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.
Find JobsOverview
Showing 5 of 8+ Regulatory Affairs Analyst jobs









Location: Sheboygan, WI
Work Arrangement: Hybrid or Onsite. In office at least 3 times per week.
Reports To: VP, Global Quality Assurance
Travel: Up to 25%
Leadership Role: Yes
Relocation Assistance: Available for candidates relocating within commuting distance
Sponsorship: Current or future sponsorship is not available for this position. Candidates must be legally authorized to work in the United States without sponsorship.
Quick Review:
To be successful in this role, you will generally have:
- Bachelor's degree in a scientific discipline
- 15+ years of Regulatory Affairs experience
- 10+ years leading Regulatory teams
- Experience within consumer products, personal care, home care, chemicals, OTC, packaging, or related regulated industries
- Experience with global regulatory requirements and regulatory agencies
Rockline Industries is a privately held manufacturer and distributor of consumer packaged goods serving customers around the world. We combine the stability of an established global organization with the agility, accessibility, and collaborative culture of a privately owned company.
In this role, you will have the opportunity to:
- Influence regulatory strategy across multiple global markets
- Support innovation, product development, and commercialization efforts
- Partner directly with executive leadership on strategic business initiatives
- Lead a global regulatory affairs function with broad organizational impact
- Shape compliance, sustainability, and product stewardship strategies that support future growth
Essential Accountabilities:
As Director, Global Regulatory Affairs, you will develop and execute Rockline's global regulatory strategy to support product compliance, innovation, business continuity, and growth across international markets.
Regulatory Strategy & Business Leadership
- Develop and implement Rockline's global regulatory strategy aligned with business growth objectives
- Assess emerging regulatory trends and evaluate potential business impacts across global markets
- Establish regulatory roadmaps that support growth while minimizing compliance and business risks
- Support innovation, acquisitions, commercialization efforts, and market expansion initiatives
- Provide executive leadership with timely assessments of regulatory opportunities, changes, and risks
Global Compliance & Product Stewardship
- Ensure compliance of products, ingredients, packaging, raw materials, labels, and claims across applicable markets
- Oversee registrations, notifications, approvals, renewals, and amendments for products globally
- Lead regulatory support activities involving agencies and jurisdictions including EPA, FDA, Health Canada, EU, UK, Australia, Mexico, Korea, and other applicable markets
- Direct regulatory review and approval of product claims, marketing materials, specifications, and customer communications
- Provide expertise related to ingredient compliance, substances of concern, PFAS, restricted materials, and emerging chemical regulations
Sustainability & Emerging Regulations
- Lead compliance initiatives related to Extended Producer Responsibility (EPR), packaging regulations, environmental claims, recyclability requirements, and sustainability legislation
- Monitor and interpret evolving global regulatory requirements affecting Rockline products and technologies
- Develop risk mitigation strategies that support both business objectives and compliance requirements
- Partner with Sustainability and Packaging teams to ensure future readiness and competitive advantage
Innovation & Commercial Partnership
- Collaborate with Innovation and Product Development teams to accelerate commercialization of new products and technologies
- Evaluate regulatory pathways for new ingredients, technologies, products, and market opportunities
- Support development of claims strategies and registration plans for new product launches
- Partner with Commercial teams to support customer requirements and market expansion efforts
- Serve as a subject matter expert during regulatory inquiries, customer audits, agency inspections, and legal matters
Industry Leadership & Team Development
- Represent Rockline within industry organizations, trade associations, government agencies, and industry working groups
- Develop regulatory position papers, technical guidance, and communications supporting company interests
- Recruit, coach, mentor, and develop regulatory affairs professionals
- Build organizational capability in regulatory affairs, product stewardship, and compliance
- Establish performance metrics and lead continuous improvement initiatives
- Foster strong cross-functional partnerships throughout the organization
What We're Looking For:
Required
- Bachelor's degree in a scientific field such as Chemistry, Toxicology, Regulatory Affairs, Environmental Science, Biology, Chemical Engineering, Pharmaceutical Sciences.
- 15+ years of progressively responsible Regulatory Affairs experience
- 10+ years of people leadership experience
- Experience working directly with regulatory agencies
- Strong knowledge of global regulatory frameworks and compliance requirements
Preferred
- Advanced degree or professional certification
- Experience with EPA registrations
- Experience supporting international regulatory requirements
- Experience with sustainability and product stewardship programs
Benefits
We offer a comprehensive benefits package designed to support your health, financial security, and work-life balance, including:
Health & Wellness
- Medical, dental, and vision coverage
- Wellness programs
- Fitness reimbursement
Financial Security
- Retirement savings with company match
- Life and disability insurance
- Optional supplemental coverage
Career & Lifestyle
- Paid time off at start
- Education reimbursement
- Employee discount programs
Mental Health Support
- Confidential counseling and resources for personal and work-life needs
Work Environment
- Hybrid/onsite position based in Sheboygan, Wisconsin
- Up to 25% travel annually
- Leadership role with direct people management responsibilities
Join the Rockline Team
At Rockline, you'll find the stability of a successful global manufacturer, the accessibility of a privately held company, and the opportunity to help shape strategic decisions that drive our future.
If you're ready to lead, influence, and make a lasting impact, apply today.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.
See All 8 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
- 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 Oterra, Dr. Comfort, and DataAnnotation, based on current listings on Migrate Mate as of November 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 Sheboygan, Mequon, and Madison. 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 November 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 8 Regulatory Affairs Analyst Jobs in Wisconsin
Find roles in Wisconsin that match your experience and apply in just a few clicks.
Find Jobs