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Location: Remote / Watsonville, CA Salary - 103K - 120K    Regulatory Claims Substantiation Scientist Job Summary: The Regulatory Claims Substantiation Scientist (RCSS) will review and propose revisions to claim substantiations in the form of compiled literature research and scientific writing from the research department. The RCSS will work both independently and collaboratively with members of the Regulatory, Research, Product Development (PD), Marketing, and Education teams. In this capacity, the RCSS will review and propose revisions to the scientific evidence and rationale required to support the nutrition and health-related claims associated with the ingredients of dietary supplement products. This work involves researching topics and preparing, reviewing, revising, and maintaining technical documents. Location Statement: This is a remote position for those who live outside of 40 miles from Nordic Naturals headquarters in Watsonville, CA. Our culture is very important to us and for team members who live inside of the 40-mile radius, we expect them to be onsite occasionally to help support our collaborative community. Reasonable Accommodations Statement: To accomplish this job successfully, an individual must be able to perform, with or without reasonable accommodation, each essential function satisfactorily. Reasonable accommodations may be made to help enable qualified individuals with disabilities to perform the essential functions.  Essential Functions: ● Review of in-depth scientific evidence of the biological effects of ingredients used in Nordic Naturals products. ● Partner with research regulatory functions to ensure compliance to appropriate regulatory requirements. ● Propose revisions to claims substantiations documents to better support a specific health claim within DSHEA and FDA/FTC guidelines. ● Stay abreast of the latest dietary supplement risks from FDA, FTC, and third-party litigation. ● Identify and propose revisions to high-risk claims and/or language within internal claims documents. ● Drive continual self-education primarily through independent study of peer-reviewed scientific literature and recent court decisions impacting the dietary supplement industry. ● Develop expertise in the terminology, biochemistry, molecular biology, physiology, pharmacology and clinical outcomes associated with individual dietary ingredients and associated structure function claims. ● Attendance at scientific, regulatory, and legal conferences and seminars as necessary. ● Review, summarize and/or substantiate the mechanistic and clinical evidence supporting product claims ● Ability to understand and articulate relevant information including molecular mechanisms, biochemical functions, pharmacokinetics, physiological effects, pharmacological and clinical evidence from a range of study types (e.g., observational, interventional, meta-analysis). ● Communicates and collaborates with team members to plan, develop, and produce high-quality communication products in a dynamic environment. ● Manages projects in a timely fashion and adheres to project schedules and deadlines.● Works simultaneously on multiple projects, independently setting work priorities to meet changing deadlines and scope-of-work definitions. ● Performs substantive edits, correcting grammar, technical usage, content, and organizational problems ● Adjusts processes to accommodate changes and resolve issues. ● Collaborate with the PD Team to assess regulatory risk of formulas and improve existing formulas as necessary. ● Maintain working knowledge of new and innovative products and industry trends. Key Contributions in First Year: ● Achieve an understanding of current Nordic Naturals regulatory risk tolerance and cross functional alignment (marketing, legal, research, etc.) on substantiation standards. ● Complete product claims substantiation review for the Nordic Natura