... 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 ...
... 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 ...
Regulatory Affairs Manager
Mount Pleasant, WI · On-site
... 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 ...
Regulatory Affairs Manager
Mount Pleasant, WI · On-site
... 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 ...
Senior Validation Engineer
Milwaukee, WI · On-site
... specializing in pharma, biotech, API, Medical Device and laboratory facilities. Compli ... Manage multiple validation projects and priorities while meeting established project milestones and ...
Quick apply
Senior Validation Engineer
Milwaukee, WI · On-site
... specializing in pharma, biotech, API, Medical Device and laboratory facilities. Compli ... Manage multiple validation projects and priorities while meeting established project milestones and ...
Senior Validation Engineer
Milwaukee, WI · On-site
... specializing in pharma, biotech, API, Medical Device and laboratory facilities. Compli ... Manage multiple validation projects and priorities while meeting established project milestones and ...
Senior Validation Engineer
Milwaukee, WI · On-site
... specializing in pharma, biotech, API, Medical Device and laboratory facilities. Compli ... Manage multiple validation projects and priorities while meeting established project milestones and ...
Senior Validation Engineer
Milwaukee, WI · On-site
... specializing in pharma, biotech, API, Medical Device and laboratory facilities. Compli ... Manage multiple validation projects and priorities while meeting established project milestones and ...
Senior Validation Engineer
Milwaukee, WI · On-site
... specializing in pharma, biotech, API, Medical Device and laboratory facilities. Compli ... Manage multiple validation projects and priorities while meeting established project milestones and ...
Senior Validation Engineer
Milwaukee, WI · On-site
... specializing in pharma, biotech, API, Medical Device and laboratory facilities. Compli ... Manage multiple validation projects and priorities while meeting established project milestones and ...
Senior Validation Engineer
Milwaukee, WI · On-site
... specializing in pharma, biotech, API, Medical Device and laboratory facilities. Compli ... Manage multiple validation projects and priorities while meeting established project milestones and ...
Manufacturing Consulting Manager - Life Sciences, Digital CMC / PLM
Milwaukee, WI · On-site
$94K - $293K/yr
The Work: Accenture is seeking a Manager to drive project execution in Digital CMC and PLM ... We work with our pharmaceutical, biotech, medical technology, distributor and consumer health ...
Manufacturing Consulting Manager - Life Sciences, Digital CMC / PLM
Milwaukee, WI · On-site
$94K - $293K/yr
The Work: Accenture is seeking a Manager to drive project execution in Digital CMC and PLM ... We work with our pharmaceutical, biotech, medical technology, distributor and consumer health ...
Strategic Sourcing Manager
$127K - $164K/yr
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project Management Experience - able to lead teams that cut across geographic and functional ...
Strategic Sourcing Manager
$127K - $164K/yr
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project Management Experience - able to lead teams that cut across geographic and functional ...
Quality Assurance Engineer
Franklin, WI · On-site
Project management support and project coordination support * Preparing annual Management Reviews ... Experience in the pharmaceutical, biotech, or food processing industry * Hands-on experience with ...
Quality Assurance Engineer
Franklin, WI · On-site
Project management support and project coordination support * Preparing annual Management Reviews ... Experience in the pharmaceutical, biotech, or food processing industry * Hands-on experience with ...
Quality Assurance Engineer
Franklin, WI · On-site
$70 - $120/hr
Project management support and project coordination support * Preparing annual Management Reviews ... Experience in the pharmaceutical, biotech, or food processing industry * Hands-on experience with ...
Quality Assurance Engineer
Franklin, WI · On-site
$70 - $120/hr
Project management support and project coordination support * Preparing annual Management Reviews ... Experience in the pharmaceutical, biotech, or food processing industry * Hands-on experience with ...
Ability to lead projects or workstreams * Ability to manage and prioritize multiple tasks in a fast ... biotechnology firms to global pharmaceutical companies to medical device companies, to drive ...
Ability to lead projects or workstreams * Ability to manage and prioritize multiple tasks in a fast ... biotechnology firms to global pharmaceutical companies to medical device companies, to drive ...
... biotechnology firms to global big pharma to medical device companies-to drive business value ... personal projects, is a strong plus * 8+ years of experience working on or alongside digital ...
... biotechnology firms to global big pharma to medical device companies-to drive business value ... personal projects, is a strong plus * 8+ years of experience working on or alongside digital ...
... managing people and or leadership experience leading teams, project, programs or directing the allocation of resources * Clinical/medical research experience * 6 years of experience in a biotech ...
... managing people and or leadership experience leading teams, project, programs or directing the allocation of resources * Clinical/medical research experience * 6 years of experience in a biotech ...
Validation Engineer
Hartland, WI · 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 · 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 · On-site
$73K - $110K/yr
... projects and ensure that deadlines and goals are being met. Frequently update management and team ... PREFERRED QUALIFICATIONS Masters of Science in Chemistry, Biology, Biotechnology, Chemical ...
Validation Engineer
Hartland, WI · On-site
$73K - $110K/yr
... projects and ensure that deadlines and goals are being met. Frequently update management and team ... PREFERRED QUALIFICATIONS Masters of Science in Chemistry, Biology, Biotechnology, Chemical ...
Validation Engineer
Hartland, WI · 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 · 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 · 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 · 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 · 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 · 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 ...
Life Sciences MedTech Supply Chain, Management Consultant
Milwaukee, WI · On-site
$70K - $205K/yr
We work with our pharmaceutical, biotech, medical technology, distributor, and consumer health ... Supporting sales origination and project delivery in Med Tech Supply Chain and Manufacturing
Life Sciences MedTech Supply Chain, Management Consultant
Milwaukee, WI · On-site
$70K - $205K/yr
We work with our pharmaceutical, biotech, medical technology, distributor, and consumer health ... Supporting sales origination and project delivery in Med Tech Supply Chain and Manufacturing
Paralegal - Intellectual Property
Milwaukee, WI · On-site +1
Experience with pharmaceutical, life sciences, and/or biotech patent prosecution, such as filing of ... Highly organized, able to prioritize workflow and manage projects. * Ability to perform effectively ...
Paralegal - Intellectual Property
Milwaukee, WI · On-site +1
Experience with pharmaceutical, life sciences, and/or biotech patent prosecution, such as filing of ... Highly organized, able to prioritize workflow and manage projects. * Ability to perform effectively ...
Project Manager Biotech information
See Brookfield, WI salary details
$20.71 - $25.40
4% of jobs
$25.40 - $30.10
8% of jobs
$30.10 - $34.80
3% of jobs
$36.85 is the 25th percentile. Wages below this are outliers.
$34.80 - $39.49
21% of jobs
The median wage is $42.43 / hr.
$39.49 - $44.19
21% of jobs
$47.37 is the 75th percentile. Wages above this are outliers.
$44.19 - $48.89
25% of jobs
$48.89 - $53.58
13% of jobs
$53.58 - $58.28
2% of jobs
$58.28 - $62.97
1% of jobs
$62.97 - $67.67
1% of jobs
$67.67 - $72.37
0% of jobs
$20
$43
$72
How much do project manager biotech jobs pay per hour?
What does a project manager in biotech do?
What are the key skills and qualifications needed to thrive as a project manager in biotech?
How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?
What is the difference between Project Manager Biotech vs Clinical Project Manager?
| Aspect | Project Manager Biotech | Clinical Project Manager |
|---|---|---|
| Credentials | Bachelor's or Master's in Life Sciences, Project Management Certification | Bachelor's or Master's in Life Sciences, Clinical Research Certification |
| Work Environment | Biotech companies, R&D labs, manufacturing | Clinical trial sites, hospitals, pharmaceutical companies |
| Industry Usage | Biotech product development, research projects | Clinical trial management, regulatory compliance |
| Common Search/Comparison | Yes | Yes |
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.
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:

Regulatory Affairs Manager
Mount Pleasant, WI
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 23 days ago
Job 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
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.
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
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.