Save Job Back to Search Job Description Summary Similar JobsOwn quality on complex medical products from design through scale-upSenior-level influence in a fast-growing, high-tech manufacturing siteAbout Our ClientThis organization is a rapidly growing, technology-driven manufacturer supporting highly regulated products used in critical applications. They combine advanced engineering capabilities with full-scale production, offering a fast-paced environment where quality has real visibility and impact.Job DescriptionLead quality engineering activities supporting production and manufacturing engineeringEnsure compliance with ISO 13485 and applicable FDA regulations across projectsDrive CAPA, nonconformance management, change control, and audit readinessAuthor and execute validation, qualification, and risk management documentationSupport supplier quality activities, including audits and performance monitoringMentor junior engineers and contribute to continuous improvement initiativesMPI 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 Senior Quality Engineer should have:Bachelor's degree in Engineering or related technical discipline5+ years of experience in a Quality Engineering roleExperience in regulated manufacturing (medical device strongly preferred)Working knowledge of ISO 13485 and 21 CFR 820Background in CAPA, audits, validation, and process controlStrong communication skills with a proactive, hands-on mindsetWhat's on OfferCompetitive salary ranging from $100,000 to $120,000 USD.Senior role with ownership across high-value, complex projectsMix of hands-on floor work and system-level quality leadershipStrong, collaborative culture with visible leadership supportExposure to diverse products and customers in regulated industriesCompetitive compensation, profit sharing, and strong benefitsIf you are passionate about quality assurance and seeking a permanent role as a Senior Quality Engineer, we encourage you to apply.ContactCian TroyQuote job refJN-022026-6958134Job summarySectorEngineering & ManufacturingSub SectorQuality, TechnicalIndustryIndustrial / ManufacturingLocationHudsonContract TypePermanentConsultant nameCian TroyJob ReferenceJN-022026-6958134
