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Remote Capa Engineer Jobs in Minnesota (NOW HIRING)

Protolabs

Quality Systems Engineer

Rosemount, MN · On-site +1

This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our ... Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness ...

Protolabs

Quality Systems Engineer

Maple Plain, MN · On-site +1

This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our ... Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness ...

Protolabs

Quality Systems Engineer

Rosemount, MN · On-site +1

$69K - $92K/yr

This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our ... Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness ...

Protolabs

Quality Systems Engineer

Maple Plain, MN · On-site +1

$69K - $92K/yr

This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our ... Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness ...

Protolabs

Quality Systems Engineer

Plymouth, MN · On-site +1

This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our ... Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness ...

Protolabs

Quality Systems Engineer

Plymouth, MN · On-site +1

$69K - $92K/yr

This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our ... Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness ...

kindeva

Validation Systems Administrator

Woodbury, MN · Remote

Collaborate with Quality, IT, Engineering, and Manufacturing teams to ensure compliant system use ... Support quality processes such as Change Control, CAPA, Deviations, Complaints, and Document ...

kindeva

Validation Systems Administrator

Woodbury, MN · Remote

Collaborate with Quality, IT, Engineering, and Manufacturing teams to ensure compliant system use ... Support quality processes such as Change Control, CAPA, Deviations, Complaints, and Document ...

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Remote Capa Engineer information

What is the difference between Remote Capa Engineer vs Remote Quality Engineer?

AspectRemote Capa EngineerRemote Quality Engineer
CredentialsISO 13485, FDA regulations, Six SigmaISO 9001, Six Sigma, QA certifications
Work EnvironmentMedical device, pharmaceutical, biotech industriesManufacturing, software, product development
Industry UsagePrimarily healthcare and biotech sectorsBroad across manufacturing, tech, and software
Common Search IntentRegulatory compliance, CAPA processes, medical device qualityProduct quality, testing, process improvement

Remote Capa Engineers focus on managing corrective and preventive actions in regulated industries like healthcare, ensuring compliance with standards such as ISO 13485. Remote Quality Engineers work across various sectors to improve product quality through testing and process improvements. While both roles emphasize quality management, the industry focus and specific certifications differ.

What are the key skills and qualifications needed to thrive as a Remote CAPA Engineer, and why are they important?

To thrive as a Remote CAPA (Corrective and Preventive Action) Engineer, you need a solid background in quality engineering, root cause analysis, and regulatory compliance, often supported by a degree in engineering or a related field. Familiarity with quality management systems (such as ISO 13485 or FDA 21 CFR Part 820), CAPA software, and data analysis tools is typically required. Strong attention to detail, problem-solving skills, and effective virtual communication set standout professionals apart. These skills ensure accurate issue resolution, regulatory adherence, and seamless collaboration in distributed work environments.

How does a Remote CAPA Engineer typically collaborate with cross-functional teams to resolve quality issues?

As a Remote CAPA (Corrective and Preventive Action) Engineer, you’ll regularly work with quality assurance, manufacturing, R&D, and regulatory teams to identify, investigate, and resolve quality concerns. Collaboration often involves virtual meetings, sharing documentation, and following up on action items remotely. Effective communication skills and a proactive approach are crucial for driving investigations, ensuring timely implementation of corrective actions, and verifying their effectiveness. Building strong relationships across departments helps streamline issue resolution and fosters a culture of continuous improvement, even in a remote work setting.

What is a Remote CAPA Engineer?

A Remote CAPA (Corrective and Preventive Action) Engineer is a professional responsible for identifying, investigating, and resolving quality issues within an organization, often working from a remote location. They analyze data, implement corrective and preventive measures, and ensure compliance with industry standards and regulations. Their work is crucial in maintaining product quality and safety, as well as continuous improvement in processes. Remote CAPA Engineers utilize digital tools and communication platforms to collaborate with cross-functional teams and document their findings.
What are the most commonly searched types of Capa Engineer jobs in Minnesota? The most popular types of Capa Engineer jobs in Minnesota are:
What are popular job titles related to Remote Capa Engineer jobs in Minnesota? For Remote Capa Engineer jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Remote Capa Engineer jobs in Minnesota look for? The top searched job categories for Remote Capa Engineer jobs in Minnesota are:
Remote Capa Engineer jobs near you
Quality Systems Engineer

Quality Systems Engineer

Protolabs

Rosemount, MN • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted yesterday

Protolabs rating

9.1

Company rating: 9.1 out of 10

Based on 24 frontline employees who took The Breakroom Quiz

1st of 80 rated plastic manufacturers

Job description

Be yourself at Protolabs 
Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. We are an equal opportunity employer, and we are committed to building a diverse team that feels they are valued in the workplace. So do you feel you do not meet every single requirement but still intrigued? We encourage you to still apply! You can help make our company even better. We do not discriminate based on race, color, national origin, sexual orientation, gender, age, mental or physical ability, or any way you represent yourself. We strongly believe diversity makes for more successful teams. 
 
Why Protolabs? 
We are the leaders in digital manufacturing.  We hire doers, makers, and creative thinkers who tackle our roles with an entrepreneurial spirit.  Our culture is centered around meaningful work that brings new and innovative products to market at unprecedented speeds.  We are a diverse team that comes from all walks of life and take pride in our team who is smart, genuine, humble, and passionate about what we do.  It's our people who fuel our creativity and make our culture feel like home. 

Join our team as a Quality Systems Engineer!
This is a fixed hybrid role (onsite Tuesday-Thursyday & remote Mon/Fri) based in one of our Minnesota locations: Plymouth, Rosemount, or Maple Plain. 

Protolabs is seeking a Quality Systems Engineer to help build, scale, and continuously improve our Quality Management System (QMS) as we grow our leadership in digital manufacturing.

This is a high-impact opportunity for an experienced quality professional who thrives in a fast-paced, evolving environment and is excited to drive process improvement, support audits, and strengthen quality systems at scale.

You'll play a key role in ensuring compliance with global standards while partnering across the business to embed quality into day-to-day operations.

What You Will Do
Quality Management System (Core Responsibility)
  • Manage, maintain, and improve the company's QMS in alignment with ISO 9001, ISO 13485, AS9100, and internal procedures
  • Identify gaps or conflicts between SOPs, work instructions, and regulatory requirements-then drive resolution
  • Support and enhance QMS processes to enable scalability during rapid business growth
Corrective Actions & Problem Solving
  • Lead and manage corrective and preventive actions (CAPA) from investigation through effectiveness verification
  • Conduct root cause analysis using structured methodologies (e.g., 5 Whys, Fishbone, 8D)
  • Partner cross-functionally to resolve quality issues and drive sustainable solutions
Audit Management & Compliance
  • Support planning, execution, and follow-up of internal, external, and customer audits
  • Prepare documentation, coordinate audit activities, and ensure timely closure of findings
  • Progress toward independently leading audits and audit programs
Metrics & Continuous Improvement
  • Develop, track, and analyze quality metrics (e.g., CAPA cycle time, audit findings, nonconformances)
  • Use data and trend analysis to assess QMS effectiveness and recommend improvements
  • Drive continuous improvement initiatives across processes and systems
Cross-Functional Collaboration
  • Work closely with internal stakeholders to support quality initiatives and resolve issues
  • Partner with Quality team members and broader engineering/manufacturing teams
  • Contribute to building a proactive, problem-solving quality culture
Additional Details
  • Travel: Occasional (audit-related; primarily local)
  • Schedule: Standard business hours
  • Work Environment: Combination of office and manufacturing floor
What it Takes
  • Bachelor's degree in Engineering, Science, or related field or equivalent experience
  • 7-10+ years of experience working within a Quality Management System
  • Hands-on experience with:
    • ISO 9001, ISO 13485, and/or AS9100
    • CAPA processes and root cause analysis
    • Internal or external audits
  • Strong analytical and problem-solving skills
  • Ability to manage multiple priorities in a fast-paced environment
  • Strong communication skills and cross-functional collaboration experience
  • Self-starter with a proactive, ownership mindset
  • Comfortable working in ambiguity and driving structure where needed
  • Strong systems thinker who can connect process, compliance, and business impact
  • Confident communicator who can influence across teams
What Sets You Apart
  • ASQ Certification (e.g., CQE, Certified Auditor)
  • Experience in manufacturing or regulated industries
  • Experience developing QMS metrics and performing trend analysis
  • Experience scaling or improving quality systems in a growing organization
What's in it for You
  • We offer a competitive total compensation package
  • In addition, we offer competitive benefits including but not limited to:
    • Health Insurance: Traditional OR High Deductible plan
    • Flexible Spending Accounts
    • Health Savings Account (including employer contributions)
    • Dental and Vision
    • Basic and Supplemental Life Insurance
    • Short-Term and Long-Term Disability
  • Paid caregiver leave
  • You will receive PTO + Wellness Hours + Holiday Pay +  Volunteer Hours
  • 401k with company match and immediate vest
  • Employee Stock Purchase Program with a 15% discount
  • And More!
$69,500 - $92,700 a year
Protolabs offers a competitive total rewards package, and compensation mix vary based on position, such as base wage, as well as other earnings including incentives and commissions. Actual pay offered will vary depending on multiple factors which may include, without limitation, job function, work experience, specialized skills, training, education, and certifications. 
Proto Labs maintains ITAR-compliant operations in all of our United States based facilities.  Due to ITAR regulations, this role is only open to U.S. Citizens, lawful permanent residents (green card holders) or foreign nationals granted refugee or asylee status.  Individuals with temporary visas (e.g. E, F-1, H-1, H-2, L, B, J, TN or OPT) are not eligible for hire in this role.
 
Proto Labs, Inc. is an Equal Opportunity Employer
 
Physical Demands:
While performing the essential duties of this job, the employee is regularly required to sit; use a computer keyboard, monitor and mouse, telephone and printer; reach with hands, and arms, talk, see and hear.  The employee is occasionally required to stand, walk, stoop or kneel and must occasionally lift and/or move up to 25 pounds.
Work Environment:
Indoors (A/C); nonsmoking; the majority of this job function is performed in an office setting requiring normal safety precautions. However, there may be job duties that require the employee to spend time in the manufacturing areas exposed to machinery and noise; eye protection occasionally required. Occasionally works in outside weather conditions. Occasionally works near moving mechanical parts and in high, precarious places and is occasionally exposed to wet and/or humid conditions, fumes or airborne particles, toxic or caustic chemicals, risk of electrical shock and vibration. The noise level in the work environment is usually quiet to moderate.
  

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