{"schemaVersion":"jobsearcher.job.v1","id":"1a0fbda15cd5fe7e7b8ffae5","url":"https://jobsearcher.com/jobs/1a0fbda15cd5fe7e7b8ffae5","canonicalUrl":"https://jobsearcher.com/jobs/1a0fbda15cd5fe7e7b8ffae5","title":"Sr. Design Quality Engineering","description":"Sr. Design Quality Engineering\r\nLocation: Irvine, California\r\nJob Type: C2C | Hybrid\r\nPay Rate: $50/hr\r\nIndustry: Manufacturing / Medical Devices\r\nEnd Date: 01-Jan-2026\r\nJob Description We are seeking a Sr. Design Quality Engineering professional experienced in ensuring product quality compliance, supporting risk management activities, and leading verification and validation processes. The role requires strong collaboration with cross-functional teams, hands-on involvement in design control, and the ability to resolve quality issues through structured problem-solving and risk-based approaches.\r\nResponsibilities Ensure quality engineering activities meet regulatory and internal standards.\r\nCreate and maintain product risk management documentation (Risk Plans, DFMEA, Risk Assessments, Risk Reports).\r\nSupport development and execution of V&V plans, protocols, and reports.\r\nPerform Test Method Validation and process validation (PFMEA, IQ, OQ, PQ).\r\nUse statistical tools such as Minitab for data analysis.\r\nOversee product testing to ensure compliance with applicable requirements.\r\nApply Design Control principles to support sustaining engineering and product updates.\r\nResolve quality issues and support design changes with cross-functional teams.\r\nApply risk management techniques to identify and mitigate product risks.\r\nUse structured problem-solving methodologies to address product and process challenges.\r\nPrepare technical documentation, reports, and presentations for stakeholders.\r\nRequired Qualifications Experience with quality engineering in manufacturing or medical device environments.\r\nStrong knowledge of design control, risk management, and process validation.\r\nHands-on experience with DFMEA, PFMEA, V&V activities, and statistical tools (Minitab).\r\nAbility to support sustaining engineering and design updates.\r\nStrong analytical, communication, and problem-solving skills.\r\nExperience collaborating with engineering, manufacturing, and quality teams.\r\nJ-18808-Ljbffr","company":"Simarn Solutions","rawCompany":"simarn solutions","city":"Irvine","state":"KY","isRemote":false,"isActive":false,"createdAt":"2026-04-09T09:04:12.262Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"}],"industries":[{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Sr. Design Quality Engineering","description":"Sr. Design Quality Engineering\r\nLocation: Irvine, California\r\nJob Type: C2C | Hybrid\r\nPay Rate: $50/hr\r\nIndustry: Manufacturing / Medical Devices\r\nEnd Date: 01-Jan-2026\r\nJob Description We are seeking a Sr. Design Quality Engineering professional experienced in ensuring product quality compliance, supporting risk management activities, and leading verification and validation processes. The role requires strong collaboration with cross-functional teams, hands-on involvement in design control, and the ability to resolve quality issues through structured problem-solving and risk-based approaches.\r\nResponsibilities Ensure quality engineering activities meet regulatory and internal standards.\r\nCreate and maintain product risk management documentation (Risk Plans, DFMEA, Risk Assessments, Risk Reports).\r\nSupport development and execution of V&V plans, protocols, and reports.\r\nPerform Test Method Validation and process validation (PFMEA, IQ, OQ, PQ).\r\nUse statistical tools such as Minitab for data analysis.\r\nOversee product testing to ensure compliance with applicable requirements.\r\nApply Design Control principles to support sustaining engineering and product updates.\r\nResolve quality issues and support design changes with cross-functional teams.\r\nApply risk management techniques to identify and mitigate product risks.\r\nUse structured problem-solving methodologies to address product and process challenges.\r\nPrepare technical documentation, reports, and presentations for stakeholders.\r\nRequired Qualifications Experience with quality engineering in manufacturing or medical device environments.\r\nStrong knowledge of design control, risk management, and process validation.\r\nHands-on experience with DFMEA, PFMEA, V&V activities, and statistical tools (Minitab).\r\nAbility to support sustaining engineering and design updates.\r\nStrong analytical, communication, and problem-solving skills.\r\nExperience collaborating with engineering, manufacturing, and quality teams.\r\nJ-18808-Ljbffr","datePosted":"2026-04-09T09:04:12.262Z","dateModified":"2026-04-09T09:04:12.262Z","hiringOrganization":{"@type":"Organization","name":"Simarn Solutions","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Irvine","addressRegion":"KY","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"1a0fbda15cd5fe7e7b8ffae5"},"url":"https://jobsearcher.com/jobs/1a0fbda15cd5fe7e7b8ffae5"}}