{"schemaVersion":"jobsearcher.job.v1","id":"82a636d8a7a253688a17eece","url":"https://jobsearcher.com/jobs/82a636d8a7a253688a17eece","canonicalUrl":"https://jobsearcher.com/jobs/82a636d8a7a253688a17eece","title":"Software Validation Engineer Remote Location","description":"Plymouth MNJob Description:>> Bachelors degree in Computer Science, Information Technology, Electronics Engineering, or a related field required>> Minimum 5-8 years of experience in software validation, preferably within the medical device, pharmaceutical, or regulated healthcare industries>> Strong understanding of software development lifecycle (SDLC) methodologies, validation planning, risk management, and quality assurance principles>> Experience in handling SW development and verification tools>> Good exposure to FDA regulations (21 CFR Part 11, Part 820), ISO 13485, EU MDR, GAMP 5, and other relevant standards for software lifecycle and validation>> Experience with computerized system validation (CSV) approaches for non-product applications>> Proficiency in authoring validation documents as per SOP or work instruction>> Responsible for SW Validation planning, requirement gathering, Risk assessment, protocol development and test execution>> Work with cross functional team and SME to understand the intended use and prepare the above documentationRequirements:>> Bachelors degree in Computer Science, Information Technology, Electronics Engineering, or a related field>> Minimum 5-8 years of experience in software validation, preferably within the medical device, pharmaceutical, or regulated healthcare industries>> Strong understanding of software development lifecycle (SDLC) methodologies, validation planning, risk management, and quality assurance principles>> Experience in handling SW development and verification tools>> Good exposure to FDA regulations (21 CFR Part 11, Part 820), ISO 13485, EU MDR, GAMP 5, and other relevant standards for software lifecycle and validation>> Experience with computerized system validation (CSV) approaches for non-product applications>> Proficiency in authoring validation documents as per SOP or work instruction","company":"Via Dice","rawCompany":"via dice","city":"Denver","state":"CO","isRemote":true,"isActive":false,"createdAt":"2026-08-14T12:10:52.769Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"15-1252.00","title":"Software Developers","slug":"software-developers"},{"code":"15-1253.00","title":"Software Quality Assurance Analysts and Testers","slug":"software-quality-assurance-analysts-and-testers"}],"industries":[{"code":"541512","title":"Computer Systems Design Services","slug":"computer-systems-design-services"},{"code":"541511","title":"Custom Computer Programming Services","slug":"custom-computer-programming-services"},{"code":"513210","title":"Software 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work instruction>> Responsible for SW Validation planning, requirement gathering, Risk assessment, protocol development and test execution>> Work with cross functional team and SME to understand the intended use and prepare the above documentationRequirements:>> Bachelors degree in Computer Science, Information Technology, Electronics Engineering, or a related field>> Minimum 5-8 years of experience in software validation, preferably within the medical device, pharmaceutical, or regulated healthcare industries>> Strong understanding of software development lifecycle (SDLC) methodologies, validation planning, risk management, and quality assurance principles>> Experience in handling SW development and verification tools>> Good exposure to FDA regulations (21 CFR Part 11, Part 820), ISO 13485, EU MDR, GAMP 5, and other relevant standards for software lifecycle and validation>> Experience with computerized system validation (CSV) approaches for non-product applications>> Proficiency in 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