{"schemaVersion":"jobsearcher.job.v1","id":"f17cd21c1ea4f710ef5a0937","url":"https://jobsearcher.com/jobs/f17cd21c1ea4f710ef5a0937","canonicalUrl":"https://jobsearcher.com/jobs/f17cd21c1ea4f710ef5a0937","title":"Sterilization Program Manager- Ethylene Oxide (EO) (Remote Work)","description":"Summary:\nThe Sterilization Program Manager is responsible for leading and managing the sterilization project portfolio, including new product launches, validation and revalidation activities, process improvements, and operational support. This role provides technical oversight for Ethylene Oxide (EO) sterilization processes, drives cross-functional collaboration, manages supplier relationships, and ensures compliance with global sterilization regulations and standards.\n\nKey Responsibilities:\nProgram & Portfolio Management\nLead and manage the full sterilization project portfolio, including:\nNew product launches\nSterilization validations and revalidations\nProcess improvement initiatives\nDevelop and maintain integrated project plans, timelines, resource allocation plans, and risk registers.\nDrive alignment across cross-functional teams including R&D, Quality, Regulatory Affairs, Operations, and Supply Chain.\nFacilitate portfolio prioritization and support trade-off decisions with senior leadership.\nEstablish, monitor, and report key performance indicators (KPIs), project milestones, and program health metrics.\nTechnical Oversight\nServe as Subject Matter Expert (SME) for EO sterilization processes.\nProvide technical guidance related to microbiological and chemical sterilization methods.\nEnsure compliance with applicable international regulations, standards, and industry requirements.\nSupport technical problem-solving and troubleshooting efforts across sterilization-related activities.\nCollaborate with internal SMEs to resolve complex sterilization challenges.\nSterilization & Service Supplier Management\nCoordinate with internal stakeholders to manage relationships with contract sterilization providers and laboratory service vendors.\nSupport project scheduling and resource planning with external service suppliers.\nEnsure supplier activities align with project priorities, timelines, and business objectives.\nStakeholder & Change Management\nCommunicate project status, risks, mitigation plans, and key decisions to executive leadership and cross-functional teams.\nLead change control activities associated with sterilization process modifications.\nPromote continuous improvement initiatives and process optimization opportunities.\nDrive effective stakeholder engagement throughout the project lifecycle.\nRequirements\nBachelor’s Degree in:\nBiomedical Engineering\nChemical Engineering\nMicrobiology or related scientific/engineering discipline\nMinimum 3 years of experience in EO sterilization validation and/or sterilization operations.\nStrong knowledge of sterilization validation lifecycle activities.\nExperience supporting validation, compliance, and process improvement projects.\nPreferred Qualifications\nPMP Certification or equivalent project management certification.\nExperience in medical device, pharmaceutical, or regulated manufacturing environments.\nKnowledge of international sterilization standards and regulatory requirements.\nRequired Skills\nSterilization & Validation\nEO Sterilization Processes\nSterilization Validation Lifecycle\nRevalidation Activities\nMicrobiological Methods\nChemical Sterilization Methods\nRegulatory Compliance\nProgram Management\nPortfolio Management\nResource Planning\nProject Scheduling\nRisk Management\nFMEA\nRisk Registers\nKPI Development & Reporting\nCross-Functional Leadership\nSoftware & Tools\nMicrosoft Office Suite\nMicrosoft Project\nSmartsheet\nAgile Methodologies\nSoft Skills\nLeadership\nStrategic Planning\nStakeholder Management\nCommunication & Presentation Skills\nProblem Solving\nContinuous Improvement Mindset\nChange Management\nWork Methodology\nRemote work reporting to the Juncos, PR site.\nFull Time Job\nShift: Administrative Shift, but needs to be available for others.\nDuration: 1 year (with possible extension or conversion depending on project and performance).\nProfessional services Contract\nType of industry: Medical devices","company":"Cisinternationalllc","rawCompany":"cisinternationalllc","isRemote":true,"isActive":false,"createdAt":"2026-08-05T13:03:51.813Z","occupations":[{"code":"13-1082.00","title":"Project Management Specialists","slug":"project-management-specialists"},{"code":"11-9041.00","title":"Architectural and Engineering Managers","slug":"architectural-and-engineering-managers"},{"code":"11-9121.00","title":"Natural Sciences Managers","slug":"natural-sciences-managers"}],"industries":[{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"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 Program Manager- Ethylene Oxide (EO) (Remote Work)","description":"Summary:\nThe Sterilization Program Manager is responsible for leading and managing the sterilization project portfolio, including new product launches, validation and revalidation activities, process improvements, and operational support. This role provides technical oversight for Ethylene Oxide (EO) sterilization processes, drives cross-functional collaboration, manages supplier relationships, and ensures compliance with global sterilization regulations and standards.\n\nKey Responsibilities:\nProgram & Portfolio Management\nLead and manage the full sterilization project portfolio, including:\nNew product launches\nSterilization validations and revalidations\nProcess improvement initiatives\nDevelop and maintain integrated project plans, timelines, resource allocation plans, and risk registers.\nDrive alignment across cross-functional teams including R&D, Quality, Regulatory Affairs, Operations, and Supply Chain.\nFacilitate portfolio prioritization and support trade-off decisions with senior leadership.\nEstablish, monitor, and report key performance indicators (KPIs), project milestones, and program health metrics.\nTechnical Oversight\nServe as Subject Matter Expert (SME) for EO sterilization processes.\nProvide technical guidance related to microbiological and chemical sterilization methods.\nEnsure compliance with applicable international regulations, standards, and industry requirements.\nSupport technical problem-solving and troubleshooting efforts across sterilization-related activities.\nCollaborate with internal SMEs to resolve complex sterilization challenges.\nSterilization & Service Supplier Management\nCoordinate with internal stakeholders to manage relationships with contract sterilization providers and laboratory service vendors.\nSupport project scheduling and resource planning with external service suppliers.\nEnsure supplier activities align with project priorities, timelines, and business objectives.\nStakeholder & Change Management\nCommunicate project status, risks, mitigation plans, and key decisions to executive leadership and cross-functional teams.\nLead change control activities associated with sterilization process modifications.\nPromote continuous improvement initiatives and process optimization opportunities.\nDrive effective stakeholder engagement throughout the project lifecycle.\nRequirements\nBachelor’s Degree in:\nBiomedical Engineering\nChemical Engineering\nMicrobiology or related scientific/engineering discipline\nMinimum 3 years of experience in EO sterilization validation and/or sterilization operations.\nStrong knowledge of sterilization validation lifecycle activities.\nExperience supporting validation, compliance, and process improvement projects.\nPreferred Qualifications\nPMP Certification or equivalent project management certification.\nExperience in medical device, pharmaceutical, or regulated manufacturing environments.\nKnowledge of international sterilization standards and regulatory requirements.\nRequired Skills\nSterilization & Validation\nEO Sterilization Processes\nSterilization Validation Lifecycle\nRevalidation Activities\nMicrobiological Methods\nChemical Sterilization Methods\nRegulatory Compliance\nProgram Management\nPortfolio Management\nResource Planning\nProject Scheduling\nRisk Management\nFMEA\nRisk Registers\nKPI Development & Reporting\nCross-Functional Leadership\nSoftware & Tools\nMicrosoft Office Suite\nMicrosoft Project\nSmartsheet\nAgile Methodologies\nSoft Skills\nLeadership\nStrategic Planning\nStakeholder Management\nCommunication & Presentation Skills\nProblem Solving\nContinuous Improvement Mindset\nChange Management\nWork Methodology\nRemote work reporting to the Juncos, PR site.\nFull Time Job\nShift: Administrative Shift, but needs to be available for others.\nDuration: 1 year (with possible extension or conversion depending on project and performance).\nProfessional services Contract\nType of industry: Medical devices","datePosted":"2026-08-05T13:03:51.813Z","dateModified":"2026-08-05T13:03:51.813Z","hiringOrganization":{"@type":"Organization","name":"Cisinternationalllc","sameAs":"https://jobsearcher.com"},"jobLocationType":"TELECOMMUTE","applicantLocationRequirements":{"@type":"Country","name":"US"},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"f17cd21c1ea4f710ef5a0937"},"url":"https://jobsearcher.com/jobs/f17cd21c1ea4f710ef5a0937"}}