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Regulatory Affairs Co Jobs (NOW HIRING)

ITW Car Care

Regulatory Affairs Associate

Lakeland, FL · Hybrid

Position Summary The Regulatory Affairs Associate supports the organization's product stewardship ... Internship or co-op experience in regulatory compliance or chemical management may be considered.

Envista

Regulatory Affairs Specialist

Brea, CA · On-site

The Regulatory Affairs Specialist creates, evaluates and completes regulatory tasks related to ... Takes initiative to make a positive difference and win with our customers and co-workers.

Medtronic

Prin Regulatory Affairs Spec

Lafayette, CO · On-site

A Day in the Life The Principal Regulatory Affairs Specialist will play a key role in launching new ... The employee is also required to interact with a computer, and communicate with peers and co ...

Medtronic

Prin Regulatory Affairs Spec

Mansfield, MA · On-site

A Day in the Life The Principal Regulatory Affairs Specialist will play a key role in launching new ... The employee is also required to interact with a computer, and communicate with peers and co ...

Medtronic

Prin Regulatory Affairs Spec

Lafayette, CO · On-site

A Day in the Life The Principal Regulatory Affairs Specialist will play a key role in launching new ... The employee is also required to interact with a computer, and communicate with peers and co ...

Medtronic

Prin Regulatory Affairs Spec

North Haven, CT · On-site

A Day in the Life The Principal Regulatory Affairs Specialist will play a key role in launching new ... The employee is also required to interact with a computer, and communicate with peers and co ...

Medtronic

Prin Regulatory Affairs Spec

Moundsview, MN · On-site

A Day in the Life The Principal Regulatory Affairs Specialist will play a key role in launching new ... The employee is also required to interact with a computer, and communicate with peers and co ...

Medtronic

Prin Regulatory Affairs Spec

Boston, MA · On-site

A Day in the Life The Principal Regulatory Affairs Specialist will play a key role in launching new ... The employee is also required to interact with a computer, and communicate with peers and co ...

Medtronic

Prin Regulatory Affairs Spec

North Haven, CT · On-site

A Day in the Life The Principal Regulatory Affairs Specialist will play a key role in launching new ... The employee is also required to interact with a computer, and communicate with peers and co ...

Medtronic

Prin Regulatory Affairs Spec

Boston, MA · On-site

A Day in the Life The Principal Regulatory Affairs Specialist will play a key role in launching new ... The employee is also required to interact with a computer, and communicate with peers and co ...

Medtronic

Prin Regulatory Affairs Spec

North Haven, CT · On-site

A Day in the Life The Principal Regulatory Affairs Specialist will play a key role in launching new ... The employee is also required to interact with a computer, and communicate with peers and co ...

Medtronic

Prin Regulatory Affairs Spec

Mansfield, MA

A Day in the Life The Principal Regulatory Affairs Specialist will play a key role in launching new ... The employee is also required to interact with a computer, and communicate with peers and co ...

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Regulatory Affairs Co information

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$15

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How much do regulatory affairs co jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for regulatory affairs co in the United States is $34.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $26.20 per hour, depending on experience, location, and employer.

What is a regulatory affairs coordinator?

Regulatory Affairs Coordinators are professionals who help organizations ensure compliance with relevant laws and regulations, particularly in industries such as pharmaceuticals, medical devices, and biotechnology. They assist with the preparation, review, and submission of regulatory documents to agencies like the FDA or EMA. Their work helps to ensure that products meet all necessary requirements for safety, efficacy, and quality before they reach the market. Additionally, they stay updated on regulatory changes and communicate these updates to the appropriate teams within their organization.

What are the key skills and qualifications needed to thrive as a regulatory affairs coordinator?

To thrive as a Regulatory Affairs Coordinator, you need a solid understanding of regulatory guidelines, documentation management, and relevant scientific or healthcare background, often supported by a degree in life sciences or a related field. Familiarity with regulatory submission systems, document tracking tools, and knowledge of FDA, EMA, or other regulatory agency requirements is typically required. Exceptional attention to detail, organizational skills, and effective communication are vital soft skills for this position. These skills ensure accurate and timely submissions, maintain compliance, and facilitate smooth interactions with regulatory agencies, which are crucial for product approvals and business success.

What are some common challenges faced by regulatory affairs professionals when working with cross-functional teams?

Regulatory Affairs professionals often collaborate with departments such as R&D, quality assurance, and marketing to ensure products meet all compliance requirements. A common challenge is balancing the need for regulatory compliance with the business objectives and timelines of other teams. Effective communication is essential, as regulatory requirements can be complex and may require negotiation or compromise to align with project goals. Building strong relationships and maintaining up-to-date knowledge of regulations helps Regulatory Affairs professionals successfully guide teams through the compliance process.

What is the difference between Regulatory Affairs Co vs Quality Assurance Specialist?

AspectRegulatory Affairs CoQuality Assurance Specialist
CredentialsRegulatory Affairs Certification (RAC), degrees in life sciences or pharmacyISO auditor certifications, degrees in quality management or related fields
Work EnvironmentRegulatory agencies, pharmaceutical or biotech companies, compliance departmentsManufacturing plants, labs, quality control departments
Industry UsageEnsures compliance with regulations, prepares submissionsMaintains product quality, audits processes, implements quality systems

While both roles focus on compliance and quality, Regulatory Affairs Co primarily manages regulatory submissions and compliance with government agencies, whereas Quality Assurance Specialists focus on maintaining product quality through audits and process improvements. Both roles are essential in the life sciences industry and often collaborate to ensure products meet standards and regulations.

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Regulatory Affairs Co jobs near you
Infographic showing various Regulatory Affairs Co job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 8% Part Time, and 3% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $71,960 per year, or $34.6 per hour.

Regulatory Affairs Scientist

Salt Lake City, UT • On-site

Better Being Co
Manufacturing • 1 - 5K employees

8.7

Company rating: 8.7 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

Good employer

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Learn more about Better Being Coexternal

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 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 that'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 Functions
Third-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 - specifications, certificates of analysis, allergen and GMO statements, country of origin, and regulatory status - 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 escalate 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
  • Bachelor'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 cross-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 industry-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 third-party certification programs such as USDA Organic, Non-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 well-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 work-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 well-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.

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