Save Job Back to Search Job Description Summary Similar JobsCross-functional exposure in a growing brand environmentHigh-impact ownershipAbout Our ClientThe hiring organization is a fast growing company within the cosmetic and personal care industry. With a strong reputation for delivering top-tier products, they are dedicated to maintaining quality and compliance across their operations.Job DescriptionManage formula approval documentation and coordinate communication with contract manufacturers, including test plans and regulatory requirementsOversee product testing processes, including sample coordination, protocols, vendor quotes, and method validation to ensure accuracy, reliability, and regulatory compliance of testing proceduresCollaborate with regulatory partners to collect and maintain formula, raw material, and compliance documentationEnsure accuracy and compliance of product labeling, artwork, and master documentationSupport global product registrations (U.S. and international markets, as applicable)Maintain comprehensive product dossiers / PIF documentation for all SKUsReview and interpret testing results, ensuring validated methods are used and timelines and compliance standards are metIdentify and resolve stability or compatibility issues in partnership with manufacturersCommunicate testing status, risks, and timelines to cross-functional stakeholdersSupport pilot runs, production batches, and line trials, including on-site visits as neededReview batch records, finished goods, and Certificates of Analysis (COAs)Maintain organized digital records of quality and production documentationManage change control processes across product lifecycle updates, including assessment of impact to validated methodsSupport formula and packaging revisions to maintain complianceParticipate in audits, vendor qualification, and GMP compliance initiatives, including evaluation of validated testing methods at partner facilitiesMonitor regulatory trends and provide guidance to internal teamsDrive resolution of quality issues and CAPAs (Corrective and Preventive Actions)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.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 Director of QA & Regulatory should have:4-5+ years of experience in Quality Assurance within cosmetics or personal care, OTC experienceExperience supporting or partnering with Regulatory Affairs functionsExperience with product safety, stability, and clinical testing, including familiarity with method validation principlesStrong understanding of global regulatory frameworks (FDA, EU, etc.)Exceptional documentation, organization, and attention to detailWhat's on OfferCompetitive annual salary ranging from $120,000 to $145,000.Unlimited PTO to support work-life balance.Opportunity to work with a reputable company in the OTC personal care industry.Collaborative and supportive team environment.If you're ready to take the next step in your career as a Sr Manager of QA & Regulatory, apply today to join this exciting opportunity in West HollywoodContactBrinn BorowskyQuote job refJN-032026-6979604Job summarySectorEngineering & ManufacturingSub SectorQuality, TechnicalIndustryFMCG (Fast Moving Consumer Goods)LocationWest HollywoodContract TypePermanentConsultant nameBrinn BorowskyJob ReferenceJN-032026-6979604