Principal R&d Project Manager

Johnson & Johnson Johnson & Johnson · Pharma · Gières, Isere, France

The Principal R&D Project Manager will plan and execute projects within the Navigation platform in Digital R&D, ensuring delivery against scope, schedule, cost, and quality in a regulated medical device environment. This role involves managing cross-functional teams, project budgets, risks, and design controls to achieve predictable delivery outcomes.

What you'd actually do

  1. Own project planning and baseline management for assigned Navigation projects, including project charter, scope baseline, WBS, and an integrated master schedule aligned to the platform program plan.
  2. Manage project schedule execution, critical path tracking, milestone readiness, and schedule recovery actions; maintain and communicate weekly status to the platform leadership team.
  3. Own the project budget baseline, track actuals and forecasts, and perform earned value management (EVM) tracking; provide inputs for program-level financial reviews and funding decisions.
  4. Maintain the project RAID log (risks, issues, assumptions, dependencies) with proactive mitigation actions; escalate cross-project or platform-level risks and decisions through the Platform Program Manager.
  5. Lead weekly project core team meetings, drive action/decision tracking, and ensure timely follow-through across cross-functional contributors.

Skills

Required

  • Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related field.
  • 5+ years of project management experience within regulated class II and product development environments (medical device, robotics, navigation, or software-enabled products preferred).
  • Experience with phase-gate execution and design controls documentation in a QMS environment.
  • Deep understanding of regulated medical device product development and phase-gate execution, including FDA 21 CFR 820.30 / ISO 13485 design controls.
  • Experience managing complex, cross-functional programs across software, systems, and hardware, including integrated planning across requirements, architecture, V&V, clinical, quality, and regulatory deliverables.

What the JD emphasized

  • regulated medical device environment
  • design controls
  • phase-gate execution