{"schemaVersion":"jobsearcher.job.v1","id":"d5026c2f66fabeb3649857c8","url":"https://jobsearcher.com/jobs/d5026c2f66fabeb3649857c8","canonicalUrl":"https://jobsearcher.com/jobs/d5026c2f66fabeb3649857c8","title":"Validation Specialist","description":"Roles & Responsibilities Support cleaning validation activities, protocol execution, sampling, and documentation. Perform temperature mapping and requalification of controlled temperature units. Execute IQ/OQ/PQ, requalification, and periodic review for GMP equipment and utilities. Support commissioning, installation, and qualification of new or modified equipment. Assist with equipment troubleshooting alongside Engineering and Operations. Generate validation documentation following cGMP, GDP, and SOP requirements. Support validation lifecycle activities, change controls, investigations, and CAPAs. Participate in audit readiness and regulatory inspection support. Bachelor's degree in Engineering, Life Sciences, or related discipline required. 5+ years of hands-on validation experience with GMP equipment and utilities.","company":"Katalyst CRO","rawCompany":"katalyst cro","city":"Denver","state":"CO","isRemote":false,"isActive":false,"createdAt":"2026-07-11T12:41:23.111Z","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":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"334513","title":"Instruments and Related Products Manufacturing for Measuring, Displaying, and Controlling Industrial Process Variables","slug":"instruments-and-related-products-manufacturing-for-measuring-displaying-and-controlling-industrial-process-variables"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Specialist","description":"Roles & Responsibilities Support cleaning validation activities, protocol execution, sampling, and documentation. Perform temperature mapping and requalification of controlled temperature units. Execute IQ/OQ/PQ, requalification, and periodic review for GMP equipment and utilities. Support commissioning, installation, and qualification of new or modified equipment. Assist with equipment troubleshooting alongside Engineering and Operations. Generate validation documentation following cGMP, GDP, and SOP requirements. Support validation lifecycle activities, change controls, investigations, and CAPAs. Participate in audit readiness and regulatory inspection support. Bachelor's degree in Engineering, Life Sciences, or related discipline required. 5+ years of hands-on validation experience with GMP equipment and utilities.","datePosted":"2026-07-11T12:41:23.111Z","dateModified":"2026-07-11T12:41:23.111Z","hiringOrganization":{"@type":"Organization","name":"Katalyst CRO","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Denver","addressRegion":"CO","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"d5026c2f66fabeb3649857c8"},"url":"https://jobsearcher.com/jobs/d5026c2f66fabeb3649857c8"}}