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Regulatory Affairs Manager Biotech Jobs (NOW HIRING)

... biotechnology regulations. As the regulatory leader for North America, this position serves as the ... The Regulatory Affairs Manager will drive regulatory strategies that enable successful ...

... biotechnology regulations. As the regulatory leader for North America, this position serves as the ... The Regulatory Affairs Manager will drive regulatory strategies that enable successful ...

... biotechnology regulations. As the regulatory leader for North America, this position serves as the ... The Regulatory Affairs Manager will drive regulatory strategies that enable successful ...

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... Regulatory Affairs Manager Location: Onsite - Atlanta, GA Position Summary: The Regulatory Affairs ...

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... Regulatory Affairs Manager Location: Onsite - Atlanta, GA Position Summary: The Regulatory Affairs ...

Minimum of two years' management experience * Experience with Regulatory inspections and successful track record Core Competencies Demonstrates expertise in Regulatory Affairs within the Medical ...

Regulatory Affairs Manager

Chicago, IL · On-site

$120 - $180/hr

Serving leading nutraceutical and pharmaceutical brands, Gnosis harnesses the latest biotechnology ... As our Manager, Regulatory Affairs, you'll be the strategic engine behind our Americas growth ...

Serving leading nutraceutical and pharmaceutical brands, Gnosis harnesses the latest biotechnology ... As our Manager, Regulatory Affairs, you'll be the strategic engine behind our Americas growth ...

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Regulatory Affairs Manager Biotech information

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How much do regulatory affairs manager biotech jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for regulatory affairs manager biotech in the United States is $56.97, according to ZipRecruiter salary data. Most workers in this role earn between $42.07 and $66.59 per hour, depending on experience, location, and employer.

What does a regulatory affairs manager do in the biotech industry?

A Regulatory Affairs Manager in the biotech industry oversees the process of ensuring that biotechnology products comply with all relevant regulations and standards. They work closely with regulatory agencies like the FDA or EMA to obtain approvals for new drugs, devices, or therapies. This role involves preparing and submitting documentation, staying updated on changing regulations, and guiding cross-functional teams to ensure products meet safety and efficacy requirements. Their work is essential for bringing new biotech innovations to market in a compliant manner.

What are the key skills and qualifications needed to thrive as a regulatory affairs manager in the biotech industry, and why are they important?

To thrive as a Regulatory Affairs Manager in biotech, you need in-depth knowledge of regulatory guidelines, scientific principles, and compliance processes, typically supported by a degree in life sciences or a related field. Familiarity with submission management systems, regulatory databases, and certifications such as RAC (Regulatory Affairs Certification) are highly valued. Excellent communication, problem-solving, and project management skills distinguish top professionals in this role. These abilities ensure that biotech products meet all regulatory requirements efficiently, minimizing risk and accelerating product approval timelines.

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

AspectRegulatory Affairs Manager BiotechRegulatory Affairs Specialist Biotech
CredentialsBachelor's or Master’s in Life Sciences, often with certifications like RACBachelor's or Master’s in Life Sciences, often with certifications like RAC
Work EnvironmentLeads teams, manages projects, interacts with regulatory agenciesSupports regulatory submissions, prepares documentation, assists managers
Employer & Industry UsageBiotech companies, pharmaceutical firms, regulatory agenciesBiotech companies, contract research organizations, regulatory consulting firms

The Regulatory Affairs Manager Biotech typically oversees regulatory strategies, manages teams, and interacts with authorities, requiring more experience and leadership skills. In contrast, the Regulatory Affairs Specialist Biotech focuses on supporting documentation and submission processes, often serving as part of a team. Both roles require similar credentials but differ in scope and responsibility.

How does a regulatory affairs manager in biotech typically collaborate with cross-functional teams during product development?

A Regulatory Affairs Manager in biotech plays a crucial role in bridging the gap between regulatory agencies and internal teams such as research & development, clinical, quality assurance, and manufacturing. They guide these teams on regulatory requirements, review documentation for compliance, and coordinate regulatory submissions. Frequent meetings and clear communication are essential, as the manager ensures all stakeholders understand timelines, data requirements, and any changes in regulations, ultimately supporting a smoother pathway to product approval.
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Infographic showing various Regulatory Affairs Manager Biotech job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $118,493 per year, or $57 per hour.

Regulatory Affairs Manager

Oterra

Mount Pleasant, WI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 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.