Quality Supervisor Visa Sponsorship Jobs in Wisconsin
Wisconsin's quality supervisor roles span food manufacturing, medical devices, and industrial equipment, with employers like Oshkosh Corporation, Bemis Manufacturing, and Quaker Chemical operating across Green Bay, Milwaukee, and the Fox Valley corridor. International candidates with quality management credentials and relevant manufacturing experience are consistently sought by Wisconsin employers willing to support visa sponsorship.
Find Quality Supervisor JobsOverview
Showing 5 of 44+ Quality Supervisor Jobs in Wisconsin with Visa Sponsorship
See all 44+ Quality Supervisor Jobs in Wisconsin with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Quality Supervisor Jobs in Wisconsin with Visa Sponsorship.
Get Access To All JobsSupervisor - Quality Assurance
Position Summary:
- Shift: M-F 8am-5pm
- Location: Madison, WI
- 100% Onsite
Catalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting customers from research through early‑ and mid‑stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700‑square‑foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single‑use systems to enable rapid scale‑up and customization. The site is home to Catalent’s proprietary GPEx® and GPEx® Lightning technologies, which are used to generate high‑yielding mammalian cell lines for biologic therapies, and supports production scales ranging from 50 to 4,000 liters for clinical manufacturing. Following a $45 million expansion announced in 2025, the Madison site has significantly increased capacity, added new equipment, and created approximately 200 highly skilled biohealth jobs, further strengthening its role within Catalent’s global biologics network and Wisconsin’s growing life sciences ecosystem.
We have an opportunity for a Supervisor - Quality Assurance to join our team. In this role, you will provide oversight to ensure the site Deviation, Corrective and Preventive Action (CAPA), and Change Control programs meet regulatory requirements, customer expectations, and internal quality standards. You will manage day-to-day activities, prioritize tasks, and ensure timely completion of investigations and actions. This position plays a key role in maintaining and improving quality systems, supporting audits, and fostering a culture of compliance and continuous improvement.
The Role
- Lead and oversee Deviation, CAPA, and Change Control programs to ensure compliance with regulatory requirements, quality standards, and customer expectations.
- Manage the full lifecycle of investigations, CAPAs, and change controls, including risk assessments, root cause analysis, impact evaluations, and effectiveness checks.
- Serve as the site Subject Matter Expert for Quality Systems, providing guidance, training, and support on compliance, investigations, and continuous improvement initiatives.
- Monitor quality metrics and trends, drive process improvements, and lead cross-functional governance forums to ensure accountability and timely resolution of issues.
- Support regulatory inspections, customer audits, and internal audits while fostering a culture of quality, compliance, and operational excellence.
Minimum Requirements
- Doctorate Degree in a STEM discipline with a minimum of 2 years of related experience, OR
- Master's, Bachelor’s, or Associate’s Degree in a STEM discipline with a minimum of 4 years of related experience, AND
- Leadership experience of 0-2 years.
- Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.
Preferred Skills & Background
- Knowledge in Trackwise.
- Ability to manage and support a team of three direct reports.
Why You Should Join Catalent
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition Reimbursement.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
Supervisor - Quality Assurance
Position Summary:
- Shift: M-F 8am-5pm
- Location: Madison, WI
- 100% Onsite
Catalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting customers from research through early‑ and mid‑stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700‑square‑foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single‑use systems to enable rapid scale‑up and customization. The site is home to Catalent’s proprietary GPEx® and GPEx® Lightning technologies, which are used to generate high‑yielding mammalian cell lines for biologic therapies, and supports production scales ranging from 50 to 4,000 liters for clinical manufacturing. Following a $45 million expansion announced in 2025, the Madison site has significantly increased capacity, added new equipment, and created approximately 200 highly skilled biohealth jobs, further strengthening its role within Catalent’s global biologics network and Wisconsin’s growing life sciences ecosystem.
We have an opportunity for a Supervisor - Quality Assurance to join our team. In this role, you will provide oversight to ensure the site Deviation, Corrective and Preventive Action (CAPA), and Change Control programs meet regulatory requirements, customer expectations, and internal quality standards. You will manage day-to-day activities, prioritize tasks, and ensure timely completion of investigations and actions. This position plays a key role in maintaining and improving quality systems, supporting audits, and fostering a culture of compliance and continuous improvement.
The Role
- Lead and oversee Deviation, CAPA, and Change Control programs to ensure compliance with regulatory requirements, quality standards, and customer expectations.
- Manage the full lifecycle of investigations, CAPAs, and change controls, including risk assessments, root cause analysis, impact evaluations, and effectiveness checks.
- Serve as the site Subject Matter Expert for Quality Systems, providing guidance, training, and support on compliance, investigations, and continuous improvement initiatives.
- Monitor quality metrics and trends, drive process improvements, and lead cross-functional governance forums to ensure accountability and timely resolution of issues.
- Support regulatory inspections, customer audits, and internal audits while fostering a culture of quality, compliance, and operational excellence.
Minimum Requirements
- Doctorate Degree in a STEM discipline with a minimum of 2 years of related experience, OR
- Master's, Bachelor’s, or Associate’s Degree in a STEM discipline with a minimum of 4 years of related experience, AND
- Leadership experience of 0-2 years.
- Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.
Preferred Skills & Background
- Knowledge in Trackwise.
- Ability to manage and support a team of three direct reports.
Why You Should Join Catalent
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition Reimbursement.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
Quality Supervisor Job Roles in Wisconsin
See all 44+ Quality Supervisor Jobs in Wisconsin
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Quality Supervisor Jobs in WisconsinQuality Supervisor Jobs in Wisconsin: Frequently Asked Questions
Which companies sponsor visas for quality supervisors in Wisconsin?
Wisconsin manufacturers with documented H-1B visa sponsorship histories include Oshkosh Corporation, Rockwell Automation, Bemis Manufacturing, and Johnson Controls. Medical device firms operating in the Milwaukee area, such as Baxter and GE Healthcare affiliates, also sponsor quality-focused roles. Food processing companies concentrated in the Green Bay and Fox Valley regions represent another consistent source of quality supervisor sponsorship, particularly for candidates with food safety certifications like HACCP or SQF.
Which visa types are most common for quality supervisor roles in Wisconsin?
The H-1B is the most common visa for quality supervisors in Wisconsin, provided the role requires a specific bachelor's degree in engineering, manufacturing science, or a closely related field. Candidates with advanced degrees may pursue an EB-2 immigrant visa through PERM labor certification. Some multinational manufacturers with Wisconsin operations also transfer quality personnel through L-1B intracompany transferee visas when the candidate holds specialized proprietary knowledge.
Which cities in Wisconsin have the most quality supervisor sponsorship jobs?
Milwaukee is the largest concentration point, anchored by its industrial manufacturing and life sciences base. The Fox Valley corridor, spanning Appleton, Oshkosh, and Neenah, hosts dense paper, packaging, and precision manufacturing operations that regularly hire quality supervisors. Green Bay's food processing and packaging sector adds meaningful volume. Madison sees demand from medical device and research-adjacent manufacturing firms tied to the University of Wisconsin ecosystem.
How to find quality supervisor visa sponsorship jobs in Wisconsin?
Migrate Mate aggregates quality supervisor visa sponsorship jobs filtered specifically to Wisconsin, allowing you to search by city, employer, and visa type without sifting through listings that don't offer sponsorship. Given Wisconsin's spread across manufacturing corridors in Milwaukee, the Fox Valley, and Green Bay, filtering by location on Migrate Mate helps match your specialization, whether food safety, medical devices, or industrial equipment, to employers actively sponsoring in your target area.
Are there state-specific factors that affect quality supervisor sponsorship in Wisconsin?
Wisconsin's prevailing wage requirements under the H-1B program are benchmarked to Department of Labor wage surveys for specific counties, so compensation for quality supervisor roles varies noticeably between the Milwaukee metro and rural manufacturing towns. The state's strong technical college system, including FVTC and WCTC, creates a competitive local talent pool, meaning employers sponsoring international candidates generally prioritize applicants with specialized certifications, such as ASQ credentials or ISO auditing experience, that are harder to source domestically.
What is the prevailing wage for sponsored quality supervisor 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.