Save Job Back to Search Job Description Summary Similar JobsOpportunity to have an impact on people's livesBonus Eligible!About Our Client Our client is a well-established medical device manufacturer recognized for its innovative electro-mechanical products and technologies. As the company continues to expand and launch a new generation of products, they are seeking a professional who can contribute to product quality, regulatory compliance, and continuous improvement initiatives. Operating under ISO 13485-certified quality standards, the organization serves customers in nearly 50 countries and offers the opportunity to make a meaningful impact through products that enhance patient outcomes worldwide.Job DescriptionProduct Review & ReleaseReview Device History Records (DHRs), manufacturing documentation, inspection data, and quality records to confirm products meet release requirements.Perform final quality review and disposition of production lots in accordance with established procedures and regulatory standards.Verify completion of all required manufacturing, testing, inspection, and labeling activities before product release.Identify and escalate quality concerns, deviations, or nonconformances that could affect product acceptance or release decisions.Support investigations and corrective actions related to product release issues.Complaint Management & InvestigationReview, document, and process customer complaints in compliance with established quality and regulatory procedures.Assess complaints for completeness, risk level, investigation needs, and potential regulatory reporting requirements.Participate in complaint investigations to determine root cause and recommend corrective actions when necessary.Analyze complaint trends and performance data to identify recurring issues and emerging quality concerns.Escalate significant quality events and potentially reportable issues to Quality and Regulatory teams.Maintain accurate, complete, and compliant complaint documentation and records.Internal & Supplier AuditsConduct internal and supplier audits in accordance with approved audit schedules and procedures.Evaluate quality management system processes for compliance with ISO 13485, ISO 14971, FDA requirements, and internal standards.Document audit observations, findings, and opportunities for continuous improvement.Verify implementation and effectiveness of corrective actions resulting from audit findings.Support audit readiness initiatives, regulatory inspections, and ongoing compliance 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.The Successful ApplicantBachelor's Degree (Engineering-related preferred)2+ years of manufacturing experience within qualityUnderstanding of ISO 9001Experience with electro-mechanical processes is preferredMedical device experienceCombination device experience is preferredExperience working with capital equipmentExperience working with sterile products is preferredUnderstanding of ISO 14971 and UL 60601 is preferredCQE certification is preferredSix Sigma belt is preferredSponsorship is not providedWhat's on OfferBase salary between $60k-$80kHealth, dental, vision401(k) matching3 weeks PTO4% annual bonus incentiveContactGeorge SherlockQuote job refJN-092026-7101172Job summarySectorEngineering & ManufacturingSub SectorQuality, TechnicalIndustryIndustrial / ManufacturingWhereElk Grove VillageContract TypePermanentConsultant nameGeorge SherlockJob ReferenceJN-092026-7101172