Medical Devices Green Card Sponsorship Jobs in Wisconsin
Wisconsin's medical devices sector, anchored by companies like Exact Sciences, Promega, and Spacelabs Medical, offers real pathways to Green Card sponsorship for qualified international professionals. Major hiring activity concentrates in Madison, Milwaukee, and the Fox Valley corridor. Roles in engineering, regulatory affairs, and quality systems are among the most active for employer-sponsored permanent residency.
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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.
Green Card Medical Devices Job Roles in Wisconsin
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Search Medical Devices Jobs in WisconsinMedical Devices Green Card Sponsorship Jobs in Wisconsin: Frequently Asked Questions
Which medical devices companies sponsor Green Card visas in Wisconsin?
Several established medical devices employers in Wisconsin have documented histories of Green Card sponsorship through PERM labor certification. Exact Sciences in Madison, Promega Corporation, Spacelabs Medical, and Plexus Corp in Neenah are among the larger employers with international workforces. Sponsorship decisions are made case by case based on role, department needs, and individual qualifications, so no outcome is guaranteed.
Which cities in Wisconsin have the most medical devices Green Card sponsorship jobs?
Madison leads Wisconsin for medical devices sponsorship activity, driven by its concentration of life sciences and diagnostics companies alongside the University of Wisconsin research ecosystem. Milwaukee is the second major hub, with manufacturing-oriented medical devices employers. The Fox Valley region, particularly Neenah and Appleton, hosts contract manufacturing and electronics-focused medical devices firms that regularly hire internationally.
What types of medical devices roles typically qualify for Green Card sponsorship?
Roles requiring specialized education and technical expertise are the most commonly sponsored. These include quality engineers, regulatory affairs specialists, R&D engineers, software engineers working on device software, manufacturing process engineers, and clinical specialists with advanced degrees. Positions tied to FDA compliance, product development, and design verification tend to attract sponsorship because the required skill sets are specific and in demand.
How do I find medical devices Green Card sponsorship jobs in Wisconsin?
Migrate Mate is built specifically for international professionals seeking Green Card sponsorship roles and filters jobs by visa type, industry, and state. Searching for medical devices positions in Wisconsin on Migrate Mate surfaces employers who have sponsored Green Cards in this sector, saving significant time compared to manually researching individual companies. Combining that with targeted outreach to Wisconsin-based medical devices employers strengthens your search.
Are there any Wisconsin-specific considerations for Green Card sponsorship in medical devices?
Wisconsin's medical devices industry has a strong manufacturing and quality focus, which means many sponsored roles fall under EB-2 or EB-3 categories depending on degree requirements and position level. Because the state's labor market is smaller than coastal hubs, employers sometimes face a more straightforward PERM recruitment process, though timelines still depend on prevailing wage determinations and USCIS processing backlogs. Working with an immigration attorney familiar with Wisconsin employers is advisable.
What is the prevailing wage for Green Card medical devices jobs in Wisconsin?
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.