{"schemaVersion":"jobsearcher.job.v1","id":"87b6755f2f72f8b6cef6997d","url":"https://jobsearcher.com/jobs/87b6755f2f72f8b6cef6997d","canonicalUrl":"https://jobsearcher.com/jobs/87b6755f2f72f8b6cef6997d","title":"Technical Program Manager","description":"**UNFORTUNATELY UNABLE TO WORK WITH VISAS OR TO SUBCONTRACT**Seeking a Technical Program Manager who will be responsible for driving alignment, accountability, planning, risk management, governance, and execution across a cross-functional global organization in the development of medical devices. The role requires a strong leader who can operate at both strategic and operational levels, ensuring that technical decisions, business objectives, regulatory requirements, and commercialization plans remain aligned throughout the program lifecycle.Responsibilities:Leading teams through all phases of product development, regulatory submission, launch readiness, commercialization, and post-launch transition.Ensuring all phase deliverables, reviews, design controls, and development artifacts are completed on time and with a high degree of quality.Partner with Quality and Regulatory teams to ensure compliance with applicable medical device standards and regulations.Lead launch planning across R&D, Operations, Commercial, Service, Marketing, Training, and Supply Chain organizationsProvide regular executive-level communication on program status, risks, financial implications, and mitigation plans.Lead program reviews, governance forums, and executive decision-making processes.Requirements:Bachelor’s degree in engineering, Biomedical Engineering, Computer Science, or related technical discipline.10+ years of progressively increasing responsibility in Program Management, Product Development, or Engineering Leadership.Proven experience leading complex medical device, digital health, connected device, or Software as a Medical Device (SaMD) program.Demonstrated experience delivering products from development through regulatory approval, launch, and commercialization.Strong understanding of medical device product development processes, design controls, risk management, and regulatory requirements.","company":"Integrity Consulting","rawCompany":"integrity consulting","city":"Dublin","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-08-28T08:08:16.934Z","occupations":[{"code":"13-1082.00","title":"Project Management Specialists","slug":"project-management-specialists"},{"code":"15-1299.09","title":"Information Technology Project Managers","slug":"information-technology-project-managers"},{"code":"11-9041.00","title":"Architectural and Engineering Managers","slug":"architectural-and-engineering-managers"}],"industries":[{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Technical Program Manager","description":"**UNFORTUNATELY UNABLE TO WORK WITH VISAS OR TO SUBCONTRACT**Seeking a Technical Program Manager who will be responsible for driving alignment, accountability, planning, risk management, governance, and execution across a cross-functional global organization in the development of medical devices. The role requires a strong leader who can operate at both strategic and operational levels, ensuring that technical decisions, business objectives, regulatory requirements, and commercialization plans remain aligned throughout the program lifecycle.Responsibilities:Leading teams through all phases of product development, regulatory submission, launch readiness, commercialization, and post-launch transition.Ensuring all phase deliverables, reviews, design controls, and development artifacts are completed on time and with a high degree of quality.Partner with Quality and Regulatory teams to ensure compliance with applicable medical device standards and regulations.Lead launch planning across R&D, Operations, Commercial, Service, Marketing, Training, and Supply Chain organizationsProvide regular executive-level communication on program status, risks, financial implications, and mitigation plans.Lead program reviews, governance forums, and executive decision-making processes.Requirements:Bachelor’s degree in engineering, Biomedical Engineering, Computer Science, or related technical discipline.10+ years of progressively increasing responsibility in Program Management, Product Development, or Engineering Leadership.Proven experience leading complex medical device, digital health, connected device, or Software as a Medical Device (SaMD) program.Demonstrated experience delivering products from development through regulatory approval, launch, and commercialization.Strong understanding of medical device product development processes, design controls, risk management, and regulatory requirements.","datePosted":"2026-08-28T08:08:16.934Z","dateModified":"2026-08-28T08:08:16.934Z","hiringOrganization":{"@type":"Organization","name":"Integrity Consulting","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Dublin","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"87b6755f2f72f8b6cef6997d"},"url":"https://jobsearcher.com/jobs/87b6755f2f72f8b6cef6997d"}}