{"schemaVersion":"jobsearcher.job.v1","id":"91251678bb0982df91637f37","url":"https://jobsearcher.com/jobs/91251678bb0982df91637f37","canonicalUrl":"https://jobsearcher.com/jobs/91251678bb0982df91637f37","title":"Validation Engineer","description":"A company is looking for a Validation Engineer to support validation activities in a CDMO environment.\r\nKey Responsibilities\r\nGenerate and execute validation lifecycle documentation for GMP regulated assets\r\nSupport validation activities for tech transfer projects, including authoring and executing validation documents\r\nWrite, review, and revise qualification and verification documents and prepare summary reports for validation activities\r\nQualifications and Requirements\r\nBachelor's degree in a life science, engineering, or related technical field\r\n4-7 years of experience in the biotech, pharmaceutical, or medical device industry\r\nStrong knowledge of FDA cGMP requirements and risk-based validation principles\r\nHands-on validation experience in equipment and computerized systems\r\nExperience generating protocols for automated production systems and writing IQ, OQ, PQ, and CSV reports","company":"Virtual Vocations","rawCompany":"virtual vocations","city":"Carson","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-04-14T03:23:13.221Z","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":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"A company is looking for a Validation Engineer to support validation activities in a CDMO environment.\r\nKey Responsibilities\r\nGenerate and execute validation lifecycle documentation for GMP regulated assets\r\nSupport validation activities for tech transfer projects, including authoring and executing validation documents\r\nWrite, review, and revise qualification and verification documents and prepare summary reports for validation activities\r\nQualifications and Requirements\r\nBachelor's degree in a life science, engineering, or related technical field\r\n4-7 years of experience in the biotech, pharmaceutical, or medical device industry\r\nStrong knowledge of FDA cGMP requirements and risk-based validation principles\r\nHands-on validation experience in equipment and computerized systems\r\nExperience generating protocols for automated production systems and writing IQ, OQ, PQ, and CSV reports","datePosted":"2026-04-14T03:23:13.221Z","dateModified":"2026-04-14T03:23:13.221Z","hiringOrganization":{"@type":"Organization","name":"Virtual Vocations","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Carson","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"91251678bb0982df91637f37"},"url":"https://jobsearcher.com/jobs/91251678bb0982df91637f37"}}