{"schemaVersion":"jobsearcher.job.v1","id":"b1adc40371f8f8c4aea6c2a2","url":"https://jobsearcher.com/jobs/b1adc40371f8f8c4aea6c2a2","canonicalUrl":"https://jobsearcher.com/jobs/b1adc40371f8f8c4aea6c2a2","title":"Validation Engineer","description":"Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\r\nWe are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:\r\n\r\nValidation Engineer\r\n\r\nDescription\r\nThe role demands deep technical expertise across the full validation lifecycle including URS development, FAT/SAT execution, and Computer System Validation (CSV) as well as hands-on experience with systems and controls integration. The candidate will drive end-to-end project implementation: from equipment design and installation through startup, commissioning, and qualification.\r\nKey Responsibilities\r\n\r\nDevelop User Requirement Specifications (URS).\r\nLead full validation lifecycle activities: FAT, SAT, CSV, equipment integration, and startup.\r\nDrive process design for new equipment and ensure product design requirements are met.\r\nExecute commissioning and qualification activities for new and existing equipment.\r\nProvide technical oversight to ensure equipment meets safety, regulatory, and operational standards.\r\nManage suppliers and external vendors on capital projects, controlling scope, cost, and lead time.\r\nCollaborate with Procurement and Legal on vendor contracts.\r\nCreate and maintain engineering documentation (URS, assembly instructions, bill of process, etc.).\r\nOptimize equipment design for manufacturability, cost reduction, maintainability, and efficiency.\r\nLead design reviews, risk assessments, and FMEA to ensure reliability and performance.\r\nEnsure compliance with all safety regulations and quality policies, procedures, and GMP standards.\r\nApply statistical analysis and SPC systems to support data-driven decision-making.\r\nManage multiple priorities and maintain equipment qualification schedules.\r\n\r\nQualifications\r\n\r\nBachelor's degree in Engineering or Science.\r\nMinimum 4 years of engineering experience in pharmaceutical and/or medical device industries.\r\nDemonstrated experience across the full validation lifecycle (URS, FAT, SAT, CSV).\r\nProven track record supporting full project implementation: design, installation, startup, commissioning, and qualification.\r\nStrong experience executing capital projects within GMP-regulated manufacturing environments.\r\nFamiliarity with GMP, ISO standards, Lean Manufacturing, and FDA-regulated environments.\r\nAbility to work independently and lead solutions under general direction.\r\nStrong organization, and communication skills\r\n\r\nAt Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.\r\nExcited to build something meaningful together? We look forward to hearing from you.\r\nValidation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.","company":"Validation Engineering Group","rawCompany":"validation engineering group","city":"Greenville","state":"NC","isRemote":false,"isActive":false,"createdAt":"2026-06-11T14:07:13.386Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"17-2031.00","title":"Bioengineers and Biomedical Engineers","slug":"bioengineers-and-biomedical-engineers"}],"industries":[{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\r\nWe are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:\r\n\r\nValidation Engineer\r\n\r\nDescription\r\nThe role demands deep technical expertise across the full validation lifecycle including URS development, FAT/SAT execution, and Computer System Validation (CSV) as well as hands-on experience with systems and controls integration. The candidate will drive end-to-end project implementation: from equipment design and installation through startup, commissioning, and qualification.\r\nKey Responsibilities\r\n\r\nDevelop User Requirement Specifications (URS).\r\nLead full validation lifecycle activities: FAT, SAT, CSV, equipment integration, and startup.\r\nDrive process design for new equipment and ensure product design requirements are met.\r\nExecute commissioning and qualification activities for new and existing equipment.\r\nProvide technical oversight to ensure equipment meets safety, regulatory, and operational standards.\r\nManage suppliers and external vendors on capital projects, controlling scope, cost, and lead time.\r\nCollaborate with Procurement and Legal on vendor contracts.\r\nCreate and maintain engineering documentation (URS, assembly instructions, bill of process, etc.).\r\nOptimize equipment design for manufacturability, cost reduction, maintainability, and efficiency.\r\nLead design reviews, risk assessments, and FMEA to ensure reliability and performance.\r\nEnsure compliance with all safety regulations and quality policies, procedures, and GMP standards.\r\nApply statistical analysis and SPC systems to support data-driven decision-making.\r\nManage multiple priorities and maintain equipment qualification schedules.\r\n\r\nQualifications\r\n\r\nBachelor's degree in Engineering or Science.\r\nMinimum 4 years of engineering experience in pharmaceutical and/or medical device industries.\r\nDemonstrated experience across the full validation lifecycle (URS, FAT, SAT, CSV).\r\nProven track record supporting full project implementation: design, installation, startup, commissioning, and qualification.\r\nStrong experience executing capital projects within GMP-regulated manufacturing environments.\r\nFamiliarity with GMP, ISO standards, Lean Manufacturing, and FDA-regulated environments.\r\nAbility to work independently and lead solutions under general direction.\r\nStrong organization, and communication skills\r\n\r\nAt Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.\r\nExcited to build something meaningful together? We look forward to hearing from you.\r\nValidation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.","datePosted":"2026-06-11T14:07:13.386Z","dateModified":"2026-06-11T14:07:13.386Z","hiringOrganization":{"@type":"Organization","name":"Validation Engineering Group","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Greenville","addressRegion":"NC","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"b1adc40371f8f8c4aea6c2a2"},"url":"https://jobsearcher.com/jobs/b1adc40371f8f8c4aea6c2a2"}}