{"schemaVersion":"jobsearcher.job.v1","id":"9ba77e6e24dcbb68a59dab74","url":"https://jobsearcher.com/jobs/9ba77e6e24dcbb68a59dab74","canonicalUrl":"https://jobsearcher.com/jobs/9ba77e6e24dcbb68a59dab74","title":"Senior Cell Therapy Process Validation Engineer","description":"Orca Bio, a Sacramento-based cell therapy company, seeks a Senior Process Validation Engineer to own PPQ campaigns and validate processes across manufacturing and shipping. You will collaborate with MSAT, CMC, QA, and Supply Chain to maintain validated states for cell therapy products.\nYou will author and review PVMP-related documents, support APS activities, and drive CAPA investigations while ensuring compliance with FDA/EMA standards and GMP requirements.\n\n#J-18808-Ljbffr","company":"Medium","rawCompany":"medium","city":"Sacramento","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-08-18T03:51:38.279Z","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":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Senior Cell Therapy Process Validation Engineer","description":"Orca Bio, a Sacramento-based cell therapy company, seeks a Senior Process Validation Engineer to own PPQ campaigns and validate processes across manufacturing and shipping. You will collaborate with MSAT, CMC, QA, and Supply Chain to maintain validated states for cell therapy products.\nYou will author and review PVMP-related documents, support APS activities, and drive CAPA investigations while ensuring compliance with FDA/EMA standards and GMP requirements.\n\n#J-18808-Ljbffr","datePosted":"2026-08-18T03:51:38.279Z","dateModified":"2026-08-18T03:51:38.279Z","hiringOrganization":{"@type":"Organization","name":"Medium","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Sacramento","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"9ba77e6e24dcbb68a59dab74"},"url":"https://jobsearcher.com/jobs/9ba77e6e24dcbb68a59dab74"}}