Medical Devices TN Sponsorship Jobs in Wisconsin
TN visa sponsorship jobs in Wisconsin's medical devices sector are concentrated around companies like Exact Sciences, Integra LifeSciences, and Spectrum Brands Health, with major hiring in Madison and the Milwaukee metro. Wisconsin's manufacturing depth and growing med-tech presence make it a consistent source of TN-eligible roles for Canadian and Mexican professionals in engineering, quality, and regulatory functions.
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Get Access To All JobsINTRODUCTION
FOR MORE THAN 80 YEARS, Natus has been working in collaboration with clinicians to deliver industry-leading neuro solutions that help providers more easily make sense of the body’s signals. Engineered with input from those who have lived the care experience, our technology simplifies complex processes and improves accuracy and efficiency. There is a role for everyone who wants to be part of the innovative solutions at Natus Neuro.
Location: Middleton, WI (Hybrid Role)
ABOUT THE ROLE
We're looking for an experienced Supplier Quality Engineer to help ensure the quality and reliability of the parts, materials, and services that go into our products. In this role, you'll take ownership of supplier quality activities, working directly with suppliers and internal teams to resolve quality issues, improve supplier performance, and maintain compliance with regulatory requirements. You'll be involved in everything from supplier qualification and audits to investigating complex quality issues and supporting new product introductions. This is an opportunity for someone who enjoys problem-solving, working across different teams, and taking responsibility for driving quality improvements.
Manage Supplier Quality & Performance:
- Take ownership of quality activities for an assigned portfolio of suppliers, ensuring compliance with Natus requirements and applicable regulatory standards.
- Qualify and assess suppliers to ensure they meet established quality expectations.
- Monitor supplier performance, identify trends, and work with suppliers to drive improvements.
- Review and assess supplier change notifications to evaluate potential quality impacts.
Investigate Issues & Drive Solutions:
- Lead investigations into supplier-related nonconformances and manage Supplier Corrective Action Requests (SCARs) through resolution.
- Work closely with suppliers to identify root causes, implement corrective actions, and address recurring quality issues.
- Collaborate with Manufacturing, Engineering, Sourcing, Regulatory Affairs, and other teams to resolve supplier challenges and support business needs.
Lead Supplier Audits & Maintain Compliance:
- Plan, schedule, and conduct supplier quality audits to assess compliance with applicable quality and regulatory requirements.
- Prepare audit reports, communicate findings, and work with suppliers to ensure timely closure of identified issues.
- Support regulatory inspections, including FDA and BSI inspections.
Support Projects & Continuous Improvement:
- Support supplier quality activities related to new product introductions, product transfers, and manufacturing changes.
- Identify opportunities to improve supplier quality processes and performance.
- Independently manage assigned activities and projects, delivering against agreed timelines.
- Contribute to a team culture built on accountability, collaboration, continuous improvement, and patient safety.
WHAT WE'RE LOOKING FOR
We're looking for someone with solid supplier quality experience who is comfortable managing their own priorities, working directly with suppliers, and navigating quality challenges in a regulated environment.
REQUIRED EXPERIENCE & QUALIFICATIONS
- Bachelor's degree and a minimum of 5 years of relevant experience in Quality Engineering, Supplier Quality, or Quality Assurance within the medical device industry or another regulated environment.
- Demonstrated experience independently managing supplier qualifications, audits, nonconformance investigations, and corrective actions.
- Strong working knowledge of ISO 13485, FDA quality system requirements, and applicable medical device regulations.
- Qualified ISO 13485 Lead Auditor with experience conducting supplier audits.
- Experience collaborating with Engineering, Manufacturing, Sourcing, and Quality teams.
- Strong communication, organizational, and problem-solving skills.
- Ability to work independently, manage competing priorities, and follow issues through to resolution.
- Willingness and availability to travel to supplier locations within the US.
NICE TO HAVE
- Experience reviewing and approving supplier validation protocols (IQ/OQ/PQ).
- Experience with First Article Inspections (FAI).
INTERESTED IN JOINING NATUS?
If you have experience in supplier quality, enjoy working through complex quality challenges, and want to contribute to maintaining high standards in medical device manufacturing, we'd like to hear from you.
PAY TRANSPARENCY:
Pursuant to the requirements of applicable State laws and regulations, the starting salary range for this position is $90-100K USD. Factors which may affect starting pay within this range may include geography/market, skills, education, experience and other qualifications of the successful candidate.
COMPENSATION AND BENEFITS:
Natus offers generous compensation and benefits packages including health benefits, 401k contribution, 7 paid holidays + 2 floating holidays of your choosing, generous paid time off, tuition reimbursement assistance program, eligibility for performance-based bonuses or commissions, where applicable and more.
Be the People part of the Neuro Solution. Apply Today.
EEO STATEMENT:
Natus Medical is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, veteran status, disability, sexual orientation, gender identity, or any other protected status.
INTRODUCTION
FOR MORE THAN 80 YEARS, Natus has been working in collaboration with clinicians to deliver industry-leading neuro solutions that help providers more easily make sense of the body’s signals. Engineered with input from those who have lived the care experience, our technology simplifies complex processes and improves accuracy and efficiency. There is a role for everyone who wants to be part of the innovative solutions at Natus Neuro.
Location: Middleton, WI (Hybrid Role)
ABOUT THE ROLE
We're looking for an experienced Supplier Quality Engineer to help ensure the quality and reliability of the parts, materials, and services that go into our products. In this role, you'll take ownership of supplier quality activities, working directly with suppliers and internal teams to resolve quality issues, improve supplier performance, and maintain compliance with regulatory requirements. You'll be involved in everything from supplier qualification and audits to investigating complex quality issues and supporting new product introductions. This is an opportunity for someone who enjoys problem-solving, working across different teams, and taking responsibility for driving quality improvements.
Manage Supplier Quality & Performance:
- Take ownership of quality activities for an assigned portfolio of suppliers, ensuring compliance with Natus requirements and applicable regulatory standards.
- Qualify and assess suppliers to ensure they meet established quality expectations.
- Monitor supplier performance, identify trends, and work with suppliers to drive improvements.
- Review and assess supplier change notifications to evaluate potential quality impacts.
Investigate Issues & Drive Solutions:
- Lead investigations into supplier-related nonconformances and manage Supplier Corrective Action Requests (SCARs) through resolution.
- Work closely with suppliers to identify root causes, implement corrective actions, and address recurring quality issues.
- Collaborate with Manufacturing, Engineering, Sourcing, Regulatory Affairs, and other teams to resolve supplier challenges and support business needs.
Lead Supplier Audits & Maintain Compliance:
- Plan, schedule, and conduct supplier quality audits to assess compliance with applicable quality and regulatory requirements.
- Prepare audit reports, communicate findings, and work with suppliers to ensure timely closure of identified issues.
- Support regulatory inspections, including FDA and BSI inspections.
Support Projects & Continuous Improvement:
- Support supplier quality activities related to new product introductions, product transfers, and manufacturing changes.
- Identify opportunities to improve supplier quality processes and performance.
- Independently manage assigned activities and projects, delivering against agreed timelines.
- Contribute to a team culture built on accountability, collaboration, continuous improvement, and patient safety.
WHAT WE'RE LOOKING FOR
We're looking for someone with solid supplier quality experience who is comfortable managing their own priorities, working directly with suppliers, and navigating quality challenges in a regulated environment.
REQUIRED EXPERIENCE & QUALIFICATIONS
- Bachelor's degree and a minimum of 5 years of relevant experience in Quality Engineering, Supplier Quality, or Quality Assurance within the medical device industry or another regulated environment.
- Demonstrated experience independently managing supplier qualifications, audits, nonconformance investigations, and corrective actions.
- Strong working knowledge of ISO 13485, FDA quality system requirements, and applicable medical device regulations.
- Qualified ISO 13485 Lead Auditor with experience conducting supplier audits.
- Experience collaborating with Engineering, Manufacturing, Sourcing, and Quality teams.
- Strong communication, organizational, and problem-solving skills.
- Ability to work independently, manage competing priorities, and follow issues through to resolution.
- Willingness and availability to travel to supplier locations within the US.
NICE TO HAVE
- Experience reviewing and approving supplier validation protocols (IQ/OQ/PQ).
- Experience with First Article Inspections (FAI).
INTERESTED IN JOINING NATUS?
If you have experience in supplier quality, enjoy working through complex quality challenges, and want to contribute to maintaining high standards in medical device manufacturing, we'd like to hear from you.
PAY TRANSPARENCY:
Pursuant to the requirements of applicable State laws and regulations, the starting salary range for this position is $90-100K USD. Factors which may affect starting pay within this range may include geography/market, skills, education, experience and other qualifications of the successful candidate.
COMPENSATION AND BENEFITS:
Natus offers generous compensation and benefits packages including health benefits, 401k contribution, 7 paid holidays + 2 floating holidays of your choosing, generous paid time off, tuition reimbursement assistance program, eligibility for performance-based bonuses or commissions, where applicable and more.
Be the People part of the Neuro Solution. Apply Today.
EEO STATEMENT:
Natus Medical is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, veteran status, disability, sexual orientation, gender identity, or any other protected status.
TN Medical Devices Job Roles in Wisconsin
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Search Medical Devices Jobs in WisconsinMedical Devices TN Sponsorship Jobs in Wisconsin: Frequently Asked Questions
Which medical devices companies sponsor TN visas in Wisconsin?
Wisconsin's medical devices employers with TN visa sponsorship activity include Exact Sciences in Madison, Promega Corporation, GE HealthCare's Wisconsin operations, and various contract manufacturers in the Fox Valley and Milwaukee areas. Mid-size device manufacturers focused on diagnostics, surgical instruments, and imaging equipment tend to hire across engineering and regulatory disciplines where TN categories align well with role requirements.
Which cities in Wisconsin have the most medical devices TN sponsorship jobs?
Madison leads due to its concentration of diagnostics and biotech-adjacent device companies, anchored by Exact Sciences and the University of Wisconsin's research commercialization ecosystem. Milwaukee and its suburbs host manufacturing-heavy device employers spanning orthopedics and imaging. The Fox Valley region around Appleton and Oshkosh also has established medical equipment manufacturers that regularly hire engineers and quality professionals.
What types of medical devices roles typically qualify for TN sponsorship?
TN sponsorship in medical devices most commonly applies to roles requiring a specific bachelor's degree or higher in a qualifying field. Engineers (mechanical, electrical, biomedical, manufacturing) and quality assurance or regulatory affairs professionals with science or engineering degrees are frequently eligible. Scientific roles in R&D and product development also align well with TN categories when the degree-to-job-duty connection is clearly documented.
How do I find medical devices TN sponsorship jobs in Wisconsin?
Migrate Mate is built specifically for TN visa holders and lists medical devices roles in Wisconsin where employers have indicated sponsorship willingness. Rather than filtering through general job boards where TN eligibility is rarely disclosed, Migrate Mate surfaces positions relevant to Canadian and Mexican professionals in Wisconsin's device sector, covering engineering, regulatory, and quality roles across Madison, Milwaukee, and surrounding manufacturing corridors.
Are there any Wisconsin-specific considerations for TN sponsorship in medical devices?
Wisconsin's medical devices industry leans heavily on manufacturing and quality operations, so many open roles involve production environments where demonstrating the connection between a professional degree and the specific job duties is important for TN eligibility. Roles classified as technician-level rather than professional-level may not qualify under TN categories, so verifying that the position requires at least a bachelor's degree in a relevant field is an important step before applying.