FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.

Vice President – Software Engineering
iRhythm Technologies, Inc.. Lead end-to-end software engineering execution across clinical, patient-facing, platform, and device-integrated software systems in a regulated Software as a Medical Device environment .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading software engineering execution in regulated environments, particularly in Software as a Medical Device (SaMD), while ensuring compliance with FDA regulations and quality standards. Proven ability to mentor leaders, drive organizational change, and foster a metrics-driven engineering culture.
Highest-signal resume keywords
Software as a Medical Device (SaMD)FDA Software RegulationsCI/CD FrameworksLeadership in Engineering OrganizationsRegulatory Compliance in Software Development
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Software Development LifecycleEngineering Operating SystemsAutomation ToolsMetrics-Driven EngineeringTechnical AssessmentsQuality Management Systems (QMS)AI-Assisted Software DevelopmentSoftware ArchitectureVerification and ValidationRegulatory Approval Processes
Soft Skills
Cross-Functional CollaborationExecutive Stakeholder InfluenceMentoring and Leadership DevelopmentStrategic LeadershipChange Management
Tools & Technologies
Engineering Enablement ToolsCloud PlatformsData EcosystemsConnected ProductsDigital Health Technologies
Certifications & Qualifications
Bachelor's Degree in Computer ScienceAdvanced Degree Preferred
Industry Keywords
HealthcareMedical DeviceDigital HealthRegulated TechnologySoftware Quality Standards
Tech Stack
Tools & technologiesCloudCyber Security
About the role
Key responsibilities & impact- Lead end-to-end software engineering execution across clinical, patient-facing, platform, and device-integrated software systems in a regulated Software as a Medical Device environment
- Establish and evolve engineering operating systems, governance frameworks, and development practices
- Improve engineering velocity, product quality, release confidence, system reliability, and customer outcomes
- Ensure software development lifecycle processes meet FDA, IEC 62304, ISO 13485, cybersecurity, and internal QMS requirements
- Translate technical concepts, delivery risks, and strategic tradeoffs for executive leadership and stakeholders
- Advance CI/CD frameworks, development platforms, automation, and engineering enablement tools
- Govern AI-assisted software development practices
- Establish a metrics-driven engineering culture using operational and quality indicators
- Build, lead, and develop software engineering directors, managers, and senior technical leaders
- Mentor engineering leaders and cultivate leadership capability, organizational resilience, continuous improvement, innovation, and technical excellence
- Partner with Product Security, Software Quality, Research & Systems Engineering, Machine Learning, and IT
- Align Product Management, Clinical, Quality, Regulatory, and other cross-functional teams from concept through commercialization
- Lead software engineering diligence, technical assessments, and post-acquisition integration activities
- Contribute to long-term software platform, architecture, and technology strategy
Requirements
What you’ll need- Bachelor's degree in Computer Science, Engineering, or a related technical discipline required
- 10+ years of progressive software engineering leadership experience
- Experience leading large-scale engineering organizations and senior technology leaders
- Success leading development and delivery of Software as a Medical Device (SaMD) solutions in highly regulated medical device environments
- Experience taking regulated software products from concept through development, verification, validation, regulatory approval, commercialization, and post-market support
- Deep expertise in FDA software regulations, IEC 62304, ISO 13485, and medical device quality systems
- Experience applying regulatory requirements within modern software development environments
- Experience leading complex, matrixed software engineering organizations through growth, transformation, organizational change, and technology modernization
- Advanced degree preferred
- Experience in healthcare, medical device, digital health, or regulated technology organizations preferred
- Experience scaling organizations supporting connected products, cloud platforms, data ecosystems, and customer-facing applications preferred
- Exposure to technical diligence, integration planning, or software leadership support for mergers and acquisitions preferred
- Experience modernizing software delivery capabilities, including CI/CD, automation, and engineering productivity tools within regulated environments preferred
- Experience evaluating, implementing, and governing AI-assisted software development practices preferred
- Strategic and execution-oriented leadership
- Ability to translate business priorities into operational excellence and measurable outcomes
- Experience developing leaders and building high-performing teams
- Exceptional cross-functional collaboration and executive stakeholder influence
- Data-driven, pragmatic, and decisive approach
- Ability to lead through complex change, growth, and transformation
Benefits
Comp & perks- Reasonable accommodations for qualified individuals with disabilities in job application procedures
- Inclusive workforce and equal opportunity employment