{"schemaVersion":"jobsearcher.job.v1","id":"b7fd41f8767eb8402a097b0d","url":"https://jobsearcher.com/jobs/b7fd41f8767eb8402a097b0d","canonicalUrl":"https://jobsearcher.com/jobs/b7fd41f8767eb8402a097b0d","title":"Program Manager","description":"DeepSight Technology is a rapidly growing ultrasound company dedicated to revolutionizing medical ultrasound imaging and interventional procedures. Using proprietary sensor technology and advanced Al, our platform (including the FDA-cleared NeedleVueTM LCI Ultrasound System) delivers real-time, high-precision guidance to redefine clinical standards and patient outcomes.\nPosition Summary\nWe are seeking a highly experienced and results-oriented Program Manager to lead the complex, cross-functional programs required to bring DeepSight's next-generation ultrasound systems and software features from development to commercial launch. The ideal candidate will have experience managing product development programs within the medical device industry.\nResponsibilities\nDrive complex product programs from initial concept/definition through commercial launch, ensuring successful product delivery and maximum team efficiency.\nProactively identify and mitigate program risks, working with technical experts to reconcile system performance and image artifacts to achieve the highest possible quality imaging solution.\nImplement Agile methodologies and performance management tools to provide accurate, transparent reporting and analytics of program outcomes, specifically leading integration teams focused on complex hardware-software integration.\nEstablish robust program governance and communication channels to proactively manage stakeholder expectations and secure high-quality, onschedule delivery across all product milestones.\nLead the strategic scoping and financial estimation for all new product initiatives and significant follow-on feature sets, translating technical complexity into clear business proposals.\nOversee and support the planning and execution of clinical evaluations necessary for product validation and regulatory submission.\nDirect and align the efforts of a multi-disciplinary team, including Engineering (Hardware, Software, Ultrasound Imaging, Instruments, Al), Clinical, Regulatory, and Manufacturing partners.\nAct as a driver for all FDA 51 0(k) and international regulatory submissions, ensuring all activities adhere to ISO 13485 Design Controls and are fully documented in the Design History File (DHF).\nRequired Qualifications\n8+ years of industry experience in Program Management, specifically bringing regulated medical device products to market.\nMaster of Science (M.S.) degree in Mechanical, Electrical, or Biomedical Engineering, or a related technical field.\nExpert knowledge of medical device Quality Management Systems (QMS), including deep proficiency in FDA standards, ISO 13485, and 510(k) submission processes.\nDemonstrated mastery of project management methodologies, with a proven ability to define the critical path and manage projects using project management tools.\nExceptional leadership skills in directing engineering teams, balancing competing priorities in a matrixed organization, and collaborating effectively with subject matter experts.\nStrong experience managing complex hardware and software integration programs, including balancing internal and external (contract manufacturing) resources.\nExcellent oral and written communication skills, with a track record of adapting quickly to change in a fast-paced environment.\nWillingness to travel up to 20%.\nPreferred Qualifications\nDirect experience leading product development teams in ultrasound imaging or equivalent medical device technology.\nPrior experience with devices designed for Interventional Procedures.\nExperience in a start-up or rapidly scaling environment.","company":"Deepsighttechnology","rawCompany":"deepsighttechnology","city":"St Louis","state":"MO","isRemote":false,"isActive":false,"createdAt":"2026-04-14T10:51:33.452Z","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":"11-9111.00","title":"Medical and Health Services Managers","slug":"medical-and-health-services-managers"}],"industries":[{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Program Manager","description":"DeepSight Technology is a rapidly growing ultrasound company dedicated to revolutionizing medical ultrasound imaging and interventional procedures. Using proprietary sensor technology and advanced Al, our platform (including the FDA-cleared NeedleVueTM LCI Ultrasound System) delivers real-time, high-precision guidance to redefine clinical standards and patient outcomes.\nPosition Summary\nWe are seeking a highly experienced and results-oriented Program Manager to lead the complex, cross-functional programs required to bring DeepSight's next-generation ultrasound systems and software features from development to commercial launch. The ideal candidate will have experience managing product development programs within the medical device industry.\nResponsibilities\nDrive complex product programs from initial concept/definition through commercial launch, ensuring successful product delivery and maximum team efficiency.\nProactively identify and mitigate program risks, working with technical experts to reconcile system performance and image artifacts to achieve the highest possible quality imaging solution.\nImplement Agile methodologies and performance management tools to provide accurate, transparent reporting and analytics of program outcomes, specifically leading integration teams focused on complex hardware-software integration.\nEstablish robust program governance and communication channels to proactively manage stakeholder expectations and secure high-quality, onschedule delivery across all product milestones.\nLead the strategic scoping and financial estimation for all new product initiatives and significant follow-on feature sets, translating technical complexity into clear business proposals.\nOversee and support the planning and execution of clinical evaluations necessary for product validation and regulatory submission.\nDirect and align the efforts of a multi-disciplinary team, including Engineering (Hardware, Software, Ultrasound Imaging, Instruments, Al), Clinical, Regulatory, and Manufacturing partners.\nAct as a driver for all FDA 51 0(k) and international regulatory submissions, ensuring all activities adhere to ISO 13485 Design Controls and are fully documented in the Design History File (DHF).\nRequired Qualifications\n8+ years of industry experience in Program Management, specifically bringing regulated medical device products to market.\nMaster of Science (M.S.) degree in Mechanical, Electrical, or Biomedical Engineering, or a related technical field.\nExpert knowledge of medical device Quality Management Systems (QMS), including deep proficiency in FDA standards, ISO 13485, and 510(k) submission processes.\nDemonstrated mastery of project management methodologies, with a proven ability to define the critical path and manage projects using project management tools.\nExceptional leadership skills in directing engineering teams, balancing competing priorities in a matrixed organization, and collaborating effectively with subject matter experts.\nStrong experience managing complex hardware and software integration programs, including balancing internal and external (contract manufacturing) resources.\nExcellent oral and written communication skills, with a track record of adapting quickly to change in a fast-paced environment.\nWillingness to travel up to 20%.\nPreferred Qualifications\nDirect experience leading product development teams in ultrasound imaging or equivalent medical device technology.\nPrior experience with devices designed for Interventional Procedures.\nExperience in a start-up or rapidly scaling environment.","datePosted":"2026-04-14T10:51:33.452Z","dateModified":"2026-04-14T10:51:33.452Z","hiringOrganization":{"@type":"Organization","name":"Deepsighttechnology","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"St Louis","addressRegion":"MO","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"b7fd41f8767eb8402a097b0d"},"url":"https://jobsearcher.com/jobs/b7fd41f8767eb8402a097b0d"}}