{"schemaVersion":"jobsearcher.job.v1","id":"9a87623f27dc7a51e006fb82","url":"https://jobsearcher.com/jobs/9a87623f27dc7a51e006fb82","canonicalUrl":"https://jobsearcher.com/jobs/9a87623f27dc7a51e006fb82","title":"Senior Validation Engineer","description":"Review, analyze, and continuously improve the Cleaning Validation Program.\nGenerate and maintain relevant Standard Operating Procedures (SOPs).\nAssess Cleaning Validation Observations from the FDA, compiling and analyzing data to identify recurring issues in pharmaceutical and biopharmaceutical companies.\nPrepare a comprehensive plan to address observed issues based on current regulatory expectations.\nPresent findings to clients, showcasing the potential support that Validation Consulting Group LLC can provide to resolve common Cleaning Validation compliance issues.\nProvide laboratory support for Cleaning Process Validation through CPCI.\nSupport the introduction of new products and conduct relevant cleaning assessments.\nAssist with the calculation of cleaning validation acceptance criteria.\nSupport the determination of worst-case soil scenarios.\nDevelop and implement a Visual Inspection Program for clients who lack such systems, which includes:\nSOP for visual inspection\nTraining SOP and materials for the pharmaceutical, biopharmaceutical, and medical device industries.\nPresentation of the approach at relevant conferences.\nExploration of camera usage for post-use cleaning validation, including comprehensive research on existing camera technologies and the identification of new types suitable for inspecting manufacturing equipment.\nIdentification of technologies to ensure the Visual Inspection Program operates independently of personnel.\nQualifications:\nA Master’s degree in a relevant field is required, along with a minimum of 4 years of professional experience in the pharmaceutical or biopharmaceutical industries.\nAn extensive understanding of validation concepts, particularly cleaning and sterilization validation, is a must.\nCandidates should have up-to-date knowledge of current regulatory standards.\nExperience in defending during inspections is highly preferred.\nKnowledge of biopharmaceutical processes and requirements is an advantage.\nJob Type: Part-time\nPay: $35,000.00 - $40,000.00 per year\nSchedule:\n4 hour shift\nWork Location: Remote","company":"Validation Group","rawCompany":"validation group","city":"Remote","state":"OR","isRemote":false,"isActive":false,"createdAt":"2026-08-10T13:07:49.277Z","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":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Senior Validation Engineer","description":"Review, analyze, and continuously improve the Cleaning Validation Program.\nGenerate and maintain relevant Standard Operating Procedures (SOPs).\nAssess Cleaning Validation Observations from the FDA, compiling and analyzing data to identify recurring issues in pharmaceutical and biopharmaceutical companies.\nPrepare a comprehensive plan to address observed issues based on current regulatory expectations.\nPresent findings to clients, showcasing the potential support that Validation Consulting Group LLC can provide to resolve common Cleaning Validation compliance issues.\nProvide laboratory support for Cleaning Process Validation through CPCI.\nSupport the introduction of new products and conduct relevant cleaning assessments.\nAssist with the calculation of cleaning validation acceptance criteria.\nSupport the determination of worst-case soil scenarios.\nDevelop and implement a Visual Inspection Program for clients who lack such systems, which includes:\nSOP for visual inspection\nTraining SOP and materials for the pharmaceutical, biopharmaceutical, and medical device industries.\nPresentation of the approach at relevant conferences.\nExploration of camera usage for post-use cleaning validation, including comprehensive research on existing camera technologies and the identification of new types suitable for inspecting manufacturing equipment.\nIdentification of technologies to ensure the Visual Inspection Program operates independently of personnel.\nQualifications:\nA Master’s degree in a relevant field is required, along with a minimum of 4 years of professional experience in the pharmaceutical or biopharmaceutical industries.\nAn extensive understanding of validation concepts, particularly cleaning and sterilization validation, is a must.\nCandidates should have up-to-date knowledge of current regulatory standards.\nExperience in defending during inspections is highly preferred.\nKnowledge of biopharmaceutical processes and requirements is an advantage.\nJob Type: Part-time\nPay: $35,000.00 - $40,000.00 per year\nSchedule:\n4 hour shift\nWork Location: Remote","datePosted":"2026-08-10T13:07:49.277Z","dateModified":"2026-08-10T13:07:49.277Z","hiringOrganization":{"@type":"Organization","name":"Validation Group","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Remote","addressRegion":"OR","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"9a87623f27dc7a51e006fb82"},"url":"https://jobsearcher.com/jobs/9a87623f27dc7a51e006fb82"}}