Biotech & Pharma Visa Sponsorship Jobs in Michigan
Michigan's biotech and pharmaceutical industry centers around Ann Arbor and Grand Rapids, with major employers like Pfizer, Stryker, and Perrigo offering visa sponsorship opportunities. The state's research universities, including University of Michigan, create a strong pipeline for international talent in drug development, medical devices, and clinical research roles.
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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
Biotech & Pharma Job Roles in Michigan
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Search Biotech & Pharma Jobs in MichiganBiotech & Pharma Jobs in Michigan: Frequently Asked Questions
Which biotech & pharma companies in Michigan sponsor work visas?
Major visa sponsors include Pfizer (Kalamazoo), Stryker (Kalamazoo), Perrigo (Grand Rapids), and Merck (West Point). University of Michigan's research programs and smaller biotech firms in Ann Arbor also frequently sponsor H-1B visa and other work visas for scientists, researchers, and clinical professionals.
How to find biotech & pharma visa sponsorship jobs in Michigan?
Use Migrate Mate to filter biotech and pharmaceutical positions specifically in Michigan that offer visa sponsorship. Focus on Ann Arbor and Grand Rapids metro areas where most opportunities are concentrated. Target research institutions, medical device companies, and pharmaceutical manufacturers with established sponsorship histories.
What visa types are most common for biotech & pharma roles in Michigan?
H-1B visas dominate for scientists, research associates, and regulatory affairs specialists. O-1 visas are used for distinguished researchers and PhD-level positions at University of Michigan. TN visas work well for Canadian and Mexican professionals in qualifying scientific roles, while L-1 visas serve international pharmaceutical companies with Michigan operations.
Which Michigan cities have the most biotech & pharma visa sponsorship opportunities?
Ann Arbor leads with University of Michigan research programs and numerous biotech startups. Kalamazoo follows with Pfizer and Stryker headquarters. Grand Rapids offers opportunities with Perrigo and medical device manufacturers. Detroit metro area has emerging life sciences companies, while Portage hosts several pharmaceutical operations.
Are there special considerations for biotech professionals seeking visa sponsorship in Michigan?
Michigan's proximity to University of Michigan creates strong academic-industry partnerships, making PhD credentials particularly valuable. The state's focus on medical devices and generic pharmaceuticals means regulatory affairs and manufacturing experience are in high demand. Winter climate considerations may affect international candidates from warmer regions.
What is the prevailing wage for sponsored 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.