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Project Manager Biotech Jobs in Brookfield, WI (NOW HIRING)

... biotechnology regulations. As the regulatory leader for North America, this position serves as the ... Develop and implement regulatory strategies to support new product launches, innovation projects ...

New

... biotechnology regulations. As the regulatory leader for North America, this position serves as the ... Develop and implement regulatory strategies to support new product launches, innovation projects ...

Validation Engineer

Hartland, WI ยท On-site

$73K - $110K/yr

... projects and ensure that deadlines and goals are being met. Frequently update management and team ... Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical ...

Validation Engineer

Hartland, WI ยท On-site

$73K - $110K/yr

... projects and ensure that deadlines and goals are being met. Frequently update management and team ... Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical ...

... projects and ensure that deadlines and goals are being met. Frequently update management and team ... Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical ...

Ability to lead projects or workstreams * Ability to manage and prioritize multiple tasks in a fast ... biotech, medical device, or clinical * Experience leading validation deliverables for GxP systems ...

Ability to lead projects or workstreams * Ability to manage and prioritize multiple tasks in a fast ... biotech, medical device, or clinical * Experience leading validation deliverables for GxP systems ...

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Project Manager Biotech information

See Brookfield, WI salary details

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How much do project manager biotech jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for project manager biotech in Brookfield, WI is $43.78, according to ZipRecruiter salary data. Most workers in this role earn between $37.98 and $48.03 per hour, depending on experience, location, and employer.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.
What are popular job titles related to Project Manager Biotech jobs in Brookfield, WI? For Project Manager Biotech jobs in Brookfield, WI, the most frequently searched job titles are:
What job categories do people searching Project Manager Biotech jobs in Brookfield, WI look for? The top searched job categories for Project Manager Biotech jobs in Brookfield, WI are:
What cities near Brookfield, WI are hiring for Project Manager Biotech jobs? Cities near Brookfield, WI with the most Project Manager Biotech job openings:
Infographic showing various Project Manager Biotech job openings in Brookfield, WI as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, 2% Contract, and 1% Nights. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $91,056 per year, or $43.8 per hour.

Regulatory Affairs Manager

Oterra

Mount Pleasant, WI โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


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.