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iRhythm Technologies, Inc.

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 .

Posted 10/7/2026full-timeRemote • United StatesLead💰 $278,000 - $361,000 per yearWebsite

Core Competencies

Role fit
Core 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

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Applicant Tracking System Keywords

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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 & technologies
CloudCyber 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