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Capa Engineer Jobs in Minnesota (NOW HIRING)

Senior Manufacturing Engineer

Delano, MN · On-site

$95K - $123K/yr

Apply engineering theory and principles to ensure that the Value Stream for specific products is ... CAPA- Active member of the CAPA team responsible for implementing permanent corrective actions.

Quality Engineer III

Arden Hills, MN · On-site

$72K - $94K/yr

This team is seeking a Quality Engineer III to support the Packaging, Sterilization, and Men ... Support and strengthen quality system processes, including CAPA, investigations and process ...

Quality Engineer

Big Lake, MN

$75K - $96K/yr

Quality Engineer The Quality Engineer develops and improves manufacturing processes and products ... Proven experience working with NCR and CAPA processes from initiation through closure. * Experience ...

Senior Quality Engineer

Minneapolis, MN · On-site

$93K - $131K/yr

... CAPA, complaint investigations, and continuous improvement within a regulated environment ... Provide quality engineering leadership and support for manufacturing, assembly, testing, packaging ...

Quality Engineer III

Arden Hills, MN · On-site

$75K - $97K/yr

This team is seeking a Quality Engineer III to support the Packaging, Sterilization, and Men ... CAPA, investigations and process monitoring activities. ● Apply structured problem-solving ...

Partner with Engineering, Operations, Supply Chain, and customers to ensure products meet ... Lead root cause investigations and CAPA activities to resolve quality issues and strengthen product ...

Quality Engineer III

Arden Hills, MN · On-site

$75K - $97K/yr

This team is seeking a Quality Engineer III to support the Packaging, Sterilization, and Men ... CAPA, investigations and process monitoring activities. • Apply structured problem-solving ...

Quality Engineer

Saint Paul, MN · On-site

$65K - $90K/yr

Complaint & CAPA Management: Manage the full lifecycle of customer complaints from initial receipt ... ASQ Certified Quality Engineer (CQE). * Advanced Quality Tools: Experience with change management ...

Partner with Engineering, Operations, Supply Chain, and customers to ensure products meet ... Lead root cause investigations and CAPA activities to resolve quality issues and strengthen product ...

Quality Engineer II

Minnetonka, MN · On-site

$61 - $123/hr

Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or ... Bachelor's Degree in engineering or Technical Field or an equivalent combination of education and ...

New

Support validations, FMEAs, CAPA activities, and process documentation Must-Have Qualifications: * Manufacturing engineering experience (3-5 years) * Experience in a regulated environment (medical ...

Quality Engineer II

Maple Grove, MN · On-site

$73K - $95K/yr

The Quality Engineer II will provide engineering support at Boston Scientific's Weaver Lake campus ... Lead the implementation of quality assurances, process controls and CAPA systems designed to meet ...

Showing results 41-60

Capa Engineer information

See Minnesota salary details

$38.2K

$99.7K

$134.7K

How much do capa engineer jobs pay per year?

As of Aug 21, 2026, the average yearly pay for capa engineer in Minnesota is $99,657.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,300.00 and $114,100.00 per year, depending on experience, location, and employer.

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 the most commonly searched types of Capa Engineer jobs in Minnesota?

The most popular types of Capa Engineer jobs in Minnesota are:

Infographic showing various Capa Engineer job openings in Minnesota as of August 2026, with employment types broken down into 90% Full Time, 5% Part Time, 4% Contract, and 1% Nights. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $99,657 per year, or $47.9 per hour.

Senior Manufacturing Engineer

Trelleborg

Delano, MN • On-site

$95K - $123K/yr

Full-time

Re-posted 14 days ago


Trelleborg rating

8.2

Company rating: 8.2 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

87th of 543 rated manufacturers


Job description

Trelleborg Medical Solutions is seeking a Senior Manufacturing Engineer to join their team in Delano, MN. Follows good manufacturing practices (GMP) and principles to provide engineering support and develop robust manufacturing processes. Has a primary role in the engineering of new, modified and/or existing manufacturing operations in a clean-room environment. Apply engineering theory and principles to ensure that the Value Stream for specific products is optimized using Lean Sigma tools.
Responsibilities:
  • Analyze product specifications and translate these into manufacturing processes to establish production rates, achieve expected quality levels and establish reliability of finished product.
  • Identifies tooling related issues and communicates/works with a tool maker to resolve the issues
  • Develop manufacturing methods for new and existing products, establish labor standards and develop product cost information.
  • Meticulously document all manufacturing process information and sequences within the Trelleborg document control system.
  • Identify opportunities for improvement to existing processes and methods using data or observation. Develop the improvements and implement them as quickly as practical.
  • Make improvements to production rates and reduce scrap by identifying and implementing new and better equipment, processes or human factors methods.
  • Assist production in troubleshooting production problems with individual components, individual processes and help improve the situation to assure customer delivery dates and superior quality.
  • Review production schedules and engineering specifications to resolve production problems.
  • CAPA- Active member of the CAPA team responsible for implementing permanent corrective actions.
  • DMR- Participate in determination of product DMR disposition plan and approval with the VS team.
  • Follow ISO 13485 and 21 CFR part 11 and part 820 and Trelleborg Quality System protocols.
  • Execution of DOE's, problem solving, FMEA's, validations, control plans, continuation engineering for products.
  • Actively Support Production, Engineering and Quality departments.

Senior Manufacturing Engineer: including all the above
  • Mentors Manufacturing Engineers and Technicians through experiences and education as opportunities arise
  • Develops ideas and strategies to improve operational efficiency, add value, aid business performance and work towards a culture of continuous improvement.
  • Successfully manages multiple high-profile projects simultaneously

Education and Experience Requirements:
  • Bachelor's Degree in Industrial, Manufacturing or Mechanical Engineering or related discipline.
  • Lean Sigma Green or Black Belt certification

  • Polymer Science, Lean Kaizen or other specialized background
  • 7 years of experience in manufacturing engineering or related discipline
  • Demonstrated leadership skills

  • Medical device manufacturing experience

Competencies
  • Ability to read, write, speak and understand the English language
  • Ability to communicate clearly by conveying and receiving ideas, information, and direction effectively
  • Ability to demonstrate adequate job knowledge to deliver a world-class performance
  • Ability to challenge oneself to consistently meet all goals and deadlines
  • Willingness to strive for excellence by producing work that is free of errors and mistakes
  • Desire to delight both customers and coworkers by offering encouragement, fostering teamwork and addressing conflict appropriately
  • Commitment to making improvements company-wide
  • Demonstrated competence using Microsoft Office
  • Use of statistical analysis software
  • Interpersonal skills and good communication technique
  • Ability to coordinate multiple projects and deadlines, manage and identify the scope
  • Act as a project leader on major projects
  • Lean Manufacturing- Proficient in the use of problem-solving tools such as 5 why, Fishbone, 8D, etc.
  • Understanding of manufacturing processes for medical components and devices.
  • Good understanding of metrology principles and methods.

Salary Range $95,000 - $123,000 based on experience
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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