effective solutions for high visibility issues ...
This Principal Design Assurance Engineer on the Field CAPA team will lead cross functional teams to determine actionable root cause and implement effective solutions for high visibility issues ...
This Principal Design Assurance Engineer on the Field CAPA team will lead cross functional teams to determine actionable root cause and implement effective solutions for high visibility issues ...
This Principal Design Assurance Engineer on the Field CAPA team will lead cross functional teams to determine actionable root cause and implement effective solutions for high visibility issues ...
This Principal Design Assurance Engineer on the Field CAPA team will lead cross functional teams to determine actionable root cause and implement effective solutions for high visibility issues ...
This Principal Design Assurance Engineer on the Field CAPA team will lead cross functional teams to determine actionable root cause and implement effective solutions for high visibility issues ...
This Principal Design Assurance Engineer on the Field CAPA team will lead cross functional teams to determine actionable root cause and implement effective solutions for high visibility issues ...
This Principal Design Assurance Engineer on the Field CAPA team will lead cross functional teams to determine actionable root cause and implement effective solutions for high visibility issues ...
Complaints Engineer
Arden Hills, MN · On-site
$75K - $97K/yr
Complaints Engineer - QE / Complaints / CAPA / Post Market Key Responsibilities: • Analyze post-market surveillance data, complaints, and adverse events • Lead root cause investigations and ...
Complaints Engineer
Arden Hills, MN · On-site
$75K - $97K/yr
Complaints Engineer - QE / Complaints / CAPA / Post Market Key Responsibilities: • Analyze post-market surveillance data, complaints, and adverse events • Lead root cause investigations and ...
Senior Quality Engineer - Medical Devices
Arden Hills, MN · On-site
$92K - $125K/yr
Senior Quality Engineer - Medical Devices Location: Arden Hills, MN - Onsite Job Summary: We are ... Support CAPA, NCR, and complaint investigations, including root cause analysis and effectiveness ...
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Senior Quality Engineer - Medical Devices
Arden Hills, MN · On-site
$92K - $125K/yr
Senior Quality Engineer - Medical Devices Location: Arden Hills, MN - Onsite Job Summary: We are ... Support CAPA, NCR, and complaint investigations, including root cause analysis and effectiveness ...
Quality Engineer - Medical Devices
Minneapolis, MN · On-site
$75K - $97K/yr
Northwest Minneapolis Metro Area Type: 6-Month Contract-to-Hire Job Summary Seeking a Quality Assurance Engineer to support quality systems, manufacturing operations, CAPA, validation, audits, and ...
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Quality Engineer - Medical Devices
Minneapolis, MN · On-site
$75K - $97K/yr
Northwest Minneapolis Metro Area Type: 6-Month Contract-to-Hire Job Summary Seeking a Quality Assurance Engineer to support quality systems, manufacturing operations, CAPA, validation, audits, and ...
Quality Engineer
Coon Rapids, MN · On-site
$80K - $100K/yr
NCR and CAPA Management: * Manage NCR, CAPA, and customer complaints from creation to closure ... The Quality Engineer has a functional link with the QAR/QA inspectors. In case of any issue ...
Quality Engineer
Coon Rapids, MN · On-site
$80K - $100K/yr
NCR and CAPA Management: * Manage NCR, CAPA, and customer complaints from creation to closure ... The Quality Engineer has a functional link with the QAR/QA inspectors. In case of any issue ...
Capa Engineer information
See Minnesota salary details
$38.2K - $47K
3% of jobs
$47K - $55.7K
3% of jobs
$55.7K - $64.5K
4% of jobs
$64.5K - $73.3K
7% of jobs
$73.3K - $82K
6% of jobs
$82.8K is the 25th percentile. Wages below this are outliers.
$82K - $90.8K
6% of jobs
The median wage is $98.7K / yr.
$90.8K - $99.6K
21% of jobs
$99.6K - $108.4K
4% of jobs
$114K is the 75th percentile. Wages above this are outliers.
$108.4K - $117.1K
29% of jobs
$117.1K - $125.9K
2% of jobs
$125.9K - $134.7K
13% of jobs
$38.2K
$99.7K
$134.7K
How much do capa engineer jobs pay per year?
What is a CAPA engineer?
A CAPA (Corrective and Preventive Action) Engineer is responsible for identifying, investigating, and resolving quality issues in manufacturing or engineering processes. They analyze root causes of defects, implement corrective measures, and develop preventive strategies to ensure compliance with industry regulations. CAPA Engineers work closely with cross-functional teams to improve product quality, streamline processes, and maintain regulatory compliance. They also document findings, track action plans, and support continuous improvement initiatives to reduce future risks.
What are the main daily responsibilities of a CAPA engineer?
A CAPA Engineer's daily responsibilities typically include investigating potential or actual nonconformities, conducting root cause analyses, and developing corrective and preventive action plans to resolve and prevent future issues. They also collaborate closely with cross-functional teams such as manufacturing, quality assurance, and regulatory affairs to ensure solutions are practical and compliant with industry standards. Additionally, CAPA Engineers monitor the progress and effectiveness of implemented actions, prepare documentation for audits, and participate in continuous process improvement initiatives. This role is crucial for maintaining the highest quality standards and ensuring compliance in regulated industries such as medical devices or pharmaceuticals.
What are the key skills and qualifications needed to thrive in the CAPA engineer position, and why are they important?
To thrive as a CAPA Engineer, you need a solid background in quality engineering, root cause analysis, and process improvement, typically supported by a degree in engineering or a related technical field. Familiarity with CAPA management systems, quality standards such as ISO 13485 or ISO 9001, and tools like Six Sigma or FMEA is highly valuable. Strong problem-solving abilities, attention to detail, and effective communication skills distinguish top performers in this role. These competencies ensure effective identification, documentation, and resolution of quality issues, helping organizations maintain regulatory compliance and deliver high-quality products.
What are popular job titles related to Capa Engineer jobs in Minnesota?
For Capa Engineer jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Capa Engineer jobs in Minnesota look for?
The top searched job categories for Capa Engineer jobs in Minnesota are:

Principal Quality System Engineer - CAPA
Maple Grove, MN • Hybrid
Full-time
Posted 16 days ago
Boston Scientific rating
8.5
Based on 120 frontline employees who took The Breakroom Quiz
Job description
Recruiter: Spencer Gregory Hale
Principal Quality System Engineer - CAPA
About the role:
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective and Preventive Action (CAPA) process across the Maple Grove site.
The Principal Quality Systems Engineer will be the Technical Leader representing the CAPA process to internal and external stakeholders. This includes CAPA Investigations, Product/Material/System Nonconformances, and Field Action support. This role partners closely with Site Leadership, Maple Grove CAPA team members, investigation owners, as well as Regional and Global Quality Systems personnel. They will provide mentorship to Quality team members and cross-functional stakeholders to enable high-quality investigations, robust root cause identification, and sustainable corrective and preventive actions.
Work model, sponsorship, relocation:
At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time.
Your responsibilities will include:
- Partner with Site Leadership to maintain and improve CAPA process, tools, and governance models
- Act as a Subject Matter Expert (SME) for the CAPA process, providing guidance on expectations, requirements, and best practices
- Monitor Nonconformance and CAPA performance metrics (e.g., timeliness, effectiveness, aging) and identify trends, gaps, and improvement opportunities
- Support development and distribution of Nonconformance and CAPA metrics for management review and quality forums
- Provide guidance on nonconformance investigations to support appropriate scoping, risk assessments, corrections, and material/product containment (including physical segregation/identification).
- Provide guidance to CAPA owners and cross-functional teams on root cause analysis and solution development
- Provide mentorship for Site CAPAs
- Build organizational capability in Nonconformance and CAPA execution by supporting development and deployment of training and tools
- Partner with cross-functional stakeholders to drive standardization and adoption of best practices across sites
- Drive continuous improvement and efficiencies to support a preventive quality culture
- Support internal and external audits and inspections by providing Nonconformance and CAPA related documentation and subject matter expertise
- Act as a Quality System resource for external audit readiness, including field action support
Qualifications:
Required qualifications:
- Bachelor's degree
- Minimum of 7 years' experience in the medical device or pharmaceutical industry
- Minimum of 5 years' experience in a Quality role that includes Nonconformance/CAPA support
- Direct experience executing, supporting, or mentoring complex CAPAs
- Practical understanding of nonconformance regulatory requirements and best practices, including material identification, labeling, and segregation
- In-depth knowledge of regulations/standards such as 21 CFR 820 and ISO 13485
- Experience supporting audits or regulatory inspections
- Experience leading or supporting cross-functional initiatives or projects
- Strong problem-solving and root cause analysis skills
- Strong communication and stakeholder management skills
- Ability to make sound, risk-based decisions
Preferred qualifications:
- Strong interpersonal skills with the ability to collaborate effectively across Quality, Manufacturing, Engineering, Regulatory, and Supply Chain functions
- Ability to clearly document and communicate investigation outcomes and recommendations to technical and non-technical stakeholders
- High attention to detail, organizational skills, and a disciplined approach to compliance and documentation
- Proactive problem solver with a continuous improvement mindset
- Ability to manage priorities in a fast-paced environment with strict regulatory timelines
Requisition ID: 633661
Minimum Salary: $ 102100
Maximum Salary: $ 194000
The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.
Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).
Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).
For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.
What Boston Scientific employees say
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About Boston Scientific
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As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen.
Industry
Medical equipment and supplies manufacturing, manufacturing and construction
Company size
10,000+ Employees
Headquarters location
Marlborough, MA, US