{"schemaVersion":"jobsearcher.job.v1","id":"694b14a4d269768c494bb6b5","url":"https://jobsearcher.com/jobs/694b14a4d269768c494bb6b5","canonicalUrl":"https://jobsearcher.com/jobs/694b14a4d269768c494bb6b5","title":"Computer System Validation Engineer","description":"Job Title: Validation EngineerLocation: Indianapolis / Bloomington, IN (100% Onsite)Duration: Long term ContractInterview Mode: Onsite (Local candidates preferred)Job SummaryWe are seeking a Validation Engineer with strong experience in Computer Systems Validation (CSV), equipment qualification, and GMP-regulated environments. The ideal candidate will support validation activities, documentation migration, and equipment qualification to ensure compliance with regulatory standards.Key ResponsibilitiesLead migration of legacy validation documents into the Kneat digital platform, ensuring accuracy and compliancePerform equipment qualification for lab instruments (pH meters, thermal mixers, peristaltic pumps, nutating mixers, etc.)Execute temperature mapping studies, including work with Ellab systems or similar equipmentSupport Computer Systems Validation (CSV) activities and documentationAssist Process Engineering teams to ensure project timelines and milestones are metEnsure all validation activities comply with GMP and regulatory requirementsMaintain clear, accurate, and compliant documentationRequired QualificationsBachelor s degree in Engineering, Science, or related field6+ years of experience in Computer Systems Validation (CSV)4+ years of experience in pharmaceutical manufacturing environmentHands-on experience with equipment qualification and validationStrong knowledge of CSV principles and regulatory complianceExperience working in onsite, fast-paced environments","company":"Stark Pharma","rawCompany":"stark pharma","city":"Indianapolis","state":"IN","isRemote":false,"isActive":false,"createdAt":"2026-04-30T13:04:01.521Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-3028.00","title":"Calibration Technologists and Technicians","slug":"calibration-technologists-and-technicians"},{"code":"15-1299.08","title":"Computer Systems Engineers/Architects","slug":"computer-systems-engineers-architects"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-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"},{"code":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Computer System Validation Engineer","description":"Job Title: Validation EngineerLocation: Indianapolis / Bloomington, IN (100% Onsite)Duration: Long term ContractInterview Mode: Onsite (Local candidates preferred)Job SummaryWe are seeking a Validation Engineer with strong experience in Computer Systems Validation (CSV), equipment qualification, and GMP-regulated environments. The ideal candidate will support validation activities, documentation migration, and equipment qualification to ensure compliance with regulatory standards.Key ResponsibilitiesLead migration of legacy validation documents into the Kneat digital platform, ensuring accuracy and compliancePerform equipment qualification for lab instruments (pH meters, thermal mixers, peristaltic pumps, nutating mixers, etc.)Execute temperature mapping studies, including work with Ellab systems or similar equipmentSupport Computer Systems Validation (CSV) activities and documentationAssist Process Engineering teams to ensure project timelines and milestones are metEnsure all validation activities comply with GMP and regulatory requirementsMaintain clear, accurate, and compliant documentationRequired QualificationsBachelor s degree in Engineering, Science, or related field6+ years of experience in Computer Systems Validation (CSV)4+ years of experience in pharmaceutical manufacturing environmentHands-on experience with equipment qualification and validationStrong knowledge of CSV principles and regulatory complianceExperience working in onsite, fast-paced environments","datePosted":"2026-04-30T13:04:01.521Z","dateModified":"2026-04-30T13:04:01.521Z","hiringOrganization":{"@type":"Organization","name":"Stark Pharma","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Indianapolis","addressRegion":"IN","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"694b14a4d269768c494bb6b5"},"url":"https://jobsearcher.com/jobs/694b14a4d269768c494bb6b5"}}