Principal Quality Engineer Visa Sponsorship Jobs in Minnesota
Principal quality engineer visa sponsorship jobs in Minnesota are concentrated in the Twin Cities metro, where companies like Medtronic, 3M, Boston Scientific, and Ecolab maintain large engineering organizations. Medical device and industrial technology firms drive consistent demand for senior QE talent, making Minneapolis-Saint Paul one of the more active markets for sponsored principal quality engineer roles.
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Get Access To All JobsJob Description:
This person must be able to travel 5-10% globally (possibly Sweden, China, Finland, also local.) Approximately 5-10 trips per year.
As a Principal Supplier Engineer, you'll be the bridge between Boston Scientific Cardiac Diagnostics (CDx) cutting-edge design leading the integration of new and existing technologies into CDx's global supply chain.
Your work will directly impact the reliability, scalability, and speed at which life-changing devices reach patients.
As the technical lead, you'll work with R&D, Quality, Operations, and Regulatory team members to integrate OEM and sub-system supplier designs along with supplied components into CDx's products to ensure compliance, performance, and safety requirements are met.
This role has a wide scope of responsibilities ranging from ensuring supplier design assurance, supplier product development integration assurance, and third-party manufacturing assurance.
Responsibilities:
- Working with Medical Device OEM, sub-system and component suppliers to identify supplier specifications with the end goal of successfully integrating supplied designs and components into CDx's development and manufacturing processes.
- Partnering with R&D, Design Assurance, Manufacturing Engineering, Operations Quality, and Project Management to execute supplier control deliverables according to program needs, such as purchased material qualifications, supplier-driven change assessments, supplier design or capability improvement projects, or regulated compliance assessments.
- Generating and reviewing quality plans, agreements, product specifications, component qualifications, design verification/validations, and process validations.
- Investigating complaints and managing supplier investigations for both design and manufacturing-related issues.
- Participating in supplier audits to assess design and manufacturing compliance to regulatory standards and CDx agreed specification requirements. Audit activities include the evaluation of audit observations and findings, reporting, follow-up, and confirmation of follow-up actions.
- Acting as a technical expert to ensure repeatable and reproducible quality/reliability during the life of the product.
Requirements
- Bachelor's degree in engineering or related discipline.
- 7+ years of technical experience working in Medical Device development processes.
- Experience in design controls, risk management, process validation, and CAPA.
- Design Assurance experience.
- Component and supplier qualification experience.
- Strong Project Management skills.
- Auditor of ISO 13485 quality systems (ISO 13485 Certified Auditor preferred).
- Self-driven and results oriented with strong data analytics and critical thinking skills.
- Experience managing projects and working with cross-functional teams to drive deliverables.
- Experience working with suppliers and familiar with the application of design controls and supplier controls as per 21CFR820 and MDR.
- Supplier design assurance, supplier product development integration assurance, and third-party manufacturing assurance.
Job Description:
This person must be able to travel 5-10% globally (possibly Sweden, China, Finland, also local.) Approximately 5-10 trips per year.
As a Principal Supplier Engineer, you'll be the bridge between Boston Scientific Cardiac Diagnostics (CDx) cutting-edge design leading the integration of new and existing technologies into CDx's global supply chain.
Your work will directly impact the reliability, scalability, and speed at which life-changing devices reach patients.
As the technical lead, you'll work with R&D, Quality, Operations, and Regulatory team members to integrate OEM and sub-system supplier designs along with supplied components into CDx's products to ensure compliance, performance, and safety requirements are met.
This role has a wide scope of responsibilities ranging from ensuring supplier design assurance, supplier product development integration assurance, and third-party manufacturing assurance.
Responsibilities:
- Working with Medical Device OEM, sub-system and component suppliers to identify supplier specifications with the end goal of successfully integrating supplied designs and components into CDx's development and manufacturing processes.
- Partnering with R&D, Design Assurance, Manufacturing Engineering, Operations Quality, and Project Management to execute supplier control deliverables according to program needs, such as purchased material qualifications, supplier-driven change assessments, supplier design or capability improvement projects, or regulated compliance assessments.
- Generating and reviewing quality plans, agreements, product specifications, component qualifications, design verification/validations, and process validations.
- Investigating complaints and managing supplier investigations for both design and manufacturing-related issues.
- Participating in supplier audits to assess design and manufacturing compliance to regulatory standards and CDx agreed specification requirements. Audit activities include the evaluation of audit observations and findings, reporting, follow-up, and confirmation of follow-up actions.
- Acting as a technical expert to ensure repeatable and reproducible quality/reliability during the life of the product.
Requirements
- Bachelor's degree in engineering or related discipline.
- 7+ years of technical experience working in Medical Device development processes.
- Experience in design controls, risk management, process validation, and CAPA.
- Design Assurance experience.
- Component and supplier qualification experience.
- Strong Project Management skills.
- Auditor of ISO 13485 quality systems (ISO 13485 Certified Auditor preferred).
- Self-driven and results oriented with strong data analytics and critical thinking skills.
- Experience managing projects and working with cross-functional teams to drive deliverables.
- Experience working with suppliers and familiar with the application of design controls and supplier controls as per 21CFR820 and MDR.
- Supplier design assurance, supplier product development integration assurance, and third-party manufacturing assurance.
Principal Quality Engineer Job Roles in Minnesota
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Search Principal Quality Engineer Jobs in MinnesotaPrincipal Quality Engineer Jobs in Minnesota: Frequently Asked Questions
Which companies in Minnesota sponsor visas for principal quality engineers?
Minnesota's medical device corridor is the strongest source of principal quality engineer sponsorships. Medtronic, Boston Scientific, and St. Jude Medical parent Abbott have all filed Labor Condition Applications for senior engineering roles in this category. Industrial companies like 3M and Ecolab also sponsor at the principal level. These employers operate large regulatory and quality functions that require the seniority and technical depth a principal quality engineer brings.
What visa types realistically apply to principal quality engineer roles in Minnesota?
Principal quality engineer is a specialty occupation requiring at least a bachelor's degree in engineering or a closely related field, so the H-1B visa is the most common path. Canadian and Mexican nationals may qualify under the TN visa as engineers under the USMCA profession list. Singaporean and Chilean nationals can explore the H-1B1 visa. Candidates already on F-1 OPT or STEM OPT may work for a sponsoring employer while a longer-term petition is filed. An EB-2 or EB-3 employment-based green card is the typical permanent residence route.
How to find principal quality engineer visa sponsorship jobs in Minnesota?
Migrate Mate lists Minnesota employers with verified visa sponsorship history for engineering roles, including principal quality engineer positions. Searching by state and role on Migrate Mate surfaces companies that have actively filed for sponsored hires rather than those that only claim to be open to sponsorship. This is particularly useful in Minnesota's medical device sector, where sponsorship activity is concentrated among a core group of large employers in the Twin Cities metro.
Which Minnesota cities have the most principal quality engineer sponsorship jobs?
Minneapolis and its western suburbs, including Plymouth, Fridley, and Arden Hills, account for the large majority of principal quality engineer sponsorship activity in Minnesota. Medtronic's global headquarters is in Dublin but its U.S. operations hub sits in Fridley, while Boston Scientific operates out of Maple Grove. Saint Paul and the broader I-494 corridor also host significant quality engineering headcount. Smaller but active markets include Rochester, home to Mayo Clinic's technology and engineering operations.
Are there state-specific factors that affect principal quality engineer sponsorship in Minnesota?
Minnesota's concentration of FDA-regulated medical device manufacturers creates persistent demand for principal quality engineers with regulatory affairs and quality management system experience. Roles supporting ISO 13485 or 21 CFR Part 820 compliance are particularly common and tend to require the advanced credentials that justify sponsorship. The University of Minnesota and local engineering programs provide some domestic pipeline, but the specialized intersection of quality engineering and medical device regulation creates ongoing hiring gaps that multinational employers fill through international sponsorship.
What is the prevailing wage for sponsored principal quality engineer jobs in Minnesota?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.