{"schemaVersion":"jobsearcher.job.v1","id":"998fa78f42e03e9ccd546e50","url":"https://jobsearcher.com/jobs/998fa78f42e03e9ccd546e50","canonicalUrl":"https://jobsearcher.com/jobs/998fa78f42e03e9ccd546e50","title":"Validation Engineer","description":"At Cadence, we improve product performance by building solution-oriented partnerships with our customers and delivering highly technical, measurable outcomes across medical, life sciences, automotive, and other advanced industries.\nWe’re an engineering company at heart—with over 75 engineers across our organization—and have built a legacy of over three decades of manufacturing excellence by doing what others consider impossible.\nPosition Overview:\nWe are seeking a highly motivated Validation Engineer onsite at Cranberry Twp., Sturgeon Bay, WI, Suffield, CT or Cranston, RI sites, to lead and support validation activities across multiple projects at our facility. This role is critical in ensuring compliance with regulatory standards (FDA, ISO 13485, 21 CFR Part 820), working closely with engineering, QA, and manufacturing teams.\nKey Responsibilities:\nDevelop and execute validation protocols. (IQ, OQ, PQ, TMV)\nMaintain detailed validation documentation. (VMPs, reports, SOPs)\nConduct risk assessments and manage change controls.\nEnsure regulatory compliance. (GMP, GLP, CSV, data integrity)\nCollaborate cross-functionally to support validation strategy and training.\nMonitor system performance and lead requalification activities.\nQualify suppliers and vendors.\nContribute to process improvements and continuous improvement initiatives.\nQualifications:\nBachelor’s in Engineering, Life Sciences, or related field.\n3+ years' experience in validation or quality in a regulated industry.\nKnowledge of FDA, ISO 13485, 21 CFR Part 820 standards.\nProficiency in Microsoft Suite; experience with validation software.\nStrong communication, documentation, and analytical skills.\nPreferred: Lean/Six Sigma certification; experience with LMS systems.\nWork Environment:\nSplit between office and production floor. Requires clear communication, computer use, and occasional physical movement around facility.\nWe are not offering sponsorship at this time for this position.","company":"Cadence","rawCompany":"cadence","city":"Suffield","state":"CT","isRemote":false,"isActive":false,"createdAt":"2026-04-14T11:19:56.954Z","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":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"At Cadence, we improve product performance by building solution-oriented partnerships with our customers and delivering highly technical, measurable outcomes across medical, life sciences, automotive, and other advanced industries.\nWe’re an engineering company at heart—with over 75 engineers across our organization—and have built a legacy of over three decades of manufacturing excellence by doing what others consider impossible.\nPosition Overview:\nWe are seeking a highly motivated Validation Engineer onsite at Cranberry Twp., Sturgeon Bay, WI, Suffield, CT or Cranston, RI sites, to lead and support validation activities across multiple projects at our facility. This role is critical in ensuring compliance with regulatory standards (FDA, ISO 13485, 21 CFR Part 820), working closely with engineering, QA, and manufacturing teams.\nKey Responsibilities:\nDevelop and execute validation protocols. (IQ, OQ, PQ, TMV)\nMaintain detailed validation documentation. (VMPs, reports, SOPs)\nConduct risk assessments and manage change controls.\nEnsure regulatory compliance. (GMP, GLP, CSV, data integrity)\nCollaborate cross-functionally to support validation strategy and training.\nMonitor system performance and lead requalification activities.\nQualify suppliers and vendors.\nContribute to process improvements and continuous improvement initiatives.\nQualifications:\nBachelor’s in Engineering, Life Sciences, or related field.\n3+ years' experience in validation or quality in a regulated industry.\nKnowledge of FDA, ISO 13485, 21 CFR Part 820 standards.\nProficiency in Microsoft Suite; experience with validation software.\nStrong communication, documentation, and analytical skills.\nPreferred: Lean/Six Sigma certification; experience with LMS systems.\nWork Environment:\nSplit between office and production floor. Requires clear communication, computer use, and occasional physical movement around facility.\nWe are not offering sponsorship at this time for this position.","datePosted":"2026-04-14T11:19:56.954Z","dateModified":"2026-04-14T11:19:56.954Z","hiringOrganization":{"@type":"Organization","name":"Cadence","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Suffield","addressRegion":"CT","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"998fa78f42e03e9ccd546e50"},"url":"https://jobsearcher.com/jobs/998fa78f42e03e9ccd546e50"}}