Regulatory Affairs Specialist

Regulatory Affairs Specialist (Utah, USA)The Juice Plus+ Company is a multimillion-dollar competitor in the health and wellness industry, using a unique combination of direct sales and e-commerce to market our plant-based nutritional products in pursuit of our mission to “Inspire Healthy Living Around the World.”Owing to change we are currently recruiting for the role of Specialist, North America Regulatory Affairs, within our Global Regulatory Affairs team. Reporting directly to the Director of Global Regulatory Affairs this role will serve as the primary regulatory point of contact for the US market, managing end-to-end product compliance projects across our food and dietary supplement portfolio. This is a high impact role that sits at the intersection of science, compliance, and storytelling, helping our teams bring compliant, innovative products to market, while helping craft engaging, legally sound content, for US consumers.Your Day to DayLead regulatory assessment of new and reformulated food and dietary supplement products, including ingredient acceptability, claim substantiation, and labeling compliance under FDA regulations (21 CFR, DSHEA, FD&C Act).Evaluate proposed raw materials and novel ingredients for regulatory acceptability; prepare or review NDI notifications as required.Develop and review mandatory label elements including Supplement Facts panels, Nutrition Facts panels, ingredient declarations, warnings, etc.Evaluate the need for NDI notifications for novel ingredients; prepare, file, and maintain NDI notification dossiers in accordance with 21 CFR 190.Review and substantiate structure/function claims in accordance with 21 CFR 101.93 and FTC guidance; prepare and maintain FDA notification files.Partner with the Marketing & Digital team to develop product content, including website copy, social media, and promotional materials that are scientifically credible, consumer-relevant, and compliant with FDA and FTC regulations.Continuously monitor FDA, FTC, and other relevant regulatory bodies (e.g., NPA, AHPA, CRN) for proposed rulemakings, guidance documents, enforcement trends, and legislative developments affecting the US food and dietary supplement industryYou will bringc.3-5 years hands-on regulatory affairs experience in the US food and dietary supplement industryBachelor's degree in Life Sciences, Food Science, Nutrition, Chemistry, or a closely related field.Demonstrated expertise in FDA regulations governing dietary supplements (DSHEA, 21 CFR Parts 101, 111, 190) and conventional foods (21 CFR Part 101).Experience filing structure/function claim notifications and NDI notifications.Experience reviewing and creating compliant product labeling (Supplement Facts, Nutrition Facts, ingredient statements, etc.).Exceptional written and verbal communication skills; ability to translate complex regulatory requirements into clear, actionable guidance for non-technical stakeholders.