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Capa Engineer Jobs in Minnesota (NOW HIRING)

Actalent

Quality Engineer

Saint Paul, MN · On-site

$72K - $94K/yr

Perform thorough root cause analysis on quality issues and develop robust corrective and preventive action (CAPA) plans. * Collaborate with cross-functional teams in engineering, manufacturing, and ...

Abbott

Quality Engineer II

Minnetonka, MN · On-site

$73K - $94K/yr

Quality Engineer II Working at Abbott At Abbott, you can do work that matters, grow, and learn ... Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or ...

Trelleborg

Manufacturing Engineer

Delano, MN · On-site

$75K - $95K/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.

Trelleborg

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.

Boston Scientific

Quality Engineer III

Arden Hills, MN

$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 ...

Trelleborg

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.

Boston Scientific

Quality Engineer III

Arden Hills, MN

$75K - $97K/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 ...

Tactile Medical

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 ...

Actalent

Senior Quality Engineer

Saint Paul, MN · On-site

$89K - $121K/yr

Perform thorough root cause analysis on quality issues and develop robust corrective and preventive action (CAPA) plans. * Collaborate with cross-functional teams in engineering, manufacturing, and ...

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Showing results 41-60

All JobsCapa Engineer JobsCapa Engineer Jobs in Minnesota

Capa Engineer information

See Minnesota salary details

$38.2K

$99.7K

$134.7K

How much do capa engineer jobs pay per year?

As of Sep 11, 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 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:

Capa Engineer jobs near you
Infographic showing various Capa Engineer job openings in Minnesota as of August 2026, with employment types broken down into 91% Full Time, 2% Part Time, and 7% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $99,657 per year, or $47.9 per hour.

Lab Quality Engineer III - Arden Hills, Minnesota - (on-site)

Arden Hills, MN • On-site

Verito Solutions
See more jobs at Verito Solutionsexternal

$75K - $97K/yr

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Position:  Lab Quality Engineer III
Location: Arden Hills, Minnesota - (on-site)
Contract: 12+ months
 

Job Description:

The Preclinical Laboratory Quality Engineer provides quality support for 
Preclinical testing laboratories, suppliers and studies worldwide to determine compliance
with established internal and external requirements, including ISO 13485, 21 CFR 820, 21
CFR 58, ISO 10993 and ISO/IEC 17025, as applicable. This role evaluates quality system
effectiveness, supports inspection readiness and contributes to the Preclinical Corrective
and Preventive Action (CAPA) program.
This position serves as Quality Assurance or Quality Engineer, as applicable, for internal 

procedures and preclinical laboratory studies, and conducts internal and
external quality reviews to ensure compliance with regulatory requirements and company
policies.
Responsibilities will include:
• Support laboratory functions to maintain compliance with applicable regulations
and standards, validated methods, and internal policies, procedures and work
instructions, while promoting continuous inspection readiness.
• Collaborate with quality management and laboratory management on process
improvement initiatives, quality trends and continuous improvement projects.
• Conduct internal and external quality assurance audits of systems, testing
laboratories, procedures and controls used in testing activities under applicable
regulations and standards.
• Plan, schedule and conduct vendor audits.
• Partner with global preclinical teams and Strategic Sourcing regarding new vendor
requests and ongoing vendor needs.
• Evaluate the adequacy and compliance of systems, operations and practices
through facility- and process-based audits and quality monitoring activities.
• Assess the accuracy, validity and overall quality of preclinical study data.
• Communicate final results of quality reviews and audits to management and
technical staff.
• Write and publish audit and quality review reports, obtain appropriate approvals and
distribute findings to responsible stakeholders.
• Oversee follow-up of corrections and corrective actions, escalate overdue items
and support timely closure.
• Support or lead assigned quality projects and initiatives.
• Track audits and responses, support document review activities and maintain
appropriate records.
• Contribute to the development and continuous improvement of quality procedures
and processes.
• Assist laboratories in preparation for accrediting body, notified body, FDA or other
regulatory inspections.
• Support the preclinical organization in meeting  Quality System
requirements.
• Support the CAPA process in partnership with CAPA owners.
• Support compliance review meetings in accordance with site procedures.
Qualifications:
Required qualifications:
• Bachelor’s degree in chemistry or related life sciences discipline
• Strong technical and quality knowledge of ISO/IEC 17025, ISO 13485 and/or 21 CFR 58
• Strong verbal and written communication skills, both technical and conversational
• Minimum of 3 years' experience in a technical role
Preferred qualifications:
• Minimum of 2 years' experience working in a quality role
• Minimum of 4--5 years' experience working in the medical device industry or other
similarly regulated industry, such as pharmaceuticals, biologics or preclinical
environments
• Strong experience with 21 CFR 58 (GLP)

Manoj Prajapati | Non-IT Recruiter

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