{"schemaVersion":"jobsearcher.job.v1","id":"f1d19c2b19d7ae442b70dabc","url":"https://jobsearcher.com/jobs/f1d19c2b19d7ae442b70dabc","canonicalUrl":"https://jobsearcher.com/jobs/f1d19c2b19d7ae442b70dabc","title":"Validation Engineer","description":"We are seeking an experienced Validation Engineer to support commissioning, qualification, and computer system validation activities within a cGMP biopharmaceutical manufacturing environment. The ideal candidate will manage validation projects from concept through performance qualification while ensuring regulatory compliance and supporting manufacturing operations.Key Responsibilities:• Lead equipment, utility, facility, and computer system validation projects from planning through execution.• Author, review, and execute IQ/OQ/PQ protocols, validation reports, and lifecycle documentation.• Support Commissioning & Qualification (C&Q) and Computer System Validation (CSV) activities.• Validate bulk drug substance manufacturing equipment in single-use facilities.• Review URS, FS, DS, commissioning documents, and validation deliverables.• Support process improvements, temperature mapping, and compliance with cGMP/GxP requirements.• Collaborate with Engineering, Manufacturing, MSAT, QA, and cross-functional teams to ensure successful project execution.Required Qualifications:• Bachelor's degree in Engineering, Science, or a related field.• 5+ years of validation experience in biopharmaceutical or biotech manufacturing.• Strong experience with equipment qualification, CSV, IQ/OQ/PQ, and process validation.• Knowledge of cGMP, GxP, validation lifecycle, and regulatory requirements.• Experience with DeltaV, LIMS, MES, or similar validated systems preferred.• Excellent technical writing, communication, and problem-solving skills.","company":"United Pharma","rawCompany":"united pharma","city":"Wilton","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-08-05T09:03:36.093Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"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":"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":"Validation Engineer","description":"We are seeking an experienced Validation Engineer to support commissioning, qualification, and computer system validation activities within a cGMP biopharmaceutical manufacturing environment. The ideal candidate will manage validation projects from concept through performance qualification while ensuring regulatory compliance and supporting manufacturing operations.Key Responsibilities:• Lead equipment, utility, facility, and computer system validation projects from planning through execution.• Author, review, and execute IQ/OQ/PQ protocols, validation reports, and lifecycle documentation.• Support Commissioning & Qualification (C&Q) and Computer System Validation (CSV) activities.• Validate bulk drug substance manufacturing equipment in single-use facilities.• Review URS, FS, DS, commissioning documents, and validation deliverables.• Support process improvements, temperature mapping, and compliance with cGMP/GxP requirements.• Collaborate with Engineering, Manufacturing, MSAT, QA, and cross-functional teams to ensure successful project execution.Required Qualifications:• Bachelor's degree in Engineering, Science, or a related field.• 5+ years of validation experience in biopharmaceutical or biotech manufacturing.• Strong experience with equipment qualification, CSV, IQ/OQ/PQ, and process validation.• Knowledge of cGMP, GxP, validation lifecycle, and regulatory requirements.• Experience with DeltaV, LIMS, MES, or similar validated systems preferred.• Excellent technical writing, communication, and problem-solving skills.","datePosted":"2026-08-05T09:03:36.093Z","dateModified":"2026-08-05T09:03:36.093Z","hiringOrganization":{"@type":"Organization","name":"United Pharma","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Wilton","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"f1d19c2b19d7ae442b70dabc"},"url":"https://jobsearcher.com/jobs/f1d19c2b19d7ae442b70dabc"}}