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Gmo Project Manager Jobs (NOW HIRING)

Regulatory Manager

Hicksville, NY ยท On-site

$125K - $175K/yr

Knowledge of Non-GMO Project Verified requirements is a plus * Canadian food labeling experience is a plus * Excellent analytical, organizational, proofreading, and time management skills

Company Profile Founded in 1977, GMO is a global investment manager committed to delivering ... Complete complex analytical projects * Interpret company announcements and their investment ...

... Management systems and tools. * Coordinate third-party certification programs and maintenance activities for Kosher, Organic, Non-GMO Project, Gluten Free, and other certifications. * Track ...

Desktop Engineer

Boston, MA ยท On-site

$100K - $125K/yr

Company Profile Founded in 1977, GMO is a global investment manager committed to delivering ... focused project work and productivity enhancements. We value individuals who are reliable ...

Marketing Reporting Associate

Boston, MA ยท On-site

$80 - $100/hr

Company Profile Founded in 1977, GMO is a global investment manager committed to delivering ... Contributing to projects to advance the strategic objectives of GMO's Marketing and Client Services ...

2027 Investment Research Associate

Boston, MA ยท On-site

$100K - $125K/yr

Company Profile Founded in 1977, GMO is a global investment manager committed to delivering ... projects โ€ข Interpret company announcements and their investment implications โ€ข Investigating ...

Sr. Specialist, Regulatory

Chicago, IL ยท On-site

$80K - $112K/yr

FDA formulation and labeling requirements to navigate complexity, manage risk, and support cross ... Strong knowledge of Kosher, Non-GMO project Verified, Gluten-Free Certified, and USDA Organic ...

Company Profile Founded in 1977, GMO is a global investment manager committed to delivering ... projects Interpret company announcements and their investment implications Investigating ...

Emerging Country Debt Analyst

Boston, MA ยท On-site

$175K - $225K/yr

Company Profile Founded in 1977, GMO is a global investment manager committed to delivering ... projects and set priorities. The ideal candidate will also show a desire for achievement and ...

Company Profile Founded in 1977, GMO is a global investment manager committed to delivering ... Complete complex analytical projects * Interpret company announcements and their investment ...

Emerging Country Debt Analyst

Boston, MA ยท On-site

$175K - $225K/yr

Company Profile Founded in 1977, GMO is a global investment manager committed to delivering ... projects and set priorities. The ideal candidate will also show a desire for achievement and ...

$80 - $100/hr

Company Profile Founded in 1977, GMO is a global investment manager committed to delivering ... Contributing to projects to advance the strategic objectives of GMO's Marketing and Client Services ...

Showing results 21-40

Gmo Project Manager information

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$46

$76

How much do gmo project manager jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for gmo project manager in the United States is $46.24, according to ZipRecruiter salary data. Most workers in this role earn between $40.14 and $50.72 per hour, depending on experience, location, and employer.

What is the difference between Gmo Project Manager vs Gmo Coordinator?

AspectGmo Project ManagerGmo Coordinator
CredentialsBachelor's degree, PMP or similar certification often preferredAssociate's or Bachelor's degree, relevant certifications optional
Work EnvironmentLeads projects, manages teams, oversees budgetsSupports project tasks, coordinates activities, assists managers
Employer & Industry UsageUsed in biotech, agriculture, and food industries for GMO projectsCommonly found in similar industries, supporting GMO initiatives

The Gmo Project Manager typically oversees GMO projects, manages teams, and handles budgets, requiring more experience and certifications. The Gmo Coordinator supports project activities, assists managers, and has a more entry-level role. Both roles are essential in GMO-related industries but differ in responsibilities and seniority.

What are popular job titles related to Gmo Project Manager jobs?

For Gmo Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Gmo Project Manager job openings in the United States as of September 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $96,184 per year, or $46.2 per hour.

Regulatory Affairs Scientist

Salt Lake City, UT โ€ข On-site

$80 - $100/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 8 days ago


Job description

About Us

At Better Being Co. we empower and inspire individuals to feel better and live healthier lives by providing the most trustworthy, pure, and innovative natural wellness solutions. If you thrive in a challenging work environment, surrounded by incredible team members who will help you grow and do your best work, Better Being is the right place for you. Come build with us and be part of an award-winning company thatโ€™s helping create meaningful and lasting change in the healthcare industry.

Job Summary

The Regulatory Affairs Scientist reviews dietary supplements, cosmetic, and beverage labels and formulas for compliance; creates and maintains ingredient specifications; and coordinates third-party certification programs, including organic, non-GMO, and Halal. The position manages assigned regulatory projects through completion and applies foundational chemistry and mathematical concepts when reviewing formulas, specifications, and product labeling.

Essential FunctionsThird-Party Certifications

Coordinate third-party certification programs including USDA Organic, Non-GMO Project Verified, and Halal, and support additional programs such as Kosher, gluten-free, and vegan as the portfolio requires. Prepare and submit certification applications, annual renewals, and product addition requests; assemble supporting documentation and respond to certifier questions and audit findings. Track certification status across the product portfolio and flag expirations, gaps, and at-risk items before they affect production or retail listings.

Label and Formula Review

Review dietary supplement, cosmetic, and beverage labels for regulatory compliance and internal accuracy, including required panels, ingredient declarations, allergen statements, net quantity statements, and product claims. Review formulations for ingredient eligibility, applicable restrictions, permitted use levels, labeling implications, and third-party certification requirements. Verify that marketing claims are consistent with the supporting substantiation on file and appropriately qualified. Coordinate label review and revision cycles and verify that approved changes are incorporated into the final label.

Ingredient and Product Specifications

Create, review, and maintain ingredient and finished product specifications, ensuring identity, grade, source, and quality parameters are accurately captured and kept current. Evaluate incoming ingredient documentation โ€” specifications, certificates of analysis, allergen and GMO statements, country of origin, and regulatory status โ€” against internal requirements and applicable regulations. Request, track, and follow up on required documentation from suppliers, contract manufacturers, government agencies, and certifying bodies until files are complete.

Project Management and Collaboration

Manage multiple concurrent projects against launch timelines, keeping stakeholders informed of status, risks, and dependencies. Identify documentation gaps and potential compliance issues independently, recommend appropriate next steps, and elevate issues when additional review or guidance is needed. Serve as a regulatory resource to Marketing, R&D, Quality, Supply Chain, and Customer Service. Monitor regulatory developments relevant to dietary supplements, cosmetics, and beverages and support implementation of required changes.

Other duties as assigned.

Additional Responsibilities Support of and involvement in company, department, and/or safety policies, procedures, programs and activities. Maintenance of a clean and orderly work area.

Job Qualifications

Required Bachelorโ€™s degree in chemistry, biochemistry, biology, food science, nutrition, or a closely related scientific discipline. Up to 3 years of relevant experience in regulatory affairs, quality assurance, product compliance, food science, or a related field. Working understanding of basic chemistry principles, including compound identity, concentration, purity, and the difference between an ingredient and its active constituents. Ability to perform and verify calculations involving unit conversions (mcg, mg, IU), percent composition, overage calculations, percent Daily Value, and label rounding rules. Ability to accurately review detailed technical documents and identify inconsistencies, omissions, and errors. Ability to independently prioritize and advance multiple projects with competing deadlines. Clear written and verbal communication, including the ability to present findings and recommendations to crossโ€‘functional partners and to correspond professionally with external suppliers and certifying bodies. Proficiency with Microsoft Word and Excel and the ability to learn company and industryโ€‘specific systems. Ability to read, interpret, and apply regulatory text, scientific literature, and technical documentation. Preferred Coursework, internship, or work experience in regulatory affairs, quality assurance, or a related compliance function. Familiarity with laws, regulations, or guidance applicable to dietary supplements, cosmetics, food labeling, advertising claims, or consumer product warnings, such as DSHEA, 21 CFR Part 101 (labeling), 21 CFR Part 111 (dietary supplement cGMP), MoCRA and cosmetic labeling requirements, FTC advertising substantiation standards, or California Proposition 65. Prior exposure to thirdโ€‘party certification programs such as USDA Organic, Nonโ€‘GMO Project, Halal, or Kosher. Experience with specification management, PLM, ERP, or label management systems.

Physical Requirements

While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands to touch, handle, or feel; reach with hands and arms; and talk or hear. The employee must exert up to 20 lbs. of force occasionally, and/or up to 10 lbs. of force frequently, and/or a negligible amount of force to move objects. Specific vision abilities required by this job include near acuity, far acuity, depth perception, accommodation, color vision, and field of vision.

Our Benefits

Join our team and enjoy a comprehensive package of competitive benefits and perks designed to support your wellโ€‘being and professional growth. Our offerings include:

  • Access to our Employee Health Clinic for your medical needs.
  • Comprehensive Medical, Dental, and Vision Insurance coverage.
  • Participation in our Family First Program, emphasizing workโ€‘life balance.
  • 401(K) plan with generous employer match to help you plan for the future.
  • Educational Reimbursement opportunities to support your continued learning and development.
  • Wellness Incentives to promote a healthy lifestyle.
  • Substantial product discounts, because we value our team members as customers too.
  • Generous Paid Time Off and Paid Holidays, ensuring you have time to rest and recharge.

For more information, check out our website Better Being Careers and join us in experiencing a workplace where your wellโ€‘being and success are our top priorities.

This description is not intended to be an exhaustive list of responsibilities and qualifications. The position, duties, and qualifications are subject to change at any time.

We provide equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

At Better Being we empower and inspire individuals to feel better and live healthier lives by providing the most trustworthy, pure, and innovative natural wellness solutions. If you thrive in a challenging work environment, surrounded by incredible team members who will help you grow and do your best work, Better Being is the right place for you. Come build with us and be part of an awardโ€‘winning company thatโ€™s helping create meaningful and lasting change in the healthcare industry.

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