Senior R&d Program Manager

Johnson & Johnson Johnson & Johnson · Pharma · Boston, MA +1

This role is for a Senior R&D Program Manager focused on the Navigation software portfolio within Digital R&D for Orthopaedics at Johnson & Johnson. The role involves platform-level program leadership, integrating strategy, priorities, software roadmap, and execution across multiple projects and workstreams in a regulated medical device environment. It requires leading governance, operating cadence, integrated program plans, and ensuring readiness for design reviews and software releases. The role emphasizes cross-functional collaboration with software, systems, cybersecurity, V&V, clinical, quality, and regulatory teams.

What you'd actually do

  1. Lead the Navigation software platform program, integrating strategy, priorities, software roadmap, and execution across multiple projects and workstreams.
  2. Own platform-level governance, including prioritization, sequencing, escalation pathways, and decision forums that span the Navigation software portfolio.
  3. Establish and drive the platform operating cadence, including PI planning, release planning, quarterly reviews, executive program reviews, and cross-functional governance routines.
  4. Own integrated program plans, milestones, release objectives, critical path, and interdependencies across projects to ensure execution remains aligned to strategic objectives and delivery commitments.
  5. Partner with Project Managers and technical leads to ensure project-level plans, RAID items, and change impacts are integrated into a platform-level view for leadership decision-making.

Skills

Required

  • Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related field
  • 10+ years of increasing responsibility in program or project leadership within regulated product development environments
  • Demonstrated experience leading multi-project programs, portfolios, or platform-level delivery models across complex cross-functional organizations
  • Experience leading complex programs through phase-gate execution, software release governance, design controls, and cross-functional decision processes
  • Strong technical background in medical device software development and/or surgical navigation systems, with the ability to engage credibly across software, systems, cybersecurity, and clinical domains
  • Strong command of regulated medical device development, including phase-gate execution, software lifecycle controls, design controls, and quality system requirements such as FDA 21 CFR 820.30 and I

Nice to have

  • advanced degree
  • Experience with Class II or III medical devices, navigation, robotics, or software-enabled systems

What the JD emphasized

  • regulated medical device environment
  • Class II or III medical devices
  • navigation, robotics, or software-enabled systems
  • phase-gate execution
  • software release governance
  • design controls
  • FDA 21 CFR 820.30