Biotech & Pharma Green Card Sponsorship Jobs in Michigan
Michigan's biotech and pharma sector spans Ann Arbor's research corridor, Kalamazoo's established pharma base anchored by Pfizer and Stryker's broader medtech ecosystem, and Grand Rapids' growing life sciences cluster. Employers across the state sponsor Green Card visas for research scientists, regulatory specialists, and manufacturing professionals, making Michigan a serious destination for international talent in the industry.
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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
Green Card Biotech & Pharma Job Roles in Michigan
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Search Biotech & Pharma Jobs in MichiganBiotech & Pharma Green Card Sponsorship Jobs in Michigan: Frequently Asked Questions
Which biotech & pharma companies sponsor Green Card visas in Michigan?
Michigan has a concentration of life sciences employers with documented Green Card sponsorship histories. Pfizer's Kalamazoo operations, Perrigo, Kalsec, and several contract research organizations based in the Ann Arbor area have filed Green Card petitions through PERM labor certification. University-affiliated research institutes and hospital systems like University of Michigan Health also sponsor researchers and clinical specialists for permanent residence.
Which cities in Michigan have the most biotech & pharma Green Card sponsorship jobs?
Ann Arbor leads Michigan for biotech and pharma Green Card opportunities, driven by the University of Michigan's research infrastructure and a dense cluster of life sciences startups and CROs. Kalamazoo is the second-strongest market, historically anchored by large pharma manufacturing. Grand Rapids has grown steadily, supported by Spectrum Health's research operations and medical device companies with permanent residency sponsorship programs.
What types of biotech & pharma roles typically qualify for Green Card sponsorship in Michigan?
Roles requiring specialized education, typically a master's or doctoral degree, are most commonly sponsored. These include research scientists in oncology, immunology, and drug discovery, regulatory affairs specialists, bioprocess engineers, clinical data managers, and quality assurance professionals. Positions tied to proprietary research pipelines or manufacturing processes are particularly likely to attract EB-2 or EB-3 sponsorship because the specialized knowledge is difficult to replace with a domestic hire.
How do I find biotech & pharma Green Card sponsorship jobs in Michigan?
Migrate Mate lets you filter specifically for biotech and pharma roles in Michigan where employers are actively offering Green Card sponsorship, which removes the guesswork of cold-applying to companies that don't sponsor. Because sponsorship willingness is built into the search filters, you can focus your applications on Michigan employers, from Ann Arbor CROs to Kalamazoo pharma manufacturers, that have a genuine track record of supporting permanent residency.
Are there any Michigan-specific considerations for Green Card sponsorship in biotech & pharma?
Michigan's biotech sector includes a notable proportion of academic medical centers and university spin-outs, particularly around Ann Arbor, which often use EB-1A or EB-2 NIW pathways for senior researchers rather than the employer-sponsored PERM route. For industry roles, Michigan's relatively lower cost base compared to coastal biotech hubs can influence whether smaller employers find the PERM process financially practical. Processing timelines through the Department of Labor are national, not state-specific.
What is the prevailing wage for Green Card biotech & pharma 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.