Regulatory Affairs Analyst Jobs in Utah
Regulatory affairs analyst jobs in Utah are concentrated in Salt Lake City, Provo, and Ogden, where the state's medical device, pharmaceutical, and life sciences sectors drive consistent demand across seniority levels from entry-level associate to senior principal. Employers such as Merit Medical Systems, 3M Health Care, and Intermountain Health have established regulatory functions in Utah and hire across FDA submissions, quality compliance, and labeling review. The market is among the more active in the Mountain West for this specialty. Find a role that fits below and apply directly.
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Company Overview:
Momentous is a dynamic, fast-growing human performance company offering the highest quality supplements designed to enhance physical and cognitive well-being. At Momentous, we believe that people at their best will produce a positive impact in their personal lives, communities, and, ultimately, the world. No matter our customer's goal or what they want to achieve, we are on a relentless quest to help them get there. We work with some of the greatest minds in science and athletic performance who tap into the latest research and real-world experience to create a portfolio of products designed with one common goal—to help our customers be their best.
What we’re proud of:
- Best in the field. We have built an advanced network of world-renowned experts in the field of human performance.
- Trusted and used by the best. We are honored to work with more than 150 teams in professional and NCAA sports, including Stanley Cup Champions, Tour de France winners, and all NFL Teams.
- Push what’s possible. Named to the prestigious Inc. 5000 list three years in a row (#392 in 2025) as one of the fastest-growing companies in the US. Ranked #4 in the Rocky Mountain Region in 2025.
Position Summary:
Reporting into the VP of Innovation, the Director of Regulatory Affairs is responsible for ensuring that Momentous's entire product portfolio — formulations, labels, marketing claims, and manufacturing practices — complies with FDA, FTC, USDA (where applicable), and international regulatory requirements across all markets where Momentous sells.
This role is the company's primary regulatory authority: setting the standards that Product, Applied Science, Marketing, and Operations build against, evaluating new ingredients and formulations for regulatory viability before they reach commercialization, and serving as Momentous's point of contact for regulatory bodies, co-manufacturers, and legal counsel on compliance matters. The ideal candidate combines deep expertise in dietary supplement law (DSHEA, NDI notifications, GMP) with the judgment to balance rigorous compliance against the pace of a fast-growing consumer brand.
Responsibilities:
Regulatory Strategy & Compliance
- Own Momentous's regulatory compliance strategy across all product categories and all markets (U.S., and international markets as the company expands).
- Evaluate new ingredients, formulations, and delivery formats for regulatory viability early in development — including NDI (New Dietary Ingredient) status, GRAS considerations, and any FDA warning letters or import alerts relevant to a given ingredient.
- Maintain and continuously update Momentous's regulatory framework as FDA, FTC, and state-level guidance evolves (e.g., NDI reform, state-level supplement restrictions, international market access rules).
- Lead regulatory due diligence for new product launches, formulation changes, and market expansions.
Label & Claims Review
- Review and approve all product labels, packaging, and inserts for compliance with FDA labeling regulations (21 CFR Part 101), including nutrient content claims, structure/function claims, and required disclosures.
- Partner with Science Integration, Marketing, and Legal to review consumer-facing claims (website, packaging, advertising, influencer/affiliate content) for substantiation and FTC compliance prior to publication.
- Maintain claims substantiation files for all structure/function and health-related claims across the portfolio.
- Advise on acceptable claims language for new product launches and campaigns, flagging risk before content goes live rather than after.
Manufacturing & Quality Compliance
- Partner with Quality and contract manufacturers/co-packers to ensure GMP compliance (21 CFR Part 111) across the supply chain.
- Support audit readiness for FDA inspections, NSF/Informed Sport certifications, and third-party quality audits.
- Review Certificates of Analysis, supplier documentation, and specification sheets for regulatory adequacy (an area directly relevant to Momentous's ingredient sourcing and finished-product specs) including but not limited to TLA, MSSA, and other supplier contracts.
Cross-Functional Partnership
- Serve as the regulatory voice in Innovation Phase Gate reviews, flagging risk and required documentation early in the product development cycle.
- Train and enable Marketing, Retail, Ecommerce, and Customer Experience teams on regulatory guardrails so they can operate confidently within compliant boundaries.
- Act as primary liaison with outside regulatory counsel, testing labs (e.g., Eurofins, NSF), and industry bodies (e.g., CRN, AHPA) on matters affecting Momentous's category.
- Monitor competitor and industry regulatory actions (warning letters, FTC settlements, recalls) for relevant lessons and risk signals.
International Expansion Support
- Assess regulatory requirements for new international markets (e.g., Canada's NHP framework, EU Regulation 1169/2011, Australia/New Zealand Food Standards Code) as Momentous expands distribution.
- Coordinate labeling and claims adaptation for cross-border sales, including allergen labeling differences already relevant to Momentous's fish oil and other allergen-containing products.
Qualifications:
Required:
- 10+ years of experience in regulatory affairs within dietary supplements, food, pharmaceuticals, or consumer health products, with at least 5 years in a senior or leadership capacity.
- Deep working knowledge of DSHEA, FDA labeling regulations (21 CFR 101, 111), FTC advertising guidance, and NDI notification processes.
- Demonstrated experience reviewing and approving product claims, labels, and marketing content for regulatory compliance.
- Experience working directly with FDA, state regulators, or through FDA inspections/audits.
- Strong cross-functional communication skills — able to translate regulatory requirements into clear guidance for non-regulatory teams (Marketing, Product, Ecommerce).
- Bachelor's degree in a related scientific, legal, or regulatory field; JD, advanced regulatory certification (RAC), or relevant graduate degree a plus.
Preferred:
- Direct experience in sports nutrition, performance supplements, or NSF Certified for Sport / Informed Sport certification processes.
- Experience supporting international market expansion and cross-border regulatory compliance.
- Familiarity with contract manufacturing relationships and GMP audit processes.
- Prior experience at a high-growth consumer brand balancing compliance rigor with commercial speed.
Benefits:
- Our fast-paced, high growth environment creates a strong opportunity for professional development born from evolving experiences
- Competitive cash compensation plus employee stock options
- Health/Vision/Dental
- 401k Match
- Unlimited PTO
- Finish Line Fridays - finish at 3:00 every Friday
- Generous set of observed holidays (18 days of office closure in 2026)
- $1,000 annual perks program to support a high-performance lifestyle
- Access to Momentous products and merchandise
Location:
This is a hybrid role based out of our Park City headquarters.
EQUAL EMPLOYMENT OPPORTUNITY
Momentous provides 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. We are committed to bringing together individuals from different backgrounds and perspectives, and providing employees with a safe and welcoming work environment where everyone can thrive. 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.
See All 5 Regulatory Affairs Analyst Jobs in Utah
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Find JobsRegulatory Affairs Analyst Jobs by City in Utah
Where Utah roles are concentrated, by current openings.
Regulatory Affairs Analyst Job Market in Utah
A snapshot from current Utah openings, updated as new roles post.
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Top Industries Hiring
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- Healthcare & Medical Services
What Utah Employers Look For
The qualifications that appear most often in regulatory affairs analyst jobs across Utah.
- Bachelor's degree in life sciences, engineering, chemistry, or a related technical field
- Working knowledge of FDA regulations including 21 CFR and medical device or drug submission processes
- Experience preparing or supporting regulatory submissions such as 510(k), PMA, or NDA filings
- Familiarity with quality management systems and ISO 13485 or ISO 9001 standards
- Strong written communication skills for preparing regulatory documentation and correspondence
- Regulatory Affairs Certification (RAC) from RAPS preferred or actively pursued by candidates
Regulatory Affairs Analyst Jobs in Utah: Frequently Asked Questions
How do you become a regulatory affairs analyst in Utah?
Most regulatory affairs analysts in Utah enter the field with a bachelor's degree in a life science, engineering, or health-related discipline, then gain hands-on experience in quality assurance, clinical operations, or manufacturing before transitioning into regulatory roles. Utah does not require a state-issued license for this position, but the Regulatory Affairs Certification (RAC) awarded by the Regulatory Affairs Professionals Society is widely recognized by Utah employers and strengthens applications considerably.
Which companies hire regulatory affairs analysts in Utah?
Companies currently hiring regulatory affairs analysts in Utah include Lifewave, Rippling, and Momentous, per current listings on Migrate Mate as of September 2026. Utah's concentration of medical device and diagnostics manufacturers along the Wasatch Front means regulatory openings appear consistently at both large multinationals with Utah operations and homegrown life sciences companies.
Which Utah cities have the most regulatory affairs analyst jobs?
Salt Lake City, Draper, and Bluffdale account for the largest share of regulatory affairs analyst openings in Utah. Salt Lake City anchors the market as the state's primary business and healthcare hub, while Provo and surrounding Utah County draw heavily from the medical device corridor that runs south along the Wasatch Front, home to several device and diagnostics manufacturers.
Are there remote regulatory affairs analyst jobs in Utah?
Yes, and more than most fields, because regulatory affairs work is fundamentally documentation and review-based rather than hands-on. About 50% of regulatory affairs analyst openings tied to Utah are remote or hybrid as of September 2026, reflecting broad industry acceptance of distributed regulatory teams. Submission writing, labeling review, and compliance analysis are the functions most commonly offered on a remote or hybrid basis.
How can I get hired as a regulatory affairs analyst in Utah with little or no experience?
The most realistic entry path is moving laterally from a quality assurance, manufacturing, or clinical coordination role at a Utah life sciences company, where exposure to FDA-regulated processes transfers directly. Employers such as Merit Medical Systems and biotech firms along the Provo corridor regularly post associate regulatory affairs roles that accept candidates with quality or compliance backgrounds. Completing the RAC exam or an accredited regulatory affairs certificate program gives candidates a measurable credential edge over others at the entry level.
Where can I find and apply to regulatory affairs analyst jobs in Utah?
You can find and apply to regulatory affairs analyst jobs in Utah on Migrate Mate, which lists current openings across Salt Lake City, Provo, Ogden, and the broader Wasatch Front. Find roles that fit your background and apply directly to the employers posting them.
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