Save Job Back to Search Job Description Summary Similar JobsWork on a High Impact Team within a leading Medical ManufacturerHigh visibility position to site leadership; grow your career!About Our ClientThis organization is a global manufacturer specializing in the design, development, and production of complex medical devices and components. It offers fully integrated, end‑to‑end capabilities-from engineering and prototyping to full‑scale manufacturing, assembly, packaging, and sterilization-serving a wide range of clinical applications. With thousands of employees across more than 20 international locations, it provides the scale, cleanroom capacity, and technical depth needed to support highly regulated, life‑saving medical technologies. The company focuses exclusively on med‑tech, combining advanced engineering expertise with robust quality systems to help bring innovative devices to market efficiently and reliably.Job DescriptionIn this role, the Quality Engineer III will:Develop and implement quality control processes to meet regulatory and customer requirements.Analyze performance data to identify areas for improvement in engineering and manufacturing processes.Collaborate with cross-functional teams to resolve quality issues and implement corrective actions.Ensure compliance with industry standards and regulations in all quality-related activities.Conduct audits and inspections to monitor and maintain quality standards.Train and mentor team members on quality assurance best practices and procedures.Prepare detailed quality reports and present findings to management and stakeholders.Drive continuous improvement initiatives to enhance product quality and operational efficiency.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 Quality Engineer III will have:BS Degree in related discipline or High School Diploma with 10+years of relevant experience.5-8 years of relevant experience, preferably in the medical device industry.Ability to work cross-functionally and as a part of a project team.Experience in ISO 13485 industry.Ability to conduct root cause investigations using techniques such as FMEA, Fishbone, 5 Why, and 8D.Required experience with process validation (IQ, OQ, PQ, TMV).Proficiency in statistical tools (e.g., Gage R&R, Capability Analysis, ANOVA); Minitab experience is a plus.Proficiency in analyzing performance data and implementing improvement strategies.Excellent problem-solving skills and attention to detail.Effective communication and collaboration skills to work with cross-functional teams.Proven ability to lead quality improvement initiatives and mentor team members.What's on OfferOn offer for a Strong Quality Engineer III is:Competitive salary range of $90,000 to $105,000 annually.Opportunities for professional growth and development.Comprehensive medical, dental, and vision benefits.Company-paid life insurance and disability benefits.Generous paid time off (vacation, Sick leave, holidays).401k plan with company match.Supportive and collaborative work environment.Tuition reimbursementVoluntary benefits including life insurance long-term care, and legal coverage.ContactHarrison RocheQuote job refJN-012026-6933645Job summarySectorEngineering & ManufacturingSub SectorQuality, TechnicalIndustryIndustrial / ManufacturingLocationEnfieldContract TypePermanentConsultant nameHarrison RocheJob ReferenceJN-012026-6933645
