Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Regulatory Affairs Specialist

Better Being

Regulatory Affairs Specialist

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.

The Regulatory Affairs Specialist supports international regulatory compliance and market access activities for food supplements. The position evaluates formulations, labeling, claims, and regulatory requirements across global markets; supports product registrations and notifications; prepares country-specific regulatory documentation; and serves as a regulatory resource for international product development and commercialization initiatives.

Essential Functions

Regulatory Compliance and Market Access

  • Evaluate food supplement formulations for compliance with regulatory requirements in international markets.
  • Research and interpret applicable legislation, guidance documents, and regulatory frameworks.
  • Provide regulatory guidance on ingredients, product claims, formulations, and labeling requirements.
  • Monitor regulatory developments and communicate impacts to internal stakeholders.

Production Registration and Documentation

  • Prepare and maintain regulatory dossiers and supporting documentation for product registrations, notifications, and market access activities.
  • Develop country-specific regulatory documentation to support global product launches.
  • Support registration and notification activities across assigned international markets.
  • Gather, organize, evaluate, and maintain regulatory information from internal and external sources.

Labeling and Claims Review

  • Review product labels and packaging content to ensure compliance with local market requirements.
  • Evaluate marketing and product claims for regulatory compliance and consistency with supporting documentation.
  • Support implementation of required labeling updates resulting from regulatory changes.

Project Management and Collaboration

  • Manage multiple regulatory projects simultaneously while meeting business timelines and market launch objectives.
  • Build and maintain effective relationships with internal teams, customers, consultants, and regulatory authorities.
  • Support continuous improvement of regulatory processes, policies, and systems.
  • Serve as a regulatory resource to Marketing, R&D, Quality, Supply Chain, and Commercial teams.

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 or Master's degree in Food Technology, Food Science, Nutrition, Regulatory Affairs, or a related scientific discipline.
  • Ability to research, interpret and apply international legislation, regulatory guidance, and scientific literature to support regulatory decision-making and product compliance activities.
  • Ability to evaluate food supplement formulations, ingredients, labeling content, and product claims against applicable regulatory requirements across multiple international markets.
  • Ability to prepare, review, and maintain regulatory dossiers, registration files, notifications, and supporting documentation with a high degree of accuracy and attention to detail.
  • Ability to accurately review detailed technical and scientific documentation and identify inconsistencies, omissions, compliance risks, and documentation gaps.
  • Ability to independently prioritize and advance multiple projects with competing deadlines while supporting business and product launch timelines.
  • Strong written and verbal communication skills, including the ability to explain regulatory requirements and recommendations to cross-functional teams, customers, and external stakeholders.
  • Ability to gather, organize, evaluate, and maintain regulatory information from multiple sources and translate findings into practical business guidance.
  • Proficiency with Microsoft Word and Excel and the ability to learn company and industry-specific systems.
  • Fluent in English, both written and spoken, with the ability to communicate effectively with global stakeholders. Additional language capabilities are beneficial when supporting international markets.

Preferred

  • Experience in regulatory affairs, food supplement compliance, product registration, food science, or a related field.
  • Experience supporting food supplement registrations, notifications, or market access activities in international markets.
  • Familiarity with regulatory requirements applicable to the European Union and other international food supplement markets.
  • Experience preparing regulatory dossiers and country-specific registration documentation.
  • Experience working with regulatory databases, document management systems, or product lifecycle 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.

Vacancy posted 3 days ago
Similar jobs that could be interesting for youBased on the Regulatory Affairs Specialist in United States vacancy
  • $42 - $50 per hour

     ...Regulatory Affairs Specialist – Valencia, CA (Occasionally in Burbank)   Company Benefits ~100% employer paid medical and dental  ~401(k) matching contribution ~ Generous PTO and paid holidays ~ Long-term disability ~ Life and AD&D ~ Health Care and Dependent... 
    Suggested
    Hourly pay
    Work at office

    Eckert & Ziegler Isotope Products, Inc.

    Valencia, CA
    1 day ago
  •  ...Regulatory Affairs Specialist II The Regulatory Affairs Specialist II is responsible for the planning and preparation of submissions to obtain regulatory approvals for new and modified medical devices in specific markets. The Regulatory Affairs Specialist II develops... 
    Suggested
    Work at office
    Local area
    Afternoon shift
    Early shift

    Cook Vandergrift

    Vandergrift, PA
    5 days ago
  •  ...and create, through collaboration, cutting edge solutions to tough problems. Job Summary Responsible for supporting Regulatory Affairs, Design Quality Assurance and software compliance activities for Meridian's in vitro diagnostic (IVD) instruments and... 
    Suggested
    Remote work
    Flexible hours

    Meridian Bioscience

    United States
    1 day ago
  •  ...Masimo Regulatory Affairs Specialist Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Masimo, one of Danaher's 15+ operating companies, our work saves lives—and we... 
    Suggested
    Work experience placement
    Local area
    Remote work
    Work from home
    Flexible hours

    Aldevron

    United States
    4 days ago
  • $80.43k - $107.25k

     ...The Regulatory Affairs Specialist II supports global regulatory activities throughout the product lifecycle for medical devices, in vitro diagnostics (IVDs), and life science products. The role develops and executes regulatory strategies, prepares and maintains regulatory... 
    Suggested
    Full time
    Remote work

    CooperCompanies

    Remote
    3 days ago
  •  ...About the Role Our client is seeking an experienced and knowledgeable Regulatory Affairs Specialist to manage regulatory compliance for their pharmaceutical products within the Free State region. This role is pivotal in ensuring that all product development, manufacturing... 
    Remote work
    Flexible hours

    Placements24

    Willows, CA
    12 hours ago
  •  ...Job Title: Regulatory Affairs Specialist Client: Medical Device Manufacturing Company Duration: 12 Months with possible extension Location: Remote Shift: 1st Shift Description Direct or performs coordination and preparation of document... 
    Remote work
    Shift work
    Day shift

    Three Point Solutions

    United States
    3 days ago
  •  ...Excellence (HCE) RDKK/ Growth Mindset: VUCA Managing Change: Teamwork & Collaborations: Achieving Results: Regulatory Affairs Specialist Salary: 300,000 ※ 22,000~ ※ 51,936 (20) Who We Are A healthier future drives us to innovate. Together, more... 
    Remote work

    Roche

    United States
    1 day ago
  •  ...Regulatory Affairs Specialist Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure TM. Everything we do is aligned with this singular purpose. We work... 
    Contract work
    Interim role
    Remote work
    Flexible hours

    Imaging Endpoints

    United States
    3 days ago
  •  ...Regulatory Affairs Specialist NPAworldwide Recruitment Network Location: TOKYO, Tokyo, Japan Remote Status: fully remote Employment Type: Full Time/Direct Hire Compensation: 11000000-13000000 / Japanese Yen / Annual Salary Visa sponsorship provided: Yes... 
    Full time
    Remote work
    Worldwide
    Overseas
    Visa sponsorship
    Free visa

    NPAworldwide

    United States
    4 days ago
  •  ...Regulatory Affairs Specialist Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $35 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating... 
    Remote work

    Human Direct

    United States
    4 days ago
  •  ...for excellence in everything we do. Key Responsibilities Regulatory Compliance & Labeling Support regulatory compliance...  ...experience may be considered. ~2–4 years of experience in regulatory affairs, food manufacturing, or a related field. Recent graduates are... 
    Full time
    Work at office
    Worldwide

    Rana Meal Solutions, LLC

    Bartlett, IL
    12 hours ago
  •  ...wij op zoek naar een nauwkeurige en proactieve collega voor ons Regulatory team. Jouw rol Jij ondersteunt de afdeling bij het...  ...updates van bestaande wetgeving in samenspraak met de Regulatory affairs manager. Jouw profiel Je bent in het bezit van een bachelor... 
    Flexible hours

    Vidara

    Perryville, Perry County, MO
    12 hours ago
  •  .... Skills Functional Competencies Knowledge of Pharmaceutical Life Cycle Process - Level 3 - Influencing Knowledge of Regulatory Requirements & Compliance - Level 3 - Influencing Knowledge of Technology Trends - Level 2 - Demonstrating Project/Program... 
    Full time
    Local area

    Aequor Information Technologies Pvt. Ltd.

    Ridgefield, CT
    12 hours ago
  •  ...Regulatory Affairs Specialist II Fully Remote (within US) | Flexible Hours | 40 hr/week If you are a regulatory professional with 3 to 5 years of experience preparing FDA medical device submissions, and you want your expertise to directly shape how new medical... 
    Full time
    For contractors
    Work at office
    Remote work
    Worldwide
    Flexible hours

    Mittal Consulting

    United States
    3 days ago
  • The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class I and II devices, software as a medical device, and... 

    Cedent Consulting

    Plano, TX
    1 day ago
  • $110k - $150k

     ...font-size: 30px; font-weight: bold; width: 883px; left: 5px; height: 72px; padding-left: 17px; padding-top: 15px; } The Regulatory Affairs Specialist applies regulatory expertise and business knowledge to ensure medical devices are developed, registered, commercialized,... 
    Work experience placement
    Local area
    Immediate start
    Flexible hours

    Coloplast

    Minneapolis, MN
    3 days ago
  •  ...financial flexibility by offering contingent labor as a variable cost.Job DescriptionThis individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing of periodic regulatory reports (i.e. DSURs, orphan annual... 
    Work at office
    Immediate start

    Artech

    Bridgewater, NJ
    3 days ago
  •  ...execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• The Regulatory Affairs Operations (RA Ops) submission group is organized to provide submission development support to project teams and the... 
    Immediate start

    Artech

    Somerville, MA
    1 day ago
  • DescriptionWho We Are Looking ForWe’re looking for a regulatory affairs specialist to join our team and help bring our products to market. In this role, you’ll turn regulatory insights into practical guidance for product development, quality, and marketing, and prepare... 
    Work at office
    Flexible hours

    USANA Health Sciences

    Salt Lake City, UT
    3 days ago
  • Brecksville, OHDescriptionJob Title: Regulatory Affairs SpecialistDepartment: RegulatoryReports To: Director of Regulatory AffairsFLSA Status: ExemptSupervise the work of others: NoPosition Summary:This position is responsible for preparing submissions to various regulatory... 
    Work experience placement
    Work at office

    Applied Medical Technology

    Brecksville, OH
    12 hours ago
  •  ...patient care and creating better patient outcomes.Job Title:Regulatory Affairs SpecialistReports To:Regulatory Affairs ManagerLocation:Austin...  ...HealthWe are looking for an experienced Regulatory Affairs Specialist to join our global Regulatory Affairs team. In this role,... 
    Full time
    Work at office

    Enovis

    Austin, TX
    1 day ago
  •  ...international medical device manufacturer has an exciting career opportunity for a highly talented and well-experienced Regulatory Affairs Specialist with FDA experience who will report directly into the Regulatory Affairs Manager. Essential Functions and Responsibilities... 
    Work experience placement
    Local area

    Nesco Resource

    Melville, NY
    3 days ago
  •  ...provides flexibility to work 4 days on site and Friday remotely on a weekly basis in Covington, GA. *** Job DescriptionThe Regulatory Affairs Specialist II is responsible for implementation of regulatory strategies including domestic and international submissions and other... 
    Full time
    Work at office
    Remote work
    Day shift

    BD, Becton and Dickinson

    Covington, GA
    4 days ago
  •  ...is working in the CMC area. Relevant experience is requiredExperience: 3 to 6 yearsExperience with drug/biologics licensurePrior regulatory experienceTechnical writing experience (CMC experience )Scientific background,Required Skills:CMC/ Regulatory writing experienceScientific... 
    Work at office
    Immediate start

    Artech

    Swiftwater, PA
    1 day ago
  • Overview The Regulatory Affairs Specialist 1 is responsible for the planning and preparation of submissions to obtain regulatory approvals for new and modified Class I, II, III and IV medical devices in specific markets. In addition to submissions, the Regulatory Affairs... 
    H1b
    Work at office
    Local area

    Cook Medical

    Bloomington, IN
    2 days ago
  •  ...both internal and external cross-functional project teams.• The Regulatory CMC Technical Associate may be called upon to author technical...  ...Master s Degree a plus• 4+ years of pharmaceutical regulatory affairs experience• Strong knowledge of NDA, ANDA, MAA, BLA, CTA, or... 
    Work at office
    Local area
    Immediate start

    Artech

    Bridgewater, NJ
    1 day ago
  • The Compliance Specialist reports to the Director Legal, Compliance, Privacy & Security (“Director”) and has a key role in supporting the...  ...basis.Conduct research and develop written communication on regulatory requirements to ensure ongoing updates upon request. Manage compliance... 
    Contract work

    Cedent Consulting

    Houston, TX
    1 day ago
  • The Regulatory Affairs Specialist 3 develops and executes regulatory strategy and integrates regulatory requirements throughout the product lifecycle. Relies on extensive experience and judgment to plan, create, develop and maintain materials needed for regulatory compliance... 

    Cedent Consulting

    Addison, TX
    1 day ago
  • CEDENT is seeking a Regulatory Affairs Specialist in Brecksville, OH to prepare regulatory submissions and maintain compliance for medical devices. You will coordinate with FDA, Notified Bodies, and international partners to ensure timely registrations and documentation... 

    Comunidade Metodista

    Brecksville, OH
    1 day ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Regulatory Affairs Specialist. Be the first to apply!