Regulatory Affairs Analyst Jobs in Wisconsin
Regulatory affairs analyst jobs in Wisconsin are concentrated in Madison and Milwaukee, where life sciences anchors like Abbott, Exact Sciences, and GE HealthCare maintain significant operations, and demand runs from entry-level specialists through senior compliance leads. The most active specialties are FDA regulatory submissions, quality management systems, and medical device compliance, reflecting Wisconsin's deep roots in diagnostics, medical technology, and pharmaceutical manufacturing. Wisconsin is among the more active Midwest markets for this role, with consistent openings across both established corporations and growing biotech firms. Scan the live roles below and apply to whichever ones fit.
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The Role and Your Impact:
Welcome to the role of North America Regulatory Affairs Senior Manager, Food and Beverage where you will lead a team in a people manager role, leading and developing regulatory professionals who help turn science and regulation into real-world impact. The team enables safe, compliant growth and innovation by translating evolving food regulations into clear, actionable guidance for commercial, technical, and operational teams across the US and Canada.
As the manager, you will provide direction, prioritization, coaching, and stakeholder alignment while ensuring strong execution on dossiers, customer questions, product launches, digitalization, change management, regulatory intelligence, and process improvement. The team works closely with other areas of the business.
We are strengthening regulatory intelligence capabilities, digitalizing and harmonizing ways of working, and building expertise in emerging ingredients, labeling/claims developments, and new regulatory pathways across North America.
Key Responsibilities in this role:
- This position works with a high level of autonomy and is responsible for leading North America Regulatory Affairs activities and people priorities that enable compliant business growth, customer support, innovation, and operational excellence across the US and Canada.
- Lead, coach, and develop direct reports, including setting priorities, clarifying expectations, supporting performance and development conversations, and building capabilities across US and Canada regulatory topics.
- Provide strategic and operational regulatory leadership for relevant food ingredient and food segments in the US and Canada; monitor, interpret, and communicate regulatory changes and potential business impact to internal stakeholders.
- Ensure timely , accurate regulatory guidance to internal stakeholders and customers regarding product and ingredient regulatory status, specifications, labeling/claims as applicable, and manufacturing/process considerations; support team escalation and decision-making on complex topics.
- Oversee and support preparation of regulatory dossiers, notifications, submissions, and compliance documentation for the US and Canada in collaboration with Global Regulatory Affairs and local resources.
What You’ll Need to be Successful:
Required Qualifications:
- BS degree; or Master’s degree preferred in Engineering , Food Science, Pharmacy, Nutrition, Chemistry, Biology, or related Natural Sciences.
- 15+ years in Regulatory Affairs within the food industry or a related regulated industry
- Experience supporting US and/or Canada regulatory deliverables such as enzymes, cultures, probiotics, ingredients, labeling/claims support, dossiers, notifications, and customer/regulatory documentation. Leadership experience is required , including coaching, prioritization, performance management, and development of regulatory professionals.
Core Competencies:
- Strong regulatory judgment, stakeholder management, people leadership, project prioritization, and communication skills. Strong computer/IT skills, including working knowledge of Microsoft Office programs; experience with digital tools, reporting, dashboards, or workflow optimization is a plus.
- English (read/write/speak). Spanish is a plus.
- Cross cultural awareness and experience working in a global environment.
What We Offer
At Novonesis, you will join a purpose-driven organization where innovation and collaboration are at the heart of what we do. We offer opportunities to work on impactful projects, develop your expertise, and grow your career in a supportive team environment.
You will have the opportunity to:
- Partner with business, technical, and innovation teams to define compliant regulatory pathways for new products, line extensions, and process changes, while ensuring regulatory deliverables are prioritized, resourced, tracked, and communicated.
- Represent North America Regulatory Affairs in relevant industry or trade association activities, as needed, and build external regulatory insight to support business continuity and advocacy priorities.
- Drive continuous improvement, digital transformation, harmonized ways of working, reporting, and internal training to improve transparency, efficiency, and quality of regulatory support.
- Support procurement-related regulatory processes and supplier/customer documentation needs where regulatory input is required .
Ways of Working:
Hybrid : This role is primarily office-based in West Allis, Wisconsin , with
flexibility to work from home when needed.
Travel : Approximately 30%, including team engagement, stakeholder meetings, customer or industry interactions, and site/business needs.
Compensation & Benefits:
- Expected base salary range: $145,000 – $165,000 based on experience
- 401(k) with up to a 9% company contribution
- Minimum of 3 weeks of vacation plus 12 holidays and 2 weeks of Wellness Time
- Health, Dental, Vision & Life insurance
- Healthcare savings account option
- Employee assistance program
- Parental leave
- Tuition reimbursement
- All benefits begin on your first day
Relevant Information: Application deadline: 7/30/26
Our purpose guides the way
In Novonesis, we know that solutions rooted in biology can help solve humanity’s biggest challenges. Since we began more than a century ago, this has been our guide. It’s how we've gotten so far. And it’s how we'll impact the future. Now, more than ever, the world needs change. And with biosolutions, the possibilities for transformation are endless. If our purpose resonates with you, we encourage you to apply.
Opportunities for everyone
We are committed to an inclusive recruitment process and equal opportunity for all applicants. Therefore we ask you to apply without a cover letter or photo and instead include a few sentences in your CV explaining your motivation for applying.
We make all employment decisions based on business needs and welcome candidates with a wide range of backgrounds, including ethnicity, religion, gender, sexual orientation, age, disability, or veteran status.
Explore other openings
If this position isn’t the right fit, you may still find other opportunities with us. You’re welcome to explore open roles or create a job agent to stay connected with future opportunities at novonesis.com/Career
Interested in a career that matters?

The Role and Your Impact:
Welcome to the role of North America Regulatory Affairs Senior Manager, Food and Beverage where you will lead a team in a people manager role, leading and developing regulatory professionals who help turn science and regulation into real-world impact. The team enables safe, compliant growth and innovation by translating evolving food regulations into clear, actionable guidance for commercial, technical, and operational teams across the US and Canada.
As the manager, you will provide direction, prioritization, coaching, and stakeholder alignment while ensuring strong execution on dossiers, customer questions, product launches, digitalization, change management, regulatory intelligence, and process improvement. The team works closely with other areas of the business.
We are strengthening regulatory intelligence capabilities, digitalizing and harmonizing ways of working, and building expertise in emerging ingredients, labeling/claims developments, and new regulatory pathways across North America.
Key Responsibilities in this role:
- This position works with a high level of autonomy and is responsible for leading North America Regulatory Affairs activities and people priorities that enable compliant business growth, customer support, innovation, and operational excellence across the US and Canada.
- Lead, coach, and develop direct reports, including setting priorities, clarifying expectations, supporting performance and development conversations, and building capabilities across US and Canada regulatory topics.
- Provide strategic and operational regulatory leadership for relevant food ingredient and food segments in the US and Canada; monitor, interpret, and communicate regulatory changes and potential business impact to internal stakeholders.
- Ensure timely , accurate regulatory guidance to internal stakeholders and customers regarding product and ingredient regulatory status, specifications, labeling/claims as applicable, and manufacturing/process considerations; support team escalation and decision-making on complex topics.
- Oversee and support preparation of regulatory dossiers, notifications, submissions, and compliance documentation for the US and Canada in collaboration with Global Regulatory Affairs and local resources.
What You’ll Need to be Successful:
Required Qualifications:
- BS degree; or Master’s degree preferred in Engineering , Food Science, Pharmacy, Nutrition, Chemistry, Biology, or related Natural Sciences.
- 15+ years in Regulatory Affairs within the food industry or a related regulated industry
- Experience supporting US and/or Canada regulatory deliverables such as enzymes, cultures, probiotics, ingredients, labeling/claims support, dossiers, notifications, and customer/regulatory documentation. Leadership experience is required , including coaching, prioritization, performance management, and development of regulatory professionals.
Core Competencies:
- Strong regulatory judgment, stakeholder management, people leadership, project prioritization, and communication skills. Strong computer/IT skills, including working knowledge of Microsoft Office programs; experience with digital tools, reporting, dashboards, or workflow optimization is a plus.
- English (read/write/speak). Spanish is a plus.
- Cross cultural awareness and experience working in a global environment.
What We Offer
At Novonesis, you will join a purpose-driven organization where innovation and collaboration are at the heart of what we do. We offer opportunities to work on impactful projects, develop your expertise, and grow your career in a supportive team environment.
You will have the opportunity to:
- Partner with business, technical, and innovation teams to define compliant regulatory pathways for new products, line extensions, and process changes, while ensuring regulatory deliverables are prioritized, resourced, tracked, and communicated.
- Represent North America Regulatory Affairs in relevant industry or trade association activities, as needed, and build external regulatory insight to support business continuity and advocacy priorities.
- Drive continuous improvement, digital transformation, harmonized ways of working, reporting, and internal training to improve transparency, efficiency, and quality of regulatory support.
- Support procurement-related regulatory processes and supplier/customer documentation needs where regulatory input is required .
Ways of Working:
Hybrid : This role is primarily office-based in West Allis, Wisconsin , with
flexibility to work from home when needed.
Travel : Approximately 30%, including team engagement, stakeholder meetings, customer or industry interactions, and site/business needs.
Compensation & Benefits:
- Expected base salary range: $145,000 – $165,000 based on experience
- 401(k) with up to a 9% company contribution
- Minimum of 3 weeks of vacation plus 12 holidays and 2 weeks of Wellness Time
- Health, Dental, Vision & Life insurance
- Healthcare savings account option
- Employee assistance program
- Parental leave
- Tuition reimbursement
- All benefits begin on your first day
Relevant Information: Application deadline: 7/30/26
Our purpose guides the way
In Novonesis, we know that solutions rooted in biology can help solve humanity’s biggest challenges. Since we began more than a century ago, this has been our guide. It’s how we've gotten so far. And it’s how we'll impact the future. Now, more than ever, the world needs change. And with biosolutions, the possibilities for transformation are endless. If our purpose resonates with you, we encourage you to apply.
Opportunities for everyone
We are committed to an inclusive recruitment process and equal opportunity for all applicants. Therefore we ask you to apply without a cover letter or photo and instead include a few sentences in your CV explaining your motivation for applying.
We make all employment decisions based on business needs and welcome candidates with a wide range of backgrounds, including ethnicity, religion, gender, sexual orientation, age, disability, or veteran status.
Explore other openings
If this position isn’t the right fit, you may still find other opportunities with us. You’re welcome to explore open roles or create a job agent to stay connected with future opportunities at novonesis.com/Career
See All 11 Regulatory Affairs Analyst Jobs in Wisconsin
Find roles in Wisconsin that match your experience and apply in just a few clicks.
Find JobsRegulatory Affairs Analyst Jobs by City in Wisconsin
Where Wisconsin roles are concentrated, by current openings.
Regulatory Affairs Analyst Job Market in Wisconsin
A snapshot from current Wisconsin openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Manufacturing
- Biotechnology & Pharmaceuticals
What Wisconsin Employers Look For
The qualifications that appear most often in regulatory affairs analyst jobs across Wisconsin.
- Bachelor's degree in life sciences, engineering, chemistry, or a closely related field
- Experience preparing FDA submissions including 510(k), PMA, or IND applications
- Working knowledge of FDA regulations, ISO 13485, and quality management systems
- Familiarity with medical device or pharmaceutical manufacturing environments in regulated industries
- Strong technical writing skills for regulatory documents, SOPs, and compliance reports
- Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professionals Society preferred
Regulatory Affairs Analyst Jobs in Wisconsin: Frequently Asked Questions
How do you become a regulatory affairs analyst in Wisconsin?
Most Wisconsin employers require a bachelor's degree in a life science, engineering, or chemistry discipline as the foundation for entry into regulatory affairs. Wisconsin does not issue a state-specific license for regulatory affairs analysts, so hiring decisions center on education, relevant industry experience, and professional credentials. Earning a Regulatory Affairs Certification from the Regulatory Affairs Professionals Society strengthens competitiveness considerably, particularly for roles in medical device and pharmaceutical companies concentrated in the Madison and Milwaukee corridors.
Which companies hire regulatory affairs analysts in Wisconsin?
Employers hiring regulatory affairs analysts in Wisconsin right now include Werfen, Novonesis, and Merck KGaA, based on current listings on Migrate Mate as of July 2026. Wisconsin's strong medical device and diagnostics manufacturing base, particularly around Madison, keeps demand for regulatory talent fairly consistent throughout the year.
Which Wisconsin cities have the most regulatory affairs analyst jobs?
The cities with the most regulatory affairs analyst openings in Wisconsin are Waukesha, Marinette, and Milwaukee. This distribution reflects Madison's dense concentration of life sciences and medical technology companies, Milwaukee's established manufacturing and healthcare sectors, and the surrounding suburbs where major device and pharmaceutical employers have sited their compliance and regulatory teams.
Are there remote regulatory affairs analyst jobs in Wisconsin?
Yes, and more than most fields. Regulatory affairs work is largely document-driven and desk-based, making it well suited to remote and hybrid arrangements. About 50% of regulatory affairs analyst openings tied to Wisconsin are remote or hybrid as of July 2026, reflecting the analytical and writing-heavy nature of the role. Submission coordination, labeling review, and regulatory strategy work are the functions most commonly offered on a fully remote basis.
How can I get hired as a regulatory affairs analyst in Wisconsin with little or no experience?
The most realistic entry path is a quality assurance or regulatory affairs coordinator role at a Wisconsin medical device or diagnostic company, where document control and SOP management build foundational skills. Companies like Abbott and GE HealthCare periodically hire new graduates into quality operations rotations that ladder into regulatory work. A science degree combined with an internship in a regulated manufacturing environment, or a lateral move from a quality technician or clinical research coordinator role, gives candidates a concrete edge when applying for junior analyst positions.
Where can I find and apply to regulatory affairs analyst jobs in Wisconsin?
You can find and apply to regulatory affairs analyst jobs in Wisconsin on Migrate Mate, which lists current Wisconsin openings updated regularly. Search the available roles, find the ones that match your background and the industries you want to work in, and apply directly to the listings that fit.
See All 11 Regulatory Affairs Analyst Jobs in Wisconsin
Find roles in Wisconsin that match your experience and apply in just a few clicks.
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