Save Job Back to Search Job Description Summary Similar JobsCareer Growth & Stability - Join a rapidly growing contract manufacturer!Healthcare coverage, 01(k) with company contribution, and paid time offAbout Our ClientMy client is a growing contract manufacturer specializing in high-precision components for the medical industry. They provide advanced manufacturing capabilities, including CNC grinding, Swiss turning, deep-hole drilling, and catheter processing. Their operations span multiple facilities, supporting a range of medical markets, including orthopedics, interventional therapies, and minimally invasive surgery. The company has expanded significantly in recent years and continues to invest in innovation and process excellence. They are based out of Franklin, MA.Job Description The Quality Engineer, Medical Device Manufacturing, will:Develop and implement quality policies, procedures, and compliance initiativesLead investigations into non-conformances, customer complaints, and CAPAsSupport manufacturing process validation and product qualification effortsManage change control and supplier/customer quality notificationsDefine and oversee inspection and testing requirements for productionAnalyze production data, customer feedback, and scrap rates to drive improvementsConduct internal audits to ensure ongoing ISO 13485 complianceCollaborate with cross-functional teams to enhance quality processesTrain and mentor staff on quality-related best practicesWork closely with customers and suppliers to resolve quality concernsSupport continuous improvement projects using Lean methodologiesOnsite at our Franklin, MA facilityMPI 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 ApplicantProven experience in quality control / quality engineering within a regulated manufacturing environment (medical device preferred)Strong analytical skills with the ability to investigate and resolve quality issuesHands-on experience managing CAPAs and driving corrective actionsCustomer-facing experience, with strong communication and problem-solving abilitiesWorking knowledge of ISO 13485 and quality system complianceAbility to define and implement in-process and incoming inspection requirementsExperience with risk analysis techniques, including PFMEAProficiency in blueprint reading, including GD&TFamiliarity with measurement tools such as optical comparators and micrometersProject management skills with the ability to manage multiple initiativesExperience with quality software tools, including Microsoft Office and ERP/MES systemsPositive attitude and ability to work in a fast-paced, collaborative environmentLocal to Franklin, MAWhat's on OfferComprehensive benefits package, including healthcare, retirement plans, and paid time offCareer growth within a fast-growing, quality-driven organizationOpportunity to work with cutting-edge manufacturing technologiesCollaborative team environment with strong leadership supportContactIsabel ReynesQuote job refJN-022025-6674257Job summarySectorEngineering & ManufacturingSub SectorQuality, TechnicalIndustryIndustrial / ManufacturingLocationFranklinContract TypePermanentConsultant nameIsabel ReynesJob ReferenceJN-022025-6674257