{"schemaVersion":"jobsearcher.job.v1","id":"78f6337f87e0636498dce7aa","url":"https://jobsearcher.com/jobs/78f6337f87e0636498dce7aa","canonicalUrl":"https://jobsearcher.com/jobs/78f6337f87e0636498dce7aa","title":"Senior Validation Engineer","description":"Job Summary:\nWe are seeking an experienced Senior Validation Engineer / Senior CQV Engineer to support commissioning, qualification, and validation activities for equipment, systems, software, and manufacturing processes. The ideal candidate will have strong experience authoring, reviewing, and executing CQV documentation and test protocols in a regulated environment. This role will also involve hands-on testing of automated manufacturing or packaging equipment.\nRoles and Responsibilities:\nAuthor, edit, review, and execute commissioning, qualification, and validation documentation.\nExecute test scripts and accurately document test results and observations.\nMaintain clear, detailed, and GMP-compliant qualification and validation records.\nComplete assigned validation and qualification activities according to project schedules.\nRead and interpret technical schematics and equipment documentation.\nIdentify and test photo sensors, verify part numbers, and perform I/O testing on automated manufacturing equipment.\nSupport qualification and testing activities for equipment, systems, software, and manufacturing processes.\nCollaborate effectively with project leaders and cross-functional teams.\nFollow GMP and Good Documentation Practices (GDP) requirements.\nEducation and Experience:\nBachelor's Degree or equivalent experience.\n5+ years of experience in commissioning, qualification, validation, or related testing activities.\nStrong experience authoring and executing technical CQV documentation and protocols.\nExperience executing test scripts and documenting results.\nAbility to read and understand technical schematics.\nStrong problem-solving, organizational, and attention-to-detail skills.\nExcellent verbal and written communication skills.\nAbility to work effectively both independently and as part of a team.\nProficiency in Microsoft Word, Excel, and PowerPoint.\nPreferred Qualifications:\nExperience supporting packaging equipment or packaging line qualification and validation.\nExperience in pharmaceutical, medical device, combination product, or other regulated manufacturing environments.","company":"Katalysthealthcares","rawCompany":"katalysthealthcares","city":"Bloomington","state":"IL","isRemote":false,"isActive":false,"createdAt":"2026-09-16T10:12:20.960Z","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":"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":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Senior Validation Engineer","description":"Job Summary:\nWe are seeking an experienced Senior Validation Engineer / Senior CQV Engineer to support commissioning, qualification, and validation activities for equipment, systems, software, and manufacturing processes. The ideal candidate will have strong experience authoring, reviewing, and executing CQV documentation and test protocols in a regulated environment. This role will also involve hands-on testing of automated manufacturing or packaging equipment.\nRoles and Responsibilities:\nAuthor, edit, review, and execute commissioning, qualification, and validation documentation.\nExecute test scripts and accurately document test results and observations.\nMaintain clear, detailed, and GMP-compliant qualification and validation records.\nComplete assigned validation and qualification activities according to project schedules.\nRead and interpret technical schematics and equipment documentation.\nIdentify and test photo sensors, verify part numbers, and perform I/O testing on automated manufacturing equipment.\nSupport qualification and testing activities for equipment, systems, software, and manufacturing processes.\nCollaborate effectively with project leaders and cross-functional teams.\nFollow GMP and Good Documentation Practices (GDP) requirements.\nEducation and Experience:\nBachelor's Degree or equivalent experience.\n5+ years of experience in commissioning, qualification, validation, or related testing activities.\nStrong experience authoring and executing technical CQV documentation and protocols.\nExperience executing test scripts and documenting results.\nAbility to read and understand technical schematics.\nStrong problem-solving, organizational, and attention-to-detail skills.\nExcellent verbal and written communication skills.\nAbility to work effectively both independently and as part of a team.\nProficiency in Microsoft Word, Excel, and PowerPoint.\nPreferred Qualifications:\nExperience supporting packaging equipment or packaging line qualification and validation.\nExperience in pharmaceutical, medical device, combination product, or other regulated manufacturing environments.","datePosted":"2026-09-16T10:12:20.960Z","dateModified":"2026-09-16T10:12:20.960Z","hiringOrganization":{"@type":"Organization","name":"Katalysthealthcares","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bloomington","addressRegion":"IL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"78f6337f87e0636498dce7aa"},"url":"https://jobsearcher.com/jobs/78f6337f87e0636498dce7aa"}}