Quality Assurance Engineer Visa Sponsorship Jobs in Michigan
Michigan's quality assurance engineer job market is anchored by automotive and manufacturing giants like General Motors, Ford, Stellantis, and their supplier networks across Detroit, Warren, and Auburn Hills. Aerospace and medical device firms add demand in Grand Rapids and Ann Arbor. Many of these employers have established visa sponsorship programs for qualified QA engineers.
Find Quality Assurance Engineer JobsOverview
Showing 5 of 27+ Quality Assurance Engineer Jobs in Michigan with Visa Sponsorship
See all Quality Assurance Engineer Jobs in Michigan with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Quality Assurance Engineer Jobs in Michigan with Visa Sponsorship.
Get Access To All JobsINTRODUCTION
At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.
Join us on our One Perrigo journey as we evolve to win in self-care.
DESCRIPTION OVERVIEW
At Perrigo, we are dedicated to making lives better by delivering high-quality, affordable self-care products that consumers trust worldwide. As the Quality Assurance Manager, you will play a critical leadership role in ensuring the safety, quality, and compliance of our products throughout manufacturing, packaging, and product release operations.
This position provides quality oversight for site operations, driving a culture of quality, regulatory compliance, continuous improvement, and operational excellence. The Quality Assurance Manager partners cross-functionally with Operations, Engineering, Maintenance, Laboratory, and Quality teams to identify risks, resolve quality issues, and implement sustainable improvements that enhance product and process performance.
The successful candidate will lead and develop quality professionals, support regulatory and customer audits, provide risk-based decision making, and ensure compliance with cGMP requirements, FDA regulations, and company standards. This role is ideal for a collaborative leader who is passionate about building high-performing teams while advancing quality systems that protect consumers and support business success.
SCOPE OF THE ROLE
- Strong problem-solving skills, and logical approach based on sound judgment and research
- Sound understanding of cGMP/FDA regulations: CFR and FDA guidance documents related to drug manufacturing (21 CFR 210/211).
- Subject matter expertise that extends beyond the area of responsibility
- Manages support for contract or retail customer technical questions, and/or to provide technical impact or risk assessment
- Promotes development and succession planning for direct and indirect reports within area of responsibility
- Manages and leads cross functional continuous improvement opportunities and projects
- Develops and maintains auditing and release procedures which ensure products released for shipment meet company, customer and FDA standards
- Provides risk assessment over significant Quality events
- Works with operations, laboratory, engineering, and maintenance managers and staff to develop, evaluate and implement action plans which maintain or improve product and process quality
- Partners with Site Quality Leadership to align processes with PMI and OTC objectives
- Reviews and approves Standard Operating Procedure updates, change control, and validation reports.
- Leads and guides others in quality driven initiatives in the continuous support of Quality Improvement
- Final quality approver for standard work instruction (SWI) and standard operating procedures (SOP)
- Supports FDA, customer, internal, and other regulatory audits and responses
EXPERIENCE REQUIRED
- Typically, a minimum of 8 years in the field and 4 years supervisory experience. University Degree or equivalent
- Bachelor's degree within related discipline required
- Six or more years’ experience in a regulated industry, pharma preferred
- Demonstrated ability in areas of people leadership and quality leadership
- Excellent written and oral communication skills
BENEFITS
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.
Find out more about Total Rewards at Perrigo.
We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here.
APPLICANTS PLEASE NOTE: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo
INTRODUCTION
At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.
Join us on our One Perrigo journey as we evolve to win in self-care.
DESCRIPTION OVERVIEW
At Perrigo, we are dedicated to making lives better by delivering high-quality, affordable self-care products that consumers trust worldwide. As the Quality Assurance Manager, you will play a critical leadership role in ensuring the safety, quality, and compliance of our products throughout manufacturing, packaging, and product release operations.
This position provides quality oversight for site operations, driving a culture of quality, regulatory compliance, continuous improvement, and operational excellence. The Quality Assurance Manager partners cross-functionally with Operations, Engineering, Maintenance, Laboratory, and Quality teams to identify risks, resolve quality issues, and implement sustainable improvements that enhance product and process performance.
The successful candidate will lead and develop quality professionals, support regulatory and customer audits, provide risk-based decision making, and ensure compliance with cGMP requirements, FDA regulations, and company standards. This role is ideal for a collaborative leader who is passionate about building high-performing teams while advancing quality systems that protect consumers and support business success.
SCOPE OF THE ROLE
- Strong problem-solving skills, and logical approach based on sound judgment and research
- Sound understanding of cGMP/FDA regulations: CFR and FDA guidance documents related to drug manufacturing (21 CFR 210/211).
- Subject matter expertise that extends beyond the area of responsibility
- Manages support for contract or retail customer technical questions, and/or to provide technical impact or risk assessment
- Promotes development and succession planning for direct and indirect reports within area of responsibility
- Manages and leads cross functional continuous improvement opportunities and projects
- Develops and maintains auditing and release procedures which ensure products released for shipment meet company, customer and FDA standards
- Provides risk assessment over significant Quality events
- Works with operations, laboratory, engineering, and maintenance managers and staff to develop, evaluate and implement action plans which maintain or improve product and process quality
- Partners with Site Quality Leadership to align processes with PMI and OTC objectives
- Reviews and approves Standard Operating Procedure updates, change control, and validation reports.
- Leads and guides others in quality driven initiatives in the continuous support of Quality Improvement
- Final quality approver for standard work instruction (SWI) and standard operating procedures (SOP)
- Supports FDA, customer, internal, and other regulatory audits and responses
EXPERIENCE REQUIRED
- Typically, a minimum of 8 years in the field and 4 years supervisory experience. University Degree or equivalent
- Bachelor's degree within related discipline required
- Six or more years’ experience in a regulated industry, pharma preferred
- Demonstrated ability in areas of people leadership and quality leadership
- Excellent written and oral communication skills
BENEFITS
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.
Find out more about Total Rewards at Perrigo.
We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here.
APPLICANTS PLEASE NOTE: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo
Quality Assurance Engineer Job Roles in Michigan
See all Quality Assurance Engineer Jobs in Michigan
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Quality Assurance Engineer Jobs in MichiganQuality Assurance Engineer Jobs in Michigan: Frequently Asked Questions
Which companies sponsor visas for quality assurance engineers in Michigan?
Michigan's largest visa sponsors for quality assurance engineers are concentrated in the automotive sector. General Motors, Ford, Stellantis, Aptiv, BorgWarner, and Magna International have all filed H-1B visa Labor Condition Applications for QA-related roles. Medical device companies like Stryker and Gentex, along with automotive software suppliers in the Ann Arbor and Troy corridors, also sponsor QA engineering positions regularly.
Which visa types are most common for quality assurance engineer roles in Michigan?
The H-1B is the most common visa for quality assurance engineers in Michigan, as QA engineering typically qualifies as a specialty occupation requiring at least a bachelor's degree in engineering, computer science, or a related field. Candidates already holding an L-1B intracompany transfer visa or TN visa status (for Canadian and Mexican nationals) can also fill QA roles without entering the H-1B lottery.
Which cities in Michigan have the most quality assurance engineer sponsorship jobs?
The Detroit metropolitan area, including Warren, Troy, Auburn Hills, and Dearborn, accounts for the majority of QA engineer sponsorship activity in Michigan due to the density of automotive OEMs and Tier 1 suppliers. Grand Rapids has a growing presence driven by medical device and manufacturing firms. Ann Arbor attracts QA roles tied to automotive technology and university-affiliated research and development employers.
How to find quality assurance engineer visa sponsorship jobs in Michigan?
Migrate Mate is built specifically for international candidates seeking visa sponsorship and lets you filter quality assurance engineer roles by state, so you can browse verified Michigan opportunities without sorting through listings from employers who don't sponsor. Given how concentrated Michigan's QA market is around automotive and manufacturing hubs, filtering by city alongside sponsorship status helps narrow results to the most relevant openings.
Are there any Michigan-specific considerations for quality assurance engineer visa sponsorship candidates?
Michigan's QA engineering market is heavily tied to automotive production cycles, so hiring often accelerates ahead of new model launches and program kickoffs. The University of Michigan and Michigan State University feed significant engineering talent pipelines, which means OPT and STEM OPT candidates are common in the applicant pool. Employers in regulated industries like automotive safety systems and medical devices may require additional background checks or export control clearance that can affect sponsorship timelines.
What is the prevailing wage for sponsored quality assurance engineer jobs in Michigan?
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.