{"schemaVersion":"jobsearcher.job.v1","id":"85236cacd8a794d18f518d23","url":"https://jobsearcher.com/jobs/85236cacd8a794d18f518d23","canonicalUrl":"https://jobsearcher.com/jobs/85236cacd8a794d18f518d23","title":"Quality Engineer","description":"Summary :\nWe are seeking a detail-oriented Quality Engineer with experience in the pharmaceutical industry to support quality engineering activities across manufacturing and laboratory operations. The ideal candidate will have hands‑on experience with deviations, CAPA, change control, validation, and GMP compliance.\n\nRoles & Responsibilities :\n\nSupport quality engineering activities for manufacturing and lab operations, including deviation investigations, CAPA, change control, and validation.\n\nReview batch records, SOPs, technical documents, and quality reports to ensure compliance with GMP, cGMP, and GLP standards.\n\nAssist in method development support, qualification activities, and validation documentation review for processes, equipment, and laboratory systems.\n\nCollaborate with QA, QC, Manufacturing, Validation, and Engineering teams to resolve quality issues and improve compliance.\n\nParticipate in root cause investigations for deviations, out‑of‑trend results, and process issues.\n\nSupport equipment qualification, calibration reviews, and maintenance documentation.\n\nReview and assess change control requests related to procedures, equipment, materials, and processes.\n\nMonitor quality metrics, trends, and recurring issues to drive continuous improvement.\n\nAssist in internal audits, compliance reviews, and inspection readiness.\n\nMaintain accurate and compliant quality documentation and records.\n\nEducation & Experience :\n\nBachelor's degree in Engineering, Life Sciences, Pharmacy, or related field.\n\n4+ years of experience in Quality Engineering within the pharmaceutical or life sciences industry.\n\nStrong knowledge of GMP, cGMP, GLP, and regulatory compliance requirements.\n\nExperience with deviation management, CAPA, change control, and validation processes.\n\nAbility to review and interpret technical documents, SOPs, and batch records.\n\nExperience supporting FDA audits or regulatory inspections.\n\nKnowledge of risk management and quality systems.\n\nFamiliarity with validation lifecycle (IQ, OQ, PQ).\n\n#J-18808-Ljbffr","company":"Creative Solutions Services","rawCompany":"creative solutions services","city":"Springfield","state":"IL","isRemote":false,"isActive":false,"createdAt":"2026-06-17T04:11:42.527Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325411","title":"Medicinal and Botanical Manufacturing","slug":"medicinal-and-botanical-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Quality Engineer","description":"Summary :\nWe are seeking a detail-oriented Quality Engineer with experience in the pharmaceutical industry to support quality engineering activities across manufacturing and laboratory operations. The ideal candidate will have hands‑on experience with deviations, CAPA, change control, validation, and GMP compliance.\n\nRoles & Responsibilities :\n\nSupport quality engineering activities for manufacturing and lab operations, including deviation investigations, CAPA, change control, and validation.\n\nReview batch records, SOPs, technical documents, and quality reports to ensure compliance with GMP, cGMP, and GLP standards.\n\nAssist in method development support, qualification activities, and validation documentation review for processes, equipment, and laboratory systems.\n\nCollaborate with QA, QC, Manufacturing, Validation, and Engineering teams to resolve quality issues and improve compliance.\n\nParticipate in root cause investigations for deviations, out‑of‑trend results, and process issues.\n\nSupport equipment qualification, calibration reviews, and maintenance documentation.\n\nReview and assess change control requests related to procedures, equipment, materials, and processes.\n\nMonitor quality metrics, trends, and recurring issues to drive continuous improvement.\n\nAssist in internal audits, compliance reviews, and inspection readiness.\n\nMaintain accurate and compliant quality documentation and records.\n\nEducation & Experience :\n\nBachelor's degree in Engineering, Life Sciences, Pharmacy, or related field.\n\n4+ years of experience in Quality Engineering within the pharmaceutical or life sciences industry.\n\nStrong knowledge of GMP, cGMP, GLP, and regulatory compliance requirements.\n\nExperience with deviation management, CAPA, change control, and validation processes.\n\nAbility to review and interpret technical documents, SOPs, and batch records.\n\nExperience supporting FDA audits or regulatory inspections.\n\nKnowledge of risk management and quality systems.\n\nFamiliarity with validation lifecycle (IQ, OQ, PQ).\n\n#J-18808-Ljbffr","datePosted":"2026-06-17T04:11:42.527Z","dateModified":"2026-06-17T04:11:42.527Z","hiringOrganization":{"@type":"Organization","name":"Creative Solutions Services","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Springfield","addressRegion":"IL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"85236cacd8a794d18f518d23"},"url":"https://jobsearcher.com/jobs/85236cacd8a794d18f518d23"}}