Save Job Back to Search Job Description Summary Similar JobsJoin a global medical device leader improving patient outcomesHigh-growth site with exposure to machining, quality & operationsAbout Our ClientOur client is a global manufacturing organization that partners with leading innovators to develop and produce highly engineered products used around the world. With significant investment in technology, advanced manufacturing capabilities, and continuous improvement, the company offers strong career growth and exposure to complex, highly regulated production environments.Job DescriptionSupport manufacturing operations to ensure compliance with quality systems and regulatory requirements.Lead quality investigations, CAPAs, non-conformance activities, and root cause analysis efforts.Drive process improvements, risk analysis, validations, and continuous improvement initiatives.Partner with Manufacturing Engineering on process validations, capability studies, and product launches.Develop and maintain inspection methods, control plans, and quality documentation.Support audits, regulatory inspections, complaint investigations, and supplier quality activities.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 Quality Engineer should have:Bachelor's degree in Engineering or a related technical discipline preferred.2-5 years of Quality Engineering experience within medical device or regulated manufacturing environments.Experience with CAPA, root cause analysis, risk management, and quality systems.Knowledge of FDA, ISO 13485, MDSAP, ISO 14971, or similar regulatory standards.Strong analytical skills with experience utilizing statistical quality tools and methodologies.Excellent communication skills and ability to collaborate across operations, engineering, suppliers, and customers.What's on OfferCompetitive salary ranging from $75,000 to $95,000 annually.Join a global organizationWork within the medical device industry manufacturing products that improve livesGain exposure to advanced CNC machining, Swiss machining, and precision manufacturing environmentsStrong interaction with Quality, Manufacturing, Operations, and Leadership teamsInterested? Apply today.ContactCian TroyQuote job refJN-092026-7105496Job summarySectorEngineering & ManufacturingSub SectorQuality, TechnicalIndustryIndustrial / ManufacturingWhereSturbridgeContract TypePermanentConsultant nameCian TroyJob ReferenceJN-092026-7105496
