Medical Devices STEM OPT Jobs in Michigan
Michigan's medical devices sector spans Kalamazoo, Grand Rapids, and the Detroit metro, anchoring companies like Stryker, Gentex, and Autocam Medical. F-1 STEM OPT sponsorship is active across biomedical engineering, regulatory affairs, and quality systems roles, making Michigan one of the more accessible Midwest states for medical devices graduates extending their OPT authorization.
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Get Access To All JobsWhy join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more: US Stryker employee benefits.
Senior Quality Assurance Engineer
Portage, MI
Join a team where your expertise directly impacts patient safety and product performance. As a Senior Quality Assurance Engineer, you’ll lead Emergency Care critical investigations and drive improvements for the Belfast, Northern Ireland site that shapes the future of medical technology. This is a high-impact role for someone passionate about solving complex problems and ensuring quality excellence across the product lifecycle.
Work Flexibility:
Hybrid: candidates must reside within commuting distance of Portage, MI and be able to work onsite several days per week.
What you will do
- Lead product field action assessments from initiation through review and approval, ensuring complete, accurate, and timely documentation.
- Investigate complex product quality issues using structured problem-solving, root cause analysis, and statistical evaluation methods.
- Perform post-market health risk assessments and health hazard evaluations to assess potential product and patient safety risks.
- Develop containment recommendations and corrective actions based on investigation findings, risk assessments, and quality data.
- Author and manage nonconformance and corrective and preventive action records, including defined deliverables, action owners, timelines, and supporting documentation.
- Coordinate investigation and corrective action reviews with Research & Development, Manufacturing, Regulatory, Quality, Marketing, Service, and supplier teams.
- Represent Quality Assurance processes during internal and external audits and maintain compliance with applicable quality system, risk management, and post-market requirements.
What you will need
Required Qualifications
- Bachelor’s degree in science, engineering, or a related discipline.
- Minimum 2 years of experience in quality assurance or customer quality.
- Experience working in a regulated industry, such as medical devices or aerospace.
- Experience conducting post-market quality assessments.
Preferred Qualifications
- Master’s degree in science, engineering, or related discipline.
- Experience conducting product field actions.
- Experience working with ISO 14971, ISO 13485, 21 CFR Part 820, and European Union Medical Device Regulation requirements.
- Six Sigma Green Belt certification or experience with formal investigative techniques.
Compensation
- Salary Range: $77,700 - $129,500 USD Annual
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.
Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more: US Stryker employee benefits.
Senior Quality Assurance Engineer
Portage, MI
Join a team where your expertise directly impacts patient safety and product performance. As a Senior Quality Assurance Engineer, you’ll lead Emergency Care critical investigations and drive improvements for the Belfast, Northern Ireland site that shapes the future of medical technology. This is a high-impact role for someone passionate about solving complex problems and ensuring quality excellence across the product lifecycle.
Work Flexibility:
Hybrid: candidates must reside within commuting distance of Portage, MI and be able to work onsite several days per week.
What you will do
- Lead product field action assessments from initiation through review and approval, ensuring complete, accurate, and timely documentation.
- Investigate complex product quality issues using structured problem-solving, root cause analysis, and statistical evaluation methods.
- Perform post-market health risk assessments and health hazard evaluations to assess potential product and patient safety risks.
- Develop containment recommendations and corrective actions based on investigation findings, risk assessments, and quality data.
- Author and manage nonconformance and corrective and preventive action records, including defined deliverables, action owners, timelines, and supporting documentation.
- Coordinate investigation and corrective action reviews with Research & Development, Manufacturing, Regulatory, Quality, Marketing, Service, and supplier teams.
- Represent Quality Assurance processes during internal and external audits and maintain compliance with applicable quality system, risk management, and post-market requirements.
What you will need
Required Qualifications
- Bachelor’s degree in science, engineering, or a related discipline.
- Minimum 2 years of experience in quality assurance or customer quality.
- Experience working in a regulated industry, such as medical devices or aerospace.
- Experience conducting post-market quality assessments.
Preferred Qualifications
- Master’s degree in science, engineering, or related discipline.
- Experience conducting product field actions.
- Experience working with ISO 14971, ISO 13485, 21 CFR Part 820, and European Union Medical Device Regulation requirements.
- Six Sigma Green Belt certification or experience with formal investigative techniques.
Compensation
- Salary Range: $77,700 - $129,500 USD Annual
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.
STEM OPT Medical Devices Job Roles in Michigan
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Search Medical Devices Jobs in MichiganMedical Devices STEM OPT Sponsorship Jobs in Michigan: Frequently Asked Questions
Which medical devices companies in Michigan sponsor F-1 STEM OPT visas?
Stryker, headquartered in Kalamazoo, is among the most consistent medical devices employers with F-1 STEM OPT hiring history in Michigan. Other active employers include Autocam Medical in Grand Rapids and various contract manufacturers and OEM suppliers clustered in West Michigan. Filing history through DOL Labor Condition Applications gives the clearest picture of which specific employers have active sponsorship programs.
Which Michigan cities have the most medical devices F-1 STEM OPT sponsorship jobs?
Kalamazoo leads given Stryker's large engineering and operations footprint there. Grand Rapids has a dense cluster of medical device contract manufacturers and suppliers. The Detroit metro area, particularly Auburn Hills and Ann Arbor, draws biomedical and regulatory roles tied to both established device companies and university-adjacent startups. West Michigan overall concentrates the highest volume of STEM OPT-eligible device roles in the state.
What types of medical devices roles typically qualify for F-1 STEM OPT sponsorship in Michigan?
Roles with a clear STEM degree requirement are the most straightforward candidates. In Michigan's medical devices sector, that typically includes biomedical engineering, mechanical engineering, quality systems engineering, regulatory affairs, manufacturing engineering, and R&D positions. Software and data roles within device companies, such as embedded systems or software quality assurance, also commonly qualify when tied to a STEM-classified degree program under the DHS STEM Designated Degree Program List.
How do I find medical devices F-1 STEM OPT sponsorship jobs in Michigan?
Migrate Mate filters medical devices jobs in Michigan specifically for F-1 STEM OPT candidates, surfacing employers with verified DOL Labor Condition Application filing history so you can prioritize companies that have actually sponsored STEM OPT workers before. Search by city, role type, or company size to narrow results. Cross-referencing employer LCA data helps confirm sponsorship activity before investing time in an application.
Are there any Michigan-specific considerations for F-1 STEM OPT sponsorship in medical devices?
Michigan employers in medical devices are often subject to FDA quality system regulations, which means roles in quality assurance and regulatory affairs carry compliance expectations that can make degree-match documentation especially important for STEM OPT purposes. Michigan also has a significant tier of smaller contract manufacturers where formal immigration infrastructure may be less developed than at large OEMs like Stryker, so confirming an employer's prior sponsorship history before applying is a practical step.