{"schemaVersion":"jobsearcher.job.v1","id":"70945d2ea8709c82e984d9d8","url":"https://jobsearcher.com/jobs/70945d2ea8709c82e984d9d8","canonicalUrl":"https://jobsearcher.com/jobs/70945d2ea8709c82e984d9d8","title":"Software Project Lead","description":"Job Title: Software Project Lead (W2 only)\nJob Location: Valencia, CA 91355 (Hybrid - 3 days)\nJob Duration: 12+ months W2 contract (with high possibility of extension based on performance and depending on business needs)\nPay Range: $60 to $69.04/Hour on W2\nAbout the role:\nThis role serves as the primary owner for software activities, aligning technical execution with business objectives, regulatory expectations, and product roadmaps.\nAs a key member of the Software group and is critical to accelerating innovation through acquisition while maintaining patient safety, regulatory compliance, and software quality. The Software Project Lead ensures that acquired software technologies are seamlessly and responsibly integrated into the medical device portfolio—turning strategic investments into safe, effective products for patients.\nRequired Qualifications:\nBachelor’s degree in engineering, Computer Science, or related technical discipline.\n10-15 years of experience in software project management within software driven medical devices or other regulated industries.\nDemonstrated experience leading cross functional software development programs.\nStrong understanding of regulated software development lifecycles and quality systems.\nProven ability to manage complex, ambiguous programs with multiple stakeholders.\nAdditional Required Qualifications:\nSoftware Development and Engineering Manager experience is required.\nApproximately 5 years of hands-on experience developing software using C# and WPF (Windows Presentation Foundation) as a Software Developer and/or Software Engineering Manager.\nCandidates should have a strong technical background in software development in addition to program/project management experience.\nResponsibilities:\nLeading the planning and execution of complex software development and integration software.\nPartnering closely with R&D, Quality, Regulatory, IT, Cybersecurity, Clinical, Operations and other cross-functional teams to develop software solution into the company’s medical device portfolio while ensuring compliance with global regulatory standards and internal quality systems.\nDevelop and maintain plans covering software development, verification/validation, cybersecurity, and regulatory deliverables.\nManage program schedules, budgets, resources, risks, and interdependencies across multiple cross functional teams.\nProvide clear, data driven program status, risks, and decision points to R&D leadership.\nDrive alignment between legacy and acquired development processes, tools, architectures, and documentation.\nWork closely with software engineering teams to ensure development and integration activities comply with applicable standards.\nEnsure proper integration of software lifecycle artifacts, including requirements, architecture, risk management, verification, validation, and cybersecurity documentation.\nSupport design reviews, phase gate reviews, and regulatory submissions related to integrated software products.\nFacilitate alignment on system architectures, interfaces, data flows, and platform strategies across organizations.\nDrive issue resolution and decision making across organizational boundaries.\nTrack software project progress and provide transparent communication and interfaces with all areas affected by the project including cross-functional stakeholders, business sponsors, and senior management.\nConduct retrospectives, and lessons learned, and implement process improvement initiatives to drive future success.\nAdditional duties, as assigned.\nKey Competencies and Capabilities:\nAbility to plan and execute software projects in the medical device industry, with preferred experience in medical device software, including new product development and sustaining software.\nWorking knowledge of the software development lifecycle (SDLC) in a regulated environment, with exposure to agile or hybrid delivery models.\nProficiency with project management and software delivery tools (e.g., MS Project, JIRA), including development of WBS, schedules, and dependency tracking.\nWorking understanding of software day to day challenges and system level integration, sufficient to support cross functional execution.\nStrong verbal and written communication skills, with the ability to collaborate across Software, Systems, Quality, and Regulatory teams and drive on time delivery.\nDemonstrated organizational and problem-solving skills, with the ability to manage assigned Product and operate effectively within a regulated, quality driven environment.\nPreferred Qualifications:\nExperience developing Software for medical devices.\nFamiliarity with FDA, EU MDR, and global regulatory expectations for software enabled medical devices.\nExperience with cybersecurity, cloud connected devices.\nPMP, PgMP, Agile, or SAFe certification.\nMaster’s degree in engineering, Management, or related field.\n#IRI-IT\nPay: $60.00 - $69.04 per hour\nBenefits:\n401(k)\nDental insurance\nHealth insurance\nWork Location: Hybrid remote in Valencia, CA 91355","company":"Integrated Resources Hosted","rawCompany":"integrated resources hosted","city":"Valencia","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-08-08T13:21:51.403Z","occupations":[{"code":"15-1252.00","title":"Software Developers","slug":"software-developers"},{"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"}],"industries":[{"code":"541511","title":"Custom Computer Programming Services","slug":"custom-computer-programming-services"},{"code":"541512","title":"Computer Systems Design Services","slug":"computer-systems-design-services"},{"code":"513210","title":"Software Publishers","slug":"software-publishers"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Software Project Lead","description":"Job Title: Software Project Lead (W2 only)\nJob Location: Valencia, CA 91355 (Hybrid - 3 days)\nJob Duration: 12+ months W2 contract (with high possibility of extension based on performance and depending on business needs)\nPay Range: $60 to $69.04/Hour on W2\nAbout the role:\nThis role serves as the primary owner for software activities, aligning technical execution with business objectives, regulatory expectations, and product roadmaps.\nAs a key member of the Software group and is critical to accelerating innovation through acquisition while maintaining patient safety, regulatory compliance, and software quality. The Software Project Lead ensures that acquired software technologies are seamlessly and responsibly integrated into the medical device portfolio—turning strategic investments into safe, effective products for patients.\nRequired Qualifications:\nBachelor’s degree in engineering, Computer Science, or related technical discipline.\n10-15 years of experience in software project management within software driven medical devices or other regulated industries.\nDemonstrated experience leading cross functional software development programs.\nStrong understanding of regulated software development lifecycles and quality systems.\nProven ability to manage complex, ambiguous programs with multiple stakeholders.\nAdditional Required Qualifications:\nSoftware Development and Engineering Manager experience is required.\nApproximately 5 years of hands-on experience developing software using C# and WPF (Windows Presentation Foundation) as a Software Developer and/or Software Engineering Manager.\nCandidates should have a strong technical background in software development in addition to program/project management experience.\nResponsibilities:\nLeading the planning and execution of complex software development and integration software.\nPartnering closely with R&D, Quality, Regulatory, IT, Cybersecurity, Clinical, Operations and other cross-functional teams to develop software solution into the company’s medical device portfolio while ensuring compliance with global regulatory standards and internal quality systems.\nDevelop and maintain plans covering software development, verification/validation, cybersecurity, and regulatory deliverables.\nManage program schedules, budgets, resources, risks, and interdependencies across multiple cross functional teams.\nProvide clear, data driven program status, risks, and decision points to R&D leadership.\nDrive alignment between legacy and acquired development processes, tools, architectures, and documentation.\nWork closely with software engineering teams to ensure development and integration activities comply with applicable standards.\nEnsure proper integration of software lifecycle artifacts, including requirements, architecture, risk management, verification, validation, and cybersecurity documentation.\nSupport design reviews, phase gate reviews, and regulatory submissions related to integrated software products.\nFacilitate alignment on system architectures, interfaces, data flows, and platform strategies across organizations.\nDrive issue resolution and decision making across organizational boundaries.\nTrack software project progress and provide transparent communication and interfaces with all areas affected by the project including cross-functional stakeholders, business sponsors, and senior management.\nConduct retrospectives, and lessons learned, and implement process improvement initiatives to drive future success.\nAdditional duties, as assigned.\nKey Competencies and Capabilities:\nAbility to plan and execute software projects in the medical device industry, with preferred experience in medical device software, including new product development and sustaining software.\nWorking knowledge of the software development lifecycle (SDLC) in a regulated environment, with exposure to agile or hybrid delivery models.\nProficiency with project management and software delivery tools (e.g., MS Project, JIRA), including development of WBS, schedules, and dependency tracking.\nWorking understanding of software day to day challenges and system level integration, sufficient to support cross functional execution.\nStrong verbal and written communication skills, with the ability to collaborate across Software, Systems, Quality, and Regulatory teams and drive on time delivery.\nDemonstrated organizational and problem-solving skills, with the ability to manage assigned Product and operate effectively within a regulated, quality driven environment.\nPreferred Qualifications:\nExperience developing Software for medical devices.\nFamiliarity with FDA, EU MDR, and global regulatory expectations for software enabled medical devices.\nExperience with cybersecurity, cloud connected devices.\nPMP, PgMP, Agile, or SAFe certification.\nMaster’s degree in engineering, Management, or related field.\n#IRI-IT\nPay: $60.00 - $69.04 per hour\nBenefits:\n401(k)\nDental insurance\nHealth insurance\nWork Location: Hybrid remote in Valencia, CA 91355","datePosted":"2026-08-08T13:21:51.403Z","dateModified":"2026-08-08T13:21:51.403Z","hiringOrganization":{"@type":"Organization","name":"Integrated Resources Hosted","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Valencia","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"70945d2ea8709c82e984d9d8"},"url":"https://jobsearcher.com/jobs/70945d2ea8709c82e984d9d8"}}