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Director of Science and Regulatory Affairs

Job

Snap Supplements®

Vancouver, WA (In Person)

Full-Time

Posted 1 week ago (Updated 1 day ago) • Actively hiring

Expires 6/23/2026

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Job Description

Director of Science and Regulatory Affairs at Snap Supplements® Director of Science and Regulatory Affairs at Snap Supplements® in Vancouver, Washington Posted in 2 days ago.
Type:
full-time
Job Description:
KEY RESPONSIBILITIES
Scientific & Medical LeadershipDefine Snap's scientific and medical strategy; serve as the primary internal expert on nutrition, physiology, and ingredient scienceEvaluate and synthesize clinical research to substantiate ingredient efficacy, product claims, and safety profilesIdentify and oversee clinical or observational studies; represent the brand with scientific advisors, KOLs, and medical professionalsFormulation & Product DevelopmentDevelop and review science-backed formulas across delivery formats with a focus on efficacy, bioavailability, and ingredient synergyOwn the full formula lifecycle from concept through stability testing and commercial launch; partner with CMOs on scale-up and troubleshootingVet and qualify ingredient suppliers; stay current on emerging ingredients and delivery technologies to guide portfolio innovationRegulatory Affairs & ComplianceEnsure all products, claims, and marketing materials comply with FDA, FTC, DSHEA, and cGMP requirementsBuild and maintain substantiation files, scientific dossiers, and third-party certifications (NSF, Informed Sport, USP)Monitor regulatory developments, advise leadership on risk, and lead responses to AERs or regulatory inquiriesCross-Functional Partnership & EducationCollaborate with Marketing, Product, and Legal teams to ensure scientific accuracy and brand integrity across all channelsDevelop internal training materials and consumer-facing educational content that translate complex science into accessible insightsREQUIREMENTS3+ years of experience in medical affairs, scientific communications, or product development within the supplement or nutraceutical industryDeep knowledge of FDA, FTC, DSHEA, and cGMP regulatory frameworks; proven experience substantiating label and marketing claimsHands-on supplement formulation experience including ingredient sourcing, supplier qualification, and CMO managementStrong ability to evaluate clinical studies and translate findings into product and marketing strategyExcellent communication skills with both scientific and non-scientific audiences; high ethical standards and attention to detailPREFERREDExperience designing or managing clinical trials related to dietary supplements, functional nutrition, or ingredient efficacyFamiliarity with GRAS, NDI, and structure/function claim submissionsRegulatory Affairs Certified (RAC) designation from RAPSExperience working with medical professionals, research consultants, KOLs, or academic institutionsFamiliarity with major retail compliance requirements (Costco, Walmart, GNC, Amazon)Experience in a DTC supplement brand with a high-volume SKU portfolio (50+ products)Equal Opportunity EmployerSnap Supplements is an Equal Opportunity Employer (EOE). We welcome and consider all qualified applicants for employment without regard to race, color, religion, sex, national origin, ancestry, citizenship status, pregnancy, disability, age, military status, marital status, gender identity or expression, sexual orientation, genetic information, or any other protected status in accordance with applicable federal, state, and local laws. recblid c98krldghgx4h3d2qcbnqis0xzppg6

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