{"schemaVersion":"jobsearcher.job.v1","id":"3f6ebf91ef327bd9021e48ae","url":"https://jobsearcher.com/jobs/3f6ebf91ef327bd9021e48ae","canonicalUrl":"https://jobsearcher.com/jobs/3f6ebf91ef327bd9021e48ae","title":"Validation Engineer","description":"Job Summary\nWe are seeking a highly motivated Validation Engineer to join our dynamic manufacturing and quality assurance team. In this role, you will be responsible for developing, executing, and overseeing validation protocols to ensure that manufacturing processes, equipment, and systems comply with industry standards and regulatory requirements. The ideal candidate will play a pivotal role in maintaining the integrity of quality systems, supporting compliance with ISO 13485, FDA regulations, HACCP, CGMP, ISO 9001, and other relevant standards. This position offers an opportunity to contribute to the continuous improvement of product quality and operational excellence through meticulous validation practices.\nResponsibilities\nDevelop comprehensive validation protocols for manufacturing processes, equipment qualification, and system validation in accordance with regulatory standards.\nExecute validation activities including installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ).\nCollaborate with cross-functional teams to ensure validation activities align with project timelines and quality objectives.\nConduct thorough documentation of validation results, deviations, and corrective actions to ensure traceability and compliance.\nPerform risk assessments related to manufacturing processes and implement mitigation strategies as needed.\nSupport ongoing calibration, maintenance, and revalidation efforts to sustain validated states.\nParticipate in quality audits and inspections related to validation activities to verify adherence to applicable standards.\nMaintain up-to-date knowledge of industry regulations such as ISO 13485, FDA guidelines, HACCP, CGMP, and ISO 9001.\nContribute to continuous improvement initiatives by analyzing validation data and recommending process enhancements.\nAssist in training team members on validation procedures and compliance requirements.\nExperience\nBachelor's degree in Engineering, Life Sciences, or a related field; advanced certifications in Validation or Quality Assurance are preferred.\nProven experience in validation within regulated manufacturing environments such as medical devices, pharmaceuticals, or food industries.\nStrong understanding of regulatory frameworks including ISO 13485, FDA regulations (21 CFR Part 11), HACCP principles, CGMP practices, and ISO 9001 standards.\nDemonstrated expertise in developing and executing validation protocols for equipment and processes.\nKnowledge of quality systems management including QA/QC procedures and quality audits.\nExcellent analysis skills with the ability to interpret data accurately and identify root causes of issues.\nProject management skills with the ability to prioritize tasks effectively while managing multiple projects simultaneously. This position offers an engaging environment where your expertise will directly impact product safety and quality. We welcome candidates committed to excellence in validation practices who are eager to contribute to our mission of delivering high-quality products through rigorous quality management systems.\nPay: $72,000.00 - $90,000.00 per year\nWork Location: In person","company":"Working World","rawCompany":"working world","city":"South Elgin","state":"IL","isRemote":false,"isActive":false,"createdAt":"2026-08-03T13:32:11.317Z","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":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"Job Summary\nWe are seeking a highly motivated Validation Engineer to join our dynamic manufacturing and quality assurance team. In this role, you will be responsible for developing, executing, and overseeing validation protocols to ensure that manufacturing processes, equipment, and systems comply with industry standards and regulatory requirements. The ideal candidate will play a pivotal role in maintaining the integrity of quality systems, supporting compliance with ISO 13485, FDA regulations, HACCP, CGMP, ISO 9001, and other relevant standards. This position offers an opportunity to contribute to the continuous improvement of product quality and operational excellence through meticulous validation practices.\nResponsibilities\nDevelop comprehensive validation protocols for manufacturing processes, equipment qualification, and system validation in accordance with regulatory standards.\nExecute validation activities including installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ).\nCollaborate with cross-functional teams to ensure validation activities align with project timelines and quality objectives.\nConduct thorough documentation of validation results, deviations, and corrective actions to ensure traceability and compliance.\nPerform risk assessments related to manufacturing processes and implement mitigation strategies as needed.\nSupport ongoing calibration, maintenance, and revalidation efforts to sustain validated states.\nParticipate in quality audits and inspections related to validation activities to verify adherence to applicable standards.\nMaintain up-to-date knowledge of industry regulations such as ISO 13485, FDA guidelines, HACCP, CGMP, and ISO 9001.\nContribute to continuous improvement initiatives by analyzing validation data and recommending process enhancements.\nAssist in training team members on validation procedures and compliance requirements.\nExperience\nBachelor's degree in Engineering, Life Sciences, or a related field; advanced certifications in Validation or Quality Assurance are preferred.\nProven experience in validation within regulated manufacturing environments such as medical devices, pharmaceuticals, or food industries.\nStrong understanding of regulatory frameworks including ISO 13485, FDA regulations (21 CFR Part 11), HACCP principles, CGMP practices, and ISO 9001 standards.\nDemonstrated expertise in developing and executing validation protocols for equipment and processes.\nKnowledge of quality systems management including QA/QC procedures and quality audits.\nExcellent analysis skills with the ability to interpret data accurately and identify root causes of issues.\nProject management skills with the ability to prioritize tasks effectively while managing multiple projects simultaneously. This position offers an engaging environment where your expertise will directly impact product safety and quality. We welcome candidates committed to excellence in validation practices who are eager to contribute to our mission of delivering high-quality products through rigorous quality management systems.\nPay: $72,000.00 - $90,000.00 per year\nWork Location: In person","datePosted":"2026-08-03T13:32:11.317Z","dateModified":"2026-08-03T13:32:11.317Z","hiringOrganization":{"@type":"Organization","name":"Working World","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"South Elgin","addressRegion":"IL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"3f6ebf91ef327bd9021e48ae"},"url":"https://jobsearcher.com/jobs/3f6ebf91ef327bd9021e48ae"}}