Save Job Back to Search Job Description Summary Similar JobsCompetitive compensation and benefits packageProfessional growth trajectory within the businessAbout Our ClientOur client is a leading industry partner that supplies medical device solutions to numerous major OEMs. They specialize in precision metal-fabricated components, along with select silicone handle applications for surgical devices.Job DescriptionPlan, coordinate, and execute quality control programs ensuring compliance to ISO13485 and FDA standardsInvestigate and address customer complaints - CAPAAssist with preparing and executing internal and external auditsHandle document and process controlsUpdate documentation and data within the QMSCreate and direct validations (IQ/OQ/PQ)Create PPAP documentationOther duties as assignedMPI 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 Applicant5+ years of quality experience in medical deviceUnderstanding of ISO13485 and FDA standardsExperience with metal fabrication required, CNC preferredGD&T/PPAP experienceKnowledge of QMS software and associated document controlCertifications a plusBachelors degree a plusSponsorship NOT offeredWhat's on OfferSalary ranging from 80,000-100,000+ depending on experience and interviews3 weeks of PTO- accrues from day oneFull medical benefit plans offered on day oneAncillary benefitsCompany paid holidaysRetirement plans offeredContactEd LieserQuote job refJN-012026-6913186Job summarySectorEngineering & ManufacturingSub SectorQuality, TechnicalIndustryIndustrial / ManufacturingLocationPleasant PrairieContract TypePermanentConsultant nameEd LieserJob ReferenceJN-012026-6913186
