Quality Assurance Manager Jobs in Minnesota
Quality Assurance Manager jobs in Minnesota are concentrated in the Twin Cities metro, Rochester, and Duluth, where manufacturing, medical device production, and food processing drive steady demand for experienced quality leaders at coordinator through director level. Employers like Medtronic, General Mills, and 3M maintain large quality functions in Minnesota and recruit regularly for managers who can oversee compliance programs, lead audit cycles, and drive continuous improvement initiatives. The most in-demand specialties are medical device quality systems, food safety and regulatory compliance, and ISO-based manufacturing quality. See the openings below and apply to the ones that match your experience.
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Showing 5 of 73+ Quality Assurance Manager jobs
Company Overview
Biomerics is a world-class manufacturer and innovative polymer solutions provider for the medical device and biotech indus-tries. As a vertically integrated company, we specialize in designing, developing, and producing medical devices for diagnostic and interventional procedures. We are focused on next-genera-tion solutions for vascular access, electrophysiology, cardiac rhythm management, neurovascular, structural heart, and cardiovascular markets.
At Biomerics, we are dedicated to our diverse employee base. We understand that a strong, skilled, and engaged workforce is the foundation of our continued success as a business. We strive to live up to Biomerics' values in all our interactions. It is an exciting time to be part of our collective team, and there is no limit to the impact that can be achieved here at Biomerics. We improve and advance the lives of our employees and the patients who depend on our products.
At Biomerics, we believe in integrity, partnership, empowerment and accountability, trust, agility, teamwork, and excellence, and we care. Our team-oriented, customer-focused corporate culture prioritizes building strategic, mutually beneficial partnerships with customers and our team members.
Job Description
The Design Assurance Quality Engineer provides Quality Engineering support for new product development (NPD) projects from concept through design transfer and commercialization, while also supporting sustaining engineering activities for existing products throughout their lifecycle. This position partners with Design Engineering, Manufacturing Engineering, Operations, Supplier Quality, Business Development, and Quality to ensure customer, quality, and regulatory requirements are appropriately incorporated throughout product development and ongoing product support.
The Design Assurance Quality Engineer supports design controls, risk management, verification and validation, supplier and material qualification, design transfer, and product/process change activities in accordance with the Quality Management System (QMS) and applicable regulatory requirements. This position reports to the Site Quality Manager.
Responsibilities
- Execute design, development, and validation activities throughout the product life cycle in accordance with project scope.
- Utilize the Design Control process to create cost-effective and efficiently manufacturable products.
- Contribute to deliverables in compliance with MDR, ISO, and EN standards.
- Translate customer specifications and requirements into clear, concise performance and functional requirements.
- Conduct engineering evaluations, characterizations, design of experiments (DOE), bench testing, and other verification activities to improve and confirm design and process capabilities.
- Train and guide development technicians/operators in hands-on prototyping, testing, and process development.
- Execute document change requests and effectively train development/production operators and technicians on updated documentation.
- Design, procure, install, qualify, document, and train on new tooling/fixturing.
- Evaluate and implement new technologies and ideas for product improvement.
- Use statistical tools to analyze data and make development decisions to enhance process capability.
- Develop and refine manufacturing procedures and test/inspection plans to ensure quality requirements are met and manufacturing process risks are mitigated.
- Bachelor’s degree or technical degree in Engineering or a related technical field; equivalent education and experience may be considered.
- Minimum of 5 years of experience in a medical device manufacturing, product development, Quality Engineering, or related regulated environment.
- Working knowledge of applicable FDA Quality System requirements, ISO 13485, and ISO 14971.
- Experience with medical device design controls and new product development processes.
- Experience with product and process verification and validation activities, including protocol development and execution.
- Experience with DFMEAs, PFMEAs, and Risk Management activities.
- Understanding of design transfer, manufacturing processes, production readiness, and sustaining engineering activities.
- Strong project management and organizational skills with demonstrated initiative in taking ownership of and completing assigned projects.
- Strong verbal and written communication skills, including the ability to effectively document technical and quality activities.
- Ability to work effectively within cross-functional project teams.
- Ability to manage and prioritize multiple projects, objectives, and deadlines in a fast-paced environment.
- Strong analytical and problem-solving skills with attention to detail.
Biomerics offers the following benefits: Medical/Dental/Vision Insurance, Short-Term Disability, Long-Term Disability, Life Insurance, Paid Vacation Days, Paid Holidays, and 401k.
Please, No Recruitment Agency calls or emails (we are not using recruitment services for this or any other role posted).
The salary estimates are estimates from this job board and not a guarantee of Biomerics’ salary range.
Company Overview
Biomerics is a world-class manufacturer and innovative polymer solutions provider for the medical device and biotech indus-tries. As a vertically integrated company, we specialize in designing, developing, and producing medical devices for diagnostic and interventional procedures. We are focused on next-genera-tion solutions for vascular access, electrophysiology, cardiac rhythm management, neurovascular, structural heart, and cardiovascular markets.
At Biomerics, we are dedicated to our diverse employee base. We understand that a strong, skilled, and engaged workforce is the foundation of our continued success as a business. We strive to live up to Biomerics' values in all our interactions. It is an exciting time to be part of our collective team, and there is no limit to the impact that can be achieved here at Biomerics. We improve and advance the lives of our employees and the patients who depend on our products.
At Biomerics, we believe in integrity, partnership, empowerment and accountability, trust, agility, teamwork, and excellence, and we care. Our team-oriented, customer-focused corporate culture prioritizes building strategic, mutually beneficial partnerships with customers and our team members.
Job Description
The Design Assurance Quality Engineer provides Quality Engineering support for new product development (NPD) projects from concept through design transfer and commercialization, while also supporting sustaining engineering activities for existing products throughout their lifecycle. This position partners with Design Engineering, Manufacturing Engineering, Operations, Supplier Quality, Business Development, and Quality to ensure customer, quality, and regulatory requirements are appropriately incorporated throughout product development and ongoing product support.
The Design Assurance Quality Engineer supports design controls, risk management, verification and validation, supplier and material qualification, design transfer, and product/process change activities in accordance with the Quality Management System (QMS) and applicable regulatory requirements. This position reports to the Site Quality Manager.
Responsibilities
- Execute design, development, and validation activities throughout the product life cycle in accordance with project scope.
- Utilize the Design Control process to create cost-effective and efficiently manufacturable products.
- Contribute to deliverables in compliance with MDR, ISO, and EN standards.
- Translate customer specifications and requirements into clear, concise performance and functional requirements.
- Conduct engineering evaluations, characterizations, design of experiments (DOE), bench testing, and other verification activities to improve and confirm design and process capabilities.
- Train and guide development technicians/operators in hands-on prototyping, testing, and process development.
- Execute document change requests and effectively train development/production operators and technicians on updated documentation.
- Design, procure, install, qualify, document, and train on new tooling/fixturing.
- Evaluate and implement new technologies and ideas for product improvement.
- Use statistical tools to analyze data and make development decisions to enhance process capability.
- Develop and refine manufacturing procedures and test/inspection plans to ensure quality requirements are met and manufacturing process risks are mitigated.
- Bachelor’s degree or technical degree in Engineering or a related technical field; equivalent education and experience may be considered.
- Minimum of 5 years of experience in a medical device manufacturing, product development, Quality Engineering, or related regulated environment.
- Working knowledge of applicable FDA Quality System requirements, ISO 13485, and ISO 14971.
- Experience with medical device design controls and new product development processes.
- Experience with product and process verification and validation activities, including protocol development and execution.
- Experience with DFMEAs, PFMEAs, and Risk Management activities.
- Understanding of design transfer, manufacturing processes, production readiness, and sustaining engineering activities.
- Strong project management and organizational skills with demonstrated initiative in taking ownership of and completing assigned projects.
- Strong verbal and written communication skills, including the ability to effectively document technical and quality activities.
- Ability to work effectively within cross-functional project teams.
- Ability to manage and prioritize multiple projects, objectives, and deadlines in a fast-paced environment.
- Strong analytical and problem-solving skills with attention to detail.
Biomerics offers the following benefits: Medical/Dental/Vision Insurance, Short-Term Disability, Long-Term Disability, Life Insurance, Paid Vacation Days, Paid Holidays, and 401k.
Please, No Recruitment Agency calls or emails (we are not using recruitment services for this or any other role posted).
The salary estimates are estimates from this job board and not a guarantee of Biomerics’ salary range.
See All 73 Quality Assurance Manager Jobs in Minnesota
Find roles in Minnesota that match your experience and apply in just a few clicks.
Find JobsQuality Assurance Manager Jobs by City in Minnesota
Where Minnesota roles are concentrated, by current openings.
Quality Assurance Manager Job Market in Minnesota
A snapshot from current Minnesota openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Manufacturing
- Staffing & Recruiting
- Healthcare & Medical Services
- Technology & Software
- Consulting & Professional Services
What Minnesota Employers Look For
The qualifications that appear most often in quality assurance manager jobs across Minnesota.
- Bachelor's degree in engineering, science, or a related technical field required
- Five or more years of quality assurance experience in a regulated Minnesota industry
- Working knowledge of ISO 9001, ISO 13485, or FDA quality system regulations
- Demonstrated experience leading internal audits and managing corrective action processes
- ASQ Certified Quality Manager or Certified Quality Engineer credential strongly preferred
- Proficiency with quality management software and statistical process control tools
Quality Assurance Manager Jobs in Minnesota: Frequently Asked Questions
How do you become a quality assurance manager in Minnesota?
Most quality assurance managers in Minnesota start with a bachelor's degree in engineering, life sciences, or a technical discipline, then build several years of hands-on quality experience in a regulated industry such as medical devices, food manufacturing, or aerospace. Minnesota does not require a state-issued license for this role, but earning an ASQ certification, such as the Certified Quality Manager or Certified Quality Engineer designation, is a recognized credential that Minnesota employers treat as a strong qualifier for management-level positions.
How much do quality assurance managers make in Minnesota?
Quality assurance managers in Minnesota earn a median of about $123,580 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $79,020 for the lowest 10% to over $218,510 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire quality assurance managers in Minnesota?
Minnesota quality assurance manager roles are posted by Cirrus Aircraft, Beckman Coulter Diagnostics, and RION and others right now, based on current listings on Migrate Mate as of September 2026. Minnesota's concentration of medical device manufacturers, Fortune 500 food companies, and advanced manufacturing operations means quality management roles appear across a broad range of established employers in the state.
Which Minnesota cities have the most quality assurance manager jobs?
Chaska, Duluth, and Saint Paul are the cities with the most quality assurance manager openings in Minnesota. The Twin Cities metro drives the largest share of listings because it anchors Minnesota's medical device corridor and is home to major food, technology, and industrial manufacturers, while Rochester's concentration of healthcare and precision manufacturing employers makes it a secondary hub for quality roles.
Are there remote quality assurance manager jobs in Minnesota?
Yes, but they're rare. Quality assurance managers often need to be on the production floor, in the lab, or present during audits, which limits full remote work in most industries. About 17% of quality assurance manager openings tied to Minnesota are remote or hybrid as of September 2026, with the remote portion concentrated in roles focused on documentation, supplier quality management, and quality systems oversight rather than direct production oversight.
How can I get hired as a quality assurance manager in Minnesota with little or no experience?
The most realistic entry path is moving into a quality assurance specialist or quality technician role at a Minnesota manufacturer or medical device company, then progressing internally. Large Minnesota employers in the medical device and food sectors regularly hire quality coordinators and junior auditors from adjacent backgrounds in operations, lab work, or regulatory affairs. Earning an ASQ entry-level certification and gaining familiarity with ISO or FDA documentation standards gives candidates a concrete edge, and community and technical colleges across the Twin Cities offer quality and manufacturing technology programs that provide a practical foundation.
Where can I find and apply to quality assurance manager jobs in Minnesota?
You can find and apply to quality assurance manager jobs in Minnesota on Migrate Mate, which lists current openings across the state. Search the listings, identify the roles that fit your background and industry focus, and apply directly to the ones that match your experience.
See All 73 Quality Assurance Manager Jobs in Minnesota
Find roles in Minnesota that match your experience and apply in just a few clicks.
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