{"schemaVersion":"jobsearcher.job.v1","id":"3be14ef92ef235c46887b768","url":"https://jobsearcher.com/jobs/3be14ef92ef235c46887b768","canonicalUrl":"https://jobsearcher.com/jobs/3be14ef92ef235c46887b768","title":"Quality Engineer","description":"Job Title: Quality Engineer\nLocation: Temecula, CA 92591\nDuration: 6 Months\nWork Arrangement: 100% Onsite\nPay Range: $40 - $43 per hour (W2)\n\nWe are seeking a “Quality Engineer” to join one of our leading healthcare clients.\n\nPosition Summary\nThe Quality Engineer, Regulatory Compliance will support quality system compliance activities to ensure adherence to applicable regulatory requirements, corporate quality standards, and internal procedures. The individual will partner with Quality, Manufacturing, Operations, and other cross-functional teams to drive compliance initiatives, support audits and inspections, manage quality records, and facilitate continuous improvement activities within the Quality Management System (QMS).\n\nKey Responsibilities\n\nSupport compliance with FDA Quality System Regulations, QMSR, ISO 13485, and applicable corporate quality requirements.\nConduct quality system assessments and compliance reviews to identify risks and improvement opportunities.\nSupport internal, external, and regulatory audits and inspections.\nReview and approve quality records, including deviations, nonconformances, change controls, and CAPAs.\nAnalyze quality and compliance metrics to identify trends and drive continuous improvement initiatives.\nCollaborate with cross-functional teams to ensure timely closure of quality system actions.\nSupport implementation and maintenance of Quality Management System processes and procedures.\nPrepare quality and compliance reports, audit responses, and management review inputs.\nAssist with inspection readiness activities and regulatory commitments.\nRequired Qualifications\nBachelor's degree in Engineering, Quality, Life Sciences, or related technical discipline.\n0-3 years of experience in Quality Engineering, Quality Systems, or Regulatory Compliance within a regulated industry.\nStrong analytical, problem-solving, and technical writing skills.\nExcellent communication and stakeholder management skills.\nPreferred Qualifications\nMedical device industry experience.\nCertified Quality Engineer (CQE), Certified Quality Auditor (CQA), or equivalent certification.\nExperience with electronic quality management systems (eQMS)\nWorking knowledge of FDA regulations, Quality Management Systems, and ISO 13485 requirements.\nExperience with CAPA, investigations, change management, nonconformance management, and risk assessment processes\nExperience supporting audits and regulatory inspections.\nSkills\nQuality Systems Compliance\nAudit Support\nRegulatory Compliance\nData Analysis and Trending\nRisk Assessment\nTechnical Documentation\nContinuous Improvement\n\nWe are looking for the candidate who are eligible to work with any employers without sponsorship.\n\nIf you’re interested, please click “Apply” button.","company":"Experis","rawCompany":"experis","city":"Temecula","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-09-02T11:13:02.579Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"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"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Quality Engineer","description":"Job Title: Quality Engineer\nLocation: Temecula, CA 92591\nDuration: 6 Months\nWork Arrangement: 100% Onsite\nPay Range: $40 - $43 per hour (W2)\n\nWe are seeking a “Quality Engineer” to join one of our leading healthcare clients.\n\nPosition Summary\nThe Quality Engineer, Regulatory Compliance will support quality system compliance activities to ensure adherence to applicable regulatory requirements, corporate quality standards, and internal procedures. The individual will partner with Quality, Manufacturing, Operations, and other cross-functional teams to drive compliance initiatives, support audits and inspections, manage quality records, and facilitate continuous improvement activities within the Quality Management System (QMS).\n\nKey Responsibilities\n\nSupport compliance with FDA Quality System Regulations, QMSR, ISO 13485, and applicable corporate quality requirements.\nConduct quality system assessments and compliance reviews to identify risks and improvement opportunities.\nSupport internal, external, and regulatory audits and inspections.\nReview and approve quality records, including deviations, nonconformances, change controls, and CAPAs.\nAnalyze quality and compliance metrics to identify trends and drive continuous improvement initiatives.\nCollaborate with cross-functional teams to ensure timely closure of quality system actions.\nSupport implementation and maintenance of Quality Management System processes and procedures.\nPrepare quality and compliance reports, audit responses, and management review inputs.\nAssist with inspection readiness activities and regulatory commitments.\nRequired Qualifications\nBachelor's degree in Engineering, Quality, Life Sciences, or related technical discipline.\n0-3 years of experience in Quality Engineering, Quality Systems, or Regulatory Compliance within a regulated industry.\nStrong analytical, problem-solving, and technical writing skills.\nExcellent communication and stakeholder management skills.\nPreferred Qualifications\nMedical device industry experience.\nCertified Quality Engineer (CQE), Certified Quality Auditor (CQA), or equivalent certification.\nExperience with electronic quality management systems (eQMS)\nWorking knowledge of FDA regulations, Quality Management Systems, and ISO 13485 requirements.\nExperience with CAPA, investigations, change management, nonconformance management, and risk assessment processes\nExperience supporting audits and regulatory inspections.\nSkills\nQuality Systems Compliance\nAudit Support\nRegulatory Compliance\nData Analysis and Trending\nRisk Assessment\nTechnical Documentation\nContinuous Improvement\n\nWe are looking for the candidate who are eligible to work with any employers without sponsorship.\n\nIf you’re interested, please click “Apply” button.","datePosted":"2026-09-02T11:13:02.579Z","dateModified":"2026-09-02T11:13:02.579Z","hiringOrganization":{"@type":"Organization","name":"Experis","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Temecula","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"3be14ef92ef235c46887b768"},"url":"https://jobsearcher.com/jobs/3be14ef92ef235c46887b768"}}