{"schemaVersion":"jobsearcher.job.v1","id":"9f730c9b0e547a3a8a6ae201","url":"https://jobsearcher.com/jobs/9f730c9b0e547a3a8a6ae201","canonicalUrl":"https://jobsearcher.com/jobs/9f730c9b0e547a3a8a6ae201","title":"Sterilization Validation - CQV Engineer","description":"*Position Summary*\nThe Sterilization Validation/CQV Engineer will support development and execution of sterilization qualification activities involving autoclaves, SIP systems, thermometric studies, Biological Indicators, and associated sterilization cycles.\n\n*Key Responsibilities*\n\n* Develop and execute Sterilization PQ protocols.\n* Prepare the corresponding Sterilization PQ final reports.\n* Review existing and new autoclave cycles and load configurations.\n* Support the qualification of new or modified sterilization cycles.\n* Coordinate thermometric studies, including thermocouple and Biological Indicator placement and retrieval.\n* Review temperature profiles, exposure times, lethality calculations, and other applicable cycle parameters.\n* Evaluate sterilization cycle results against approved protocol acceptance criteria.\n* Support sterilization conditional release activities as required.\n* Review SIP cycles, when applicable.\n* Generate and review PI Historian trends.\n* Identify and communicate any nonconforming or unexpected sterilization results.\n* Support investigations and technical assessments related to execution issues or discrepancies.\n* Coordinate execution activities with Manufacturing, Engineering, QC/Microbiology, and Quality.\n* Provide execution support during off-shifts, weekends, and extended-hour activities based on project needs.\n* Review sterilization calculations, data, and execution results as required.\n\n*Minimum Recommended Qualifications*\n\n* Bachelor's degree in Engineering, Microbiology, Biotechnology, Life Sciences, or a related field.\n* At least 5 years of experience in validation within the pharmaceutical or biotechnology industry.\n* At least 3 years of experience supporting sterilization validation activities.\n* Hands-on experience with autoclave qualification.\n* Experience with thermometric studies and the use of Biological Indicators.\n* Knowledge of SIP systems and sterilization cycle parameters.\n\n\\*Weil Group is proud to be an Equal Employment Opportunity Employer.\\*\n\n#IND2\n\nEducation:\n* Bachelor's (Required)\n\nExperience:\n* validation: 5 years (Required)\n* Sterilization Validation: 5 years (Preferred)\n\nWork Location: In person","company":"Weil Group","rawCompany":"weil group","city":"Juncos","state":"PR","isRemote":false,"isActive":false,"createdAt":"2026-09-06T14:00:58.305Z","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":"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":"Sterilization Validation - CQV Engineer","description":"*Position Summary*\nThe Sterilization Validation/CQV Engineer will support development and execution of sterilization qualification activities involving autoclaves, SIP systems, thermometric studies, Biological Indicators, and associated sterilization cycles.\n\n*Key Responsibilities*\n\n* Develop and execute Sterilization PQ protocols.\n* Prepare the corresponding Sterilization PQ final reports.\n* Review existing and new autoclave cycles and load configurations.\n* Support the qualification of new or modified sterilization cycles.\n* Coordinate thermometric studies, including thermocouple and Biological Indicator placement and retrieval.\n* Review temperature profiles, exposure times, lethality calculations, and other applicable cycle parameters.\n* Evaluate sterilization cycle results against approved protocol acceptance criteria.\n* Support sterilization conditional release activities as required.\n* Review SIP cycles, when applicable.\n* Generate and review PI Historian trends.\n* Identify and communicate any nonconforming or unexpected sterilization results.\n* Support investigations and technical assessments related to execution issues or discrepancies.\n* Coordinate execution activities with Manufacturing, Engineering, QC/Microbiology, and Quality.\n* Provide execution support during off-shifts, weekends, and extended-hour activities based on project needs.\n* Review sterilization calculations, data, and execution results as required.\n\n*Minimum Recommended Qualifications*\n\n* Bachelor's degree in Engineering, Microbiology, Biotechnology, Life Sciences, or a related field.\n* At least 5 years of experience in validation within the pharmaceutical or biotechnology industry.\n* At least 3 years of experience supporting sterilization validation activities.\n* Hands-on experience with autoclave qualification.\n* Experience with thermometric studies and the use of Biological Indicators.\n* Knowledge of SIP systems and sterilization cycle parameters.\n\n\\*Weil Group is proud to be an Equal Employment Opportunity Employer.\\*\n\n#IND2\n\nEducation:\n* Bachelor's (Required)\n\nExperience:\n* validation: 5 years (Required)\n* Sterilization Validation: 5 years (Preferred)\n\nWork Location: In person","datePosted":"2026-09-06T14:00:58.305Z","dateModified":"2026-09-06T14:00:58.305Z","hiringOrganization":{"@type":"Organization","name":"Weil Group","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Juncos","addressRegion":"PR","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"9f730c9b0e547a3a8a6ae201"},"url":"https://jobsearcher.com/jobs/9f730c9b0e547a3a8a6ae201"}}