Senior Director, Software Development Practices Transformation

GE Healthcare GE Healthcare · Healthcare · Waukesha, WI +1 · Digital Technology / IT

This role focuses on transforming and scaling modern software development practices, particularly for SaMD and SiMD, within GE Healthcare's regulated medical software environment. The Senior Director will lead a cross-functional Steering Committee, partner with consultants, and establish enterprise-wide standards to improve quality and velocity in the digital New Product Introduction (NPI) process, ensuring speed with safety and regulatory compliance.

What you'd actually do

  1. Drive the evolution of software development practices as part of the IronMan acquisition, and beyond the Ironman pilot. Embed standardized processes, scalable capabilities, and modern tools across every GE HealthCare segment, ultimately improving quality and velocity across the company’s entire new‑product pipeline.
  2. Serve as the day-to-day leader for the software development Steering Committee, orchestrating priorities, decisions, and communications across engineering, quality, regulatory, product management, and commercial teams. Strengthens organizational alignment by delivering clear, timely communications that enable leaders to understand strategic direction and progress, while ensuring the wider organization is aware of key objectives and outcomes.
  3. Define and deploy a medtech-adapted DORA metric stack to measure software performance and flow, with targets that include critical security and quality patches released in under 10 days where applicable.
  4. Establish a process-agile PRD approach that supports iterative learning cycles, clear scope control, and traceability to user and clinical needs.
  5. Operationalize a process-agile QMS guided by AAMI TIR45 for SaMD and SiMD, aligning design controls and documentation with lean, risk-based software practices.

Skills

Required

  • Bachelor’s degree in Computer Science, Software Engineering, Electrical Engineering, Biomedical Engineering, or related field
  • 10+ years in software development for medical devices or regulated health software, including SaMD and SiMD experience
  • Demonstrated mastery of modern software development life cycles and DevSecOps, including CI/CD, automated testing, and release management in regulated contexts
  • Previous experience as a lead software integrator or architect on major GE HealthCare NPIs, with hands-on understanding of segment-specific architectures and constraints
  • People leadership experience managing software engineering teams and cross-functional program leadership across quality, regulatory, clinical, and product management
  • Proven ability to drive enterprise-scale change through standards, governance, and coaching, with measurable improvements in flow, quality, and reliability
  • Strong communication, influencing, and stakeholder management skills across executive, technical, and field audiences

Nice to have

  • advanced degree preferred
  • Thought leader who can scale initial Steering Committee and consultant progress into full enterprise implementation
  • Deep understanding of GE HealthCare segment software development environments, including platform reuse and integration patterns
  • Fluent in agile methods for regulated software, including risk-based documentation, incremental verification, and usability engineering integration
  • Strong business and financial acumen to prioritize investments and articulate ROI for tooling, automation, and platform strategies
  • Change management expert who builds durable habits through coaching, enablement, and communities of practice
  • Excellent written and verbal communicator with the ability to simplify complex concepts for diverse stakeholders

What the JD emphasized

  • regulated medical software
  • SaMD and SiMD
  • regulated contexts
  • regulatory compliance