Save Job Back to Search Job Description Summary Similar JobsGrowing ManufacturerGrowth OpportunityAbout Our ClientOur client is a well-established, mid-sized company operating in the supplements/OTC industry.Job DescriptionExperince working with Supplements or OTC is required.Experience with FDA regulatory frameworks, including 21 CFR Parts 111, 101, and 330, with the ability to interpret and apply regulations to OTC drug monographs and dietary supplement requirements.Strong Labeling Compliance expertise, including review of Supplement Facts / Drug Facts panels, ingredient statements, allergen labeling, claims language, and packaging artwork to ensure alignment with FDA, FTC, and cGMP requirements.Hands‑on experience conducting claims substantiation, reviewing scientific literature, and ensuring all structure/function and OTC‑permitted claims are properly supported and risk‑appropriate.Ability to review and assess raw materials, including COAs, SDSs, specifications, and vendor documentation for regulatory acceptability and compliance with internal quality standards.Familiarity with product development workflows, including evaluating ingredient permissibility, tracking formulation changes, advising on regulatory risks, and supporting cross‑functional teams (R&D, Quality, Marketing, Legal).Knowledge of international regulatory requirements (preferred but not required), including Canada NNHP, EU/UK supplement standards, and global OTC compliance frameworks.MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants. Michael Page will consider for employment qualified applicants with criminal histories in a manner consistent with the Los Angeles Fair Chance Initiative for Hiring Ordinance.MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.The Successful ApplicantA successful Regulatory Affairs Specialist should have:Knowledge of regulatory standards and requirements in the Engineering & Manufacturing sector.Strong organizational skills and attention to detail for managing documentation.Excellent communication abilities to liaise with internal teams and external regulatory bodies.Problem-solving skills to navigate complex regulatory challenges.Familiarity with compliance audits and inspections.What's on OfferCompetitive annual salary ranging from $60,000 to $80,000 USD.Comprehensive benefits package including 401(k).Opportunity to work in a thriving and innovative industry.Be part of a collaborative and supportive work environment.If you're ready to take the next step in your career as a Regulatory Affairs Specialist in Los Angeles, we encourage you to apply today!ContactRishab VaidhyanathanQuote job refJN-032026-6984592Job summarySectorEngineering & ManufacturingSub SectorQuality, TechnicalIndustryHealthcare / PharmaceuticalLocationCaliforniaContract TypePermanentConsultant nameRishab VaidhyanathanJob ReferenceJN-032026-6984592