{"schemaVersion":"jobsearcher.job.v1","id":"88153241de8ea4d9f6567b95","url":"https://jobsearcher.com/jobs/88153241de8ea4d9f6567b95","canonicalUrl":"https://jobsearcher.com/jobs/88153241de8ea4d9f6567b95","title":"Lead CSV Specialist (Computer Systems Validation)","description":"A leading biopharma firm located in Indiana is seeking a Validation Associate II to support the Computer Systems Validation team. The successful candidate will work with IT and ensure compliance with industry best practices. Responsibilities include authoring validation documents, coordinating user access reviews, and participating in audits. Ideal candidates should have a bachelor's degree in a relevant field and experience in regulated environments. Competitive benefits and a collaborative work environment are offered.\r\nJ-18808-Ljbffr","company":"Simtra Us","rawCompany":"simtra us","city":"Bloomington","state":"IN","isRemote":false,"isActive":false,"createdAt":"2026-04-24T04:36:25.175Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"15-1211.00","title":"Computer Systems Analysts","slug":"computer-systems-analysts"},{"code":"13-1041.07","title":"Regulatory Affairs Specialists","slug":"regulatory-affairs-specialists"}],"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":"Lead CSV Specialist (Computer Systems Validation)","description":"A leading biopharma firm located in Indiana is seeking a Validation Associate II to support the Computer Systems Validation team. The successful candidate will work with IT and ensure compliance with industry best practices. Responsibilities include authoring validation documents, coordinating user access reviews, and participating in audits. Ideal candidates should have a bachelor's degree in a relevant field and experience in regulated environments. Competitive benefits and a collaborative work environment are offered.\r\nJ-18808-Ljbffr","datePosted":"2026-04-24T04:36:25.175Z","dateModified":"2026-04-24T04:36:25.175Z","hiringOrganization":{"@type":"Organization","name":"Simtra Us","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bloomington","addressRegion":"IN","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"88153241de8ea4d9f6567b95"},"url":"https://jobsearcher.com/jobs/88153241de8ea4d9f6567b95"}}