Quality Assurance and Regulatory Affairs Manager

Professional DevelopmentEducation ReimbursementAbout Our ClientOur client is a premier contract manufacturer specializing in dietary supplements and nutritional products. With a state-of-the-art, cGMP-certified facility and an in-house R&D team, the company partners with leading and emerging brands to deliver innovative formulations, scalable production, and turnkey solutions. Known for its commitment to quality, compliance, and sustainable growth, this organization offers a collaborative environment where employees play a critical role in ensuring product integrity and regulatory excellence.Job DescriptionEnsure compliance with FDA (21 CFR 111), DSHEA, FTC, and global supplement regulations.Review/approve labels, claims, and marketing for regulatory accuracy.Maintain product dossiers, master files, and ingredient safety documentation.Manage agency submissions, audits, and client certifications (e.g., NSF, Organic, Kosher)Provide regulatory guidance during product development and commercializationMonitor evolving regulations and communicate impacts to stakeholdersOversee QMS aligned with cGMP, HACCP, ISO, and sanitation standardsLead internal, client, and regulatory audits, driving corrective actionsInvestigate quality incidents, CAPAs, deviations, and complaintsDevelop SOPs, batch records, and product specificationsManage supplier qualifications, lab performance, and raw material oversightTrain staff on GMP compliance, QA systems, and best practicesTrack KPIs, analyze trends, and implement process improvements 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 ApplicantBachelor's degree in Life Sciences, Chemistry, Nutrition, Food Science, or related field (Master's preferred)5+ years in QA/Regulatory compliance management within dietary supplement/food manufacturingStrong knowledge of FDA 21 CFR Part 111, DSHEA, FTC, USDA, HACCP, GMP, and ISO standardsHands-on experience with audits, documentation control, and CAPA managementExcellent organizational, communication, and leadership skillsWhat's on OfferBonus eligibilityMedical, dental, vision, and life insurance coverage401(k) with company matchPaid time off and holidaysEducation reimbursement and professional development opportunitiesContactEvalee TorresQuote job refJN-082025-6824016