1

Regulatory Labeling Manager Jobs in Wisconsin (NOW HIRING)

Provide regulatory guidance on ingredient declarations, color labeling requirements, claims ... Manage and develop the North American Regulatory Affairs team. * Partner closely with Innovation ...

... regulatory documentation. This role will manage day-to-day technical tasks that accelerate ... regulatory labeling · Experience with Genesis or similar nutritional software · Strong ...

This position will assist the Regulatory Manager in reviewing and updating label copies and specifications to ensure that all information is accurate, meets customer requirements, and complies with ...

This position will assist the Regulatory Manager in reviewing and updating label copies and specifications to ensure that all information is accurate, meets customer requirements, and complies with ...

next page

Showing results 1-20

Regulatory Labeling Manager information

See Wisconsin salary details

$29

$57

$87

How much do regulatory labeling manager jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for regulatory labeling manager in Wisconsin is $57.50, according to ZipRecruiter salary data. Most workers in this role earn between $42.45 and $67.21 per hour, depending on experience, location, and employer.

What does a Regulatory Labeling Manager do?

A Regulatory Labeling Manager oversees the development, review, and approval of product labels and packaging to ensure compliance with all relevant regulations and guidelines. They coordinate with various departments, such as regulatory affairs, legal, marketing, and product development, to ensure that all labeling information is accurate and aligns with local and international laws. Their responsibilities often include managing labeling submissions to regulatory authorities, monitoring regulatory changes, and updating labels accordingly to maintain compliance.

How does a Regulatory Labeling Manager typically collaborate with cross-functional teams during the product development process?

As a Regulatory Labeling Manager, you will regularly collaborate with cross-functional teams including regulatory affairs, medical, legal, marketing, and product development. Your role involves ensuring that product labels meet both regulatory requirements and company standards by gathering input from these teams and facilitating consensus on label content. You’ll often lead meetings to align stakeholders, review draft labeling, and coordinate responses to regulatory authority feedback, making strong communication and project management skills essential. This collaborative environment also provides opportunities to broaden your expertise and visibility within the company, supporting long-term career growth.

What are the key skills and qualifications needed to thrive as a Regulatory Labeling Manager, and why are they important?

To thrive as a Regulatory Labeling Manager, you need expertise in regulatory compliance, labeling requirements, and scientific documentation, often supported by a degree in life sciences or a related field. Familiarity with regulatory submission systems, document management tools, and global labeling databases is typically required. Strong attention to detail, project management, and effective cross-functional communication skills set top performers apart in this role. These skills are crucial for ensuring accurate, compliant labeling that meets health authority standards and supports product success in global markets.

What is the difference between Regulatory Labeling Manager vs Regulatory Affairs Specialist?

AspectRegulatory Labeling ManagerRegulatory Affairs Specialist
CertificationsRegulatory Affairs Certification (RAC), FDA certificationsRAC, FDA certifications
Work EnvironmentLeading labeling projects, cross-functional teamsSupporting regulatory submissions, research
Employer & Industry UsagePharmaceuticals, medical devices, biotechPharmaceuticals, medical devices, biotech

The Regulatory Labeling Manager focuses on developing, reviewing, and maintaining product labeling to ensure compliance with regulations. In contrast, the Regulatory Affairs Specialist handles broader regulatory submissions and compliance tasks. Both roles require similar certifications and are common in the same industries, but the Labeling Manager has a more specialized focus on labeling strategies and documentation.

What are the most commonly searched types of Regulatory Labeling jobs in Wisconsin?

The most popular types of Regulatory Labeling jobs in Wisconsin are:

What are popular job titles related to Regulatory Labeling Manager jobs in Wisconsin?

For Regulatory Labeling Manager jobs in Wisconsin, the most frequently searched job titles are:

Infographic showing various Regulatory Labeling Manager job openings in Wisconsin as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $119,601 per year, or $57.5 per hour.

Regulatory Affairs Manager

Mount Pleasant, WI

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago


Job description

Company Description

Oterra is the global leader in naturally sourced colors for food, beverages, dietary supplements, and pet food. With over 140 years of expertise, we believe nature got it right the first time. Join our fast-growing, international team and help us make natural, healthy food accessible worldwide.

Job Description

Job Description

The Regulatory Affairs Manager is responsible for leading regulatory compliance activities for Oterra's portfolio of natural colors across the United States and Canada. This role provides strategic regulatory leadership to support business growth, innovation, customer conversions from synthetic dyes to natural colors, and market expansion while ensuring compliance with all applicable food, beverage, pet food, nutraceutical, and biotechnology regulations.

As the regulatory leader for North America, this position serves as the primary regulatory expert for natural colors and coloring ingredients, partnering closely with Commercial, Innovation, Product Development, Applications, Quality, Operations, and Global Regulatory teams. The Regulatory Affairs Manager will drive regulatory strategies that enable successful commercialization of new color technologies, support customer reformulation initiatives, and influence industry regulatory developments impacting the color industry.

Key Responsibilities

Regulatory Compliance & Strategy

  • Lead and oversee regulatory compliance for Oterra's portfolio of natural colors, marketed in the United States and Canada.
  • Develop and implement regulatory strategies to support new product launches, innovation projects, and customer conversion programs from synthetic colors to natural alternatives.
  • Monitor, interpret, and communicate changes to FDA, USDA, Health Canada, CFIA, California, and other applicable regulations affecting food colors and ingredients.
  • Evaluate regulatory risks and opportunities associated with emerging color technologies, fermentation-derived pigments, and biotechnology solutions.
  • Support the development and commercialization of new pigments and color solutions through regulatory assessments and approvals.

Industry Advocacy & Regulatory Leadership

  • Serve as Oterra's primary representative within industry associations including NATCOL, IACM, and other relevant organizations.
  • Build relationships with regulatory authorities including FDA, USDA, Health Canada, and industry stakeholders.
  • Lead regulatory submissions, color additive petitions, GRAS assessments, certifications, registrations, and regulatory dossiers as required.
  • Partner with Global Regulatory Affairs to support international approvals and harmonization efforts.
  • Monitor legislative and regulatory developments impacting the food color industry and develop proactive business strategies.

Customer & Commercial Support

  • Act as the regulatory expert supporting customer conversions from synthetic dyes to natural colors across food, beverage, confectionery, dairy, bakery, snacks, and pet food applications.
  • Provide regulatory guidance on ingredient declarations, color labeling requirements, claims substantiation, certifications, and market-specific compliance requirements.
  • Support key customer accounts by responding to complex regulatory inquiries and participating in customer meetings as needed.
  • Collaborate with Sales and Marketing teams to identify regulatory opportunities that support business growth and competitive differentiation.

Cross-Functional Leadership

  • Manage and develop the North American Regulatory Affairs team.
  • Partner closely with Innovation, Product Development, Applications, Quality Assurance, Quality Control, Supply Chain, and Operations teams.
  • Support Innovation projects by providing regulatory guidance on new raw materials, pigments, formulations, and technologies.
  • Train internal teams on regulatory requirements, industry trends, and food color regulations.
  • Establish departmental priorities, objectives, and performance metrics aligned with business goals.
Qualifications

Minimum Requirements

  • Bachelor's degree in Food Science, Regulatory Science, Chemistry, Biochemistry, Nutrition, Food Safety, or related scientific discipline.
  • 10+ years of regulatory affairs experience within the food ingredient, food color, flavor, nutraceutical, or specialty ingredient industry.
  • Strong knowledge of FDA color additive regulations, food ingredient regulations, labeling requirements, and Health Canada regulations.
  • Demonstrated expertise in natural colors, coloring foodstuffs, botanical extracts, or specialty food ingredients.
  • Experience supporting customer compliance, product commercialization, and regulatory submissions.
  • Proven ability to influence cross-functional teams and drive regulatory strategy.
  • Strong project management, communication, and leadership skills.

Preferred Qualifications

  • Master's degree in Food Science, Regulatory Science, Chemistry, Biochemistry, or related field.
  • Regulatory Affairs Certification (RAC) or equivalent professional certification.
  • Previous people management experience.
  • Experience with color additive petitions, GRAS notifications, novel ingredient approvals, or international food ingredient regulations.
  • Active participation in NATCOL, IACM, IFT, or other food ingredient industry organizations.
  • Experience supporting synthetic-to-natural color conversion initiatives.

Key Competencies

  • Deep Regulatory Knowledge of Food Colors and Ingredients
  • Strategic Regulatory Leadership
  • Customer-Focused Mindset
  • Industry Advocacy & Networking
  • Regulatory Risk Assessment
  • Cross-Functional Collaboration
  • Team Development & Leadership
  • Project Management
  • Strong Communication & Influencing Skills
  • Innovation & Commercialization Support

Additional Information

What We Offer
At Oterra, we take care of our people – because when you’re supported, you can do your best work. Our benefits are designed to support your health, your future and your life outside of work:

  • Health & Well-being: Comprehensive medical, dental, and vision coverage, plus life and disability insurance.
  • Financial Security: A retirement savings program with 401(k), company match, and bonus program.
  • Time for You: Paid holidays, vacation time, and personal/sick days each year.
  • Engagement in the Workplace: Monthly employee engagement events and team celebrations
  • Growth & Empowerment: A collaborative culture that encourages career growth and professional development opportunities

Equal Employment Opportunity Statement

  • Oterra is an Equal Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex/gender, sexual orientation, gender identity, pregnancy, age, ancestry, national origin, genetic information, marital status, citizenship status (unless required by the applicable law or government contract), disability or protected veteran status or any other status or characteristic protected by law. Oterra is committed to a diverse and inclusive workforce. We are committed to building a team that represents diverse and inclusive backgrounds, perspectives, and skills. Oterra will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen.