Save Job Back to Search Job Description Summary Similar JobsJoin a cutting-edge medical technology environmentLead quality engineering activities across product development and validation.About Our ClientThis organization is a rapidly expanding medical‑technology innovator focused on developing life‑changing therapeutic solutions. Its teams are united by a shared purpose and a passion for engineering excellence. The culture encourages creativity, cross‑functional collaboration, and continuous learning. Employees thrive in a supportive, mission‑oriented environment designed to empower bold ideas. The company is committed to growth, inclusivity, and delivering meaningful impact to patients worldwide.Job DescriptionLead quality engineering activities across product development, validation, and manufacturingPartner with R&D, manufacturing, and regulatory teams to ensure compliance with FDA and ISO standardsOversee risk management processes, including FMEA and hazard analysisDrive root cause investigations, CAPA activities, and nonconformance resolutionSupport internal and external audits and regulatory inspectionsDevelop and improve quality systems, procedures, and documentationAnalyze quality data to identify trends and implement corrective actionsMentor junior engineers and influence best practices across the organizationMPI 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 Engineering or a related technical disciplineExtensive experience in quality engineering within the medical device or regulated industryStrong knowledge of FDA regulations, ISO 13485, and quality system requirementsProven experience with CAPA, nonconformances, and risk management toolsFamiliarity with validation processes, including IQ/OQ/PQExcellent problem-solving, analytical, and communication skillsAbility to work cross-functionally in a fast-paced environmentASQ certification (CQE or similar) preferredWhat's on OfferCompetitive base salary aligned with experience.Comprehensive medical benefits with full employee and family coverage.Paid vacation, holidays, floating days, and sick time.401(k) program with employer match.Annual performance bonus eligibility.A collaborative, inclusive culture that encourages innovation and personal growth.ContactConnor ColomboQuote job refJN-062026-7037695Job summarySectorLife SciencesSub SectorMedical devicesIndustryIndustrial / ManufacturingLocationCherry HillContract TypePermanentConsultant nameConnor ColomboJob ReferenceJN-062026-7037695
