{"schemaVersion":"jobsearcher.job.v1","id":"d0f17e2a81f032d4ebf8f6de","url":"https://jobsearcher.com/jobs/d0f17e2a81f032d4ebf8f6de","canonicalUrl":"https://jobsearcher.com/jobs/d0f17e2a81f032d4ebf8f6de","title":"Validation Manager","description":"Must Haves:\nMust be from Pharmaceutical Background\nMust have Sterile injectable experience\nMinimum 5 years in a management role in Validation in pharmaceutical industry.\nValidation Master Plan Development / Update – VMP, CVMP\nDevelop and write applicable validation documentation, including, but limited to URSs, FDSs, DOEs, FATs, IQs, OQs, PQs, VQs\nValidation of: Autoclaves, Depyrogenation Tunnels, Stability / Incubator / Refrigeration Chambers, Cleaning Equipment / Processes, Analytical Instruments, Facilities, Media Fills, Smoke Studies, Kaye Instrumentation\nKnowledge of cGMP requirements on validation methods and principals including FDA, ISPE, GAMP guidelines and FDA, CFR Part 11\nPosition Summary:\nProvide expertise, guidance, and oversight for the Validation efforts at Rising Facility. Ensure the development and implementation of the Rising Validation Department and the Site Validation Master Plan. Effectively oversee industry \"best practices\" using resources, such as ISPE and PDA and continuously upgrade the Site's validation practices and procedures. Manage site compliance with current FDA regulatory requirements and expertise to work with all levels of management, staff, and internal departments including outside contractors and vendors, as applicable.\nJob Type: Full-time\nPay: $120,503.00 - $122,731.00 per year\nBenefits:\n401(k)\n401(k) matching\nDental insurance\nHealth insurance\nLife insurance\nPaid time off\nVision insurance\nSchedule:\n8 hour shift\nEducation:\nBachelor's (Preferred)\nExperience:\nSterile Injectables: 3 years (Required)\nWork Location: In person","company":"Hiresigm","rawCompany":"hiresigm","city":"Decatur","state":"IL","isRemote":false,"isActive":false,"createdAt":"2026-04-12T21:21:09.351Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"11-9199.01","title":"Regulatory Affairs Managers","slug":"regulatory-affairs-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":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Manager","description":"Must Haves:\nMust be from Pharmaceutical Background\nMust have Sterile injectable experience\nMinimum 5 years in a management role in Validation in pharmaceutical industry.\nValidation Master Plan Development / Update – VMP, CVMP\nDevelop and write applicable validation documentation, including, but limited to URSs, FDSs, DOEs, FATs, IQs, OQs, PQs, VQs\nValidation of: Autoclaves, Depyrogenation Tunnels, Stability / Incubator / Refrigeration Chambers, Cleaning Equipment / Processes, Analytical Instruments, Facilities, Media Fills, Smoke Studies, Kaye Instrumentation\nKnowledge of cGMP requirements on validation methods and principals including FDA, ISPE, GAMP guidelines and FDA, CFR Part 11\nPosition Summary:\nProvide expertise, guidance, and oversight for the Validation efforts at Rising Facility. Ensure the development and implementation of the Rising Validation Department and the Site Validation Master Plan. Effectively oversee industry \"best practices\" using resources, such as ISPE and PDA and continuously upgrade the Site's validation practices and procedures. Manage site compliance with current FDA regulatory requirements and expertise to work with all levels of management, staff, and internal departments including outside contractors and vendors, as applicable.\nJob Type: Full-time\nPay: $120,503.00 - $122,731.00 per year\nBenefits:\n401(k)\n401(k) matching\nDental insurance\nHealth insurance\nLife insurance\nPaid time off\nVision insurance\nSchedule:\n8 hour shift\nEducation:\nBachelor's (Preferred)\nExperience:\nSterile Injectables: 3 years (Required)\nWork Location: In person","datePosted":"2026-04-12T21:21:09.351Z","dateModified":"2026-04-12T21:21:09.351Z","hiringOrganization":{"@type":"Organization","name":"Hiresigm","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Decatur","addressRegion":"IL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"d0f17e2a81f032d4ebf8f6de"},"url":"https://jobsearcher.com/jobs/d0f17e2a81f032d4ebf8f6de"}}