Full-Time

Regulatory Claims Substantiation Scientist

Updated on 8/23/2026

Nordic Naturals

Nordic Naturals

Compensation Overview

$103k - $120k/yr

Watsonville, CA, USA

Remote

Remote outside 40 miles of the Watsonville headquarters; employees within 40 miles are expected onsite occasionally.

Bachelor's, Master's, PhD

Category
Legal & Compliance (1)
Required Skills
Microsoft Office
Word/Pages/Docs
Biochemistry
Pharmacology
Excel/Numbers/Sheets
PowerPoint/Keynote/Slides
Requirements
  • A Ph.D. or master's degree in biology, biochemistry, or another life science, or an undergraduate degree in a life science with at least three years of regulatory experience related to claims substantiation in the dietary supplement industry.
  • Knowledge of the nutraceutical industry and its ingredients, including their usage, forms, activities, and relevant characteristics.
  • Applied knowledge and experience with food or supplement regulations, including the Dietary Supplement Health and Education Act, the Federal Food, Drug, and Cosmetic Act, 21 CFR 101, and 21 CFR 111.
  • Experience reading and understanding all sections of scientific and clinical research studies.
  • Familiarity with statistics, clinical-trial design, experimental design, hypothesis testing, and interpretation of laboratory and clinical research data.
  • Ability to read and interpret standard operating procedures and regulations.
  • Fluency in spoken and written English.
  • Skill in scientific writing, comprehension, and presentation of technical information to technical and non-technical audiences.
  • Ability to work independently and cross-functionally, meet deadlines, remain detail-oriented, and prioritize multiple simultaneous tasks.
  • Proficiency with Macintosh OS X, Microsoft Office including Excel, Word, and PowerPoint, Adobe Acrobat, and Google Suite.
Responsibilities
  • Review in-depth scientific evidence concerning the biological effects of ingredients used in company products.
  • Partner with research and regulatory functions to ensure compliance with applicable regulatory requirements.
  • Propose revisions to claims-substantiation documents to support health claims within DSHEA and FDA/FTC guidelines.
  • Monitor dietary-supplement risks identified by the FDA, FTC, and third-party litigation.
  • Identify and propose revisions to high-risk claims and language in internal claims documents.
  • Develop expertise through independent study of peer-reviewed scientific literature and recent court decisions affecting the dietary-supplement industry.
  • Develop expertise in the terminology, biochemistry, molecular biology, physiology, pharmacology, and clinical outcomes associated with dietary ingredients and structure-function claims.
  • Attend scientific, regulatory, and legal conferences and seminars as necessary.
  • Review, summarize, and substantiate mechanistic and clinical evidence supporting product claims.
  • Understand and articulate molecular mechanisms, biochemical functions, pharmacokinetics, physiological effects, and pharmacological and clinical evidence from observational, interventional, and meta-analytic studies.
  • Communicate and collaborate with team members to plan, develop, and produce technical communication products.
  • Manage projects, schedules, deadlines, priorities, and changing scopes of work.
  • Perform substantive edits addressing grammar, technical usage, content, and organizational issues.
  • Adjust processes to accommodate changes and resolve issues.
  • Collaborate with the Product Development team to assess formula regulatory risk and improve existing formulas.
  • Maintain working knowledge of innovative products and industry trends.
  • Complete claims-substantiation reviews for the product portfolio and contribute to regulatory-content knowledge-management practices.
Desired Qualifications
  • Familiarity with EndNote.

Company Size

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Company Stage

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Total Funding

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Headquarters

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Founded

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