Senior Manager, R&d Software Engineering

Johnson & Johnson Johnson & Johnson · Pharma · Milpitas, CA +1

Senior Manager, R&D Software Engineering for a medical device Vision team, leading a team in the development of safety-critical medical device applications and embedded software systems. Responsibilities include guiding architecture, design, development, integration, and ensuring compliance with regulatory standards like FDA 21 CFR Part 820 and IEC 62304. The role involves project management, talent development, and hands-on troubleshooting.

What you'd actually do

  1. Lead and mentor a team of software engineers.
  2. Define team goals, development roadmaps, and performance metrics.
  3. Guide architecture, design, development, and integration for safety critical medical device application and embedded software systems using (but not limited to) C/C++, Python, Qt, LabVIEW, .NET.
  4. Ensuring all software development complies with regulatory standards (e.g., FDA 21 CFR Part 820, IEC 62304).
  5. Manage multiple concurrent projects, balancing priorities and resources.

Skills

Required

  • Software engineering leadership
  • Agile methodologies
  • Medical device software development
  • C/C++
  • Python
  • Qt
  • LabVIEW
  • .NET
  • Embedded systems
  • Hardware integration
  • Version control
  • CI/CD
  • Unit Testing
  • Debugging
  • Cybersecurity
  • Privacy
  • Project management
  • Cross-functional collaboration
  • Talent development
  • Performance reviews
  • Career development planning

Nice to have

  • SPI
  • I2C
  • UART
  • USB

What the JD emphasized

  • safety critical medical device application
  • FDA 21 CFR Part 820
  • IEC 62304
  • regulatory standards