Quality Engineer

Company Description NovintiX is a leader in engineering services, dedicated to innovating and transforming industries like Medical Devices, Aerospace, Automotive, Consumer Electronics, and Industrial Equipment. With cutting-edge expertise in areas such as Product Engineering, Digital Solutions, Supply Chain Management, and Quality Compliance, we empower meaningful solutions that drive growth and excellence. Guided by a forward-thinking vision, NovintiX fosters innovation while prioritizing the success of both clients and employees. Our mission to provide best-in-class services underscores a commitment to shaping a sustainable, technology-driven future. Job Title: Quality Engineer - Medical Devices (Warsaw, IN)**Location: Warsaw, IndianaWork Arrangement: Full-time onsite (5 days/week)Key Responsibilities:Conduct receiving inspection using CMM measurement systems and standard metrology tools (vernier calipers, micrometers, gauges)Perform MRB (Material Review Board) reviews and disposition non-conforming materialsInterpret engineering drawings, blueprints, specifications, gage studies, and work instructionsExecute incoming material identification and quality verification processesSupport warehouse operations and inventory management system transactionsCollaborate with Quality Engineering team on process improvements and complianceRequired Qualifications:Bachelor’s degree in mechanical engineering (or equivalent)Minimum 8 years’ experience in medical device manufacturing/quality engineeringHands-on expertise with Windchill PLM and ETQ PLM systemsProven receiving inspection methodology experience in regulated medical device environmentCMM (Coordinate Measuring Machine) hands-on operation proficiencyMRB review and non-conformance disposition experience requiredTechnical Skills (Must-Have):CMM operation, vernier caliper, micrometer, gaugesWindchill, ETQ PLM systems - hands-on daily usageReceiving inspection and Gage R&R studiesRead/interpret engineering drawings, blueprints, specificationsInventory systems and material identification awarenessPreferred Qualifications:Experience with medical device quality standards (ISO 13485, FDA 21 CFR Part 820)Familiarity with statistical process control and capability analysisSix Sigma or Lean certification