Project Head, New Product Development - Medtech

Johnson & Johnson Johnson & Johnson · Pharma · Cincinnati, OH +1

Project Head for New Product Development in MedTech at Johnson & Johnson, focusing on end-to-end execution of NPD programs, cross-functional collaboration, and delivery of surgical technologies. Requires strong technical expertise in medical device development and understanding of global regulatory and clinical requirements.

What you'd actually do

  1. Accountable for end‑to‑end execution and delivery of their New Product Development (NPD) program, including scope, schedule, and cost.
  2. Owns Communication of the program status, including program planning, tracking, and risk management, proactively identifying issues, driving mitigation plans, and accelerating progress to meet business objectives.
  3. Leads cross‑functional program execution as the single point of accountability, partnering effectively with R&D, Supply Chain, Quality, Regulatory, Clinical, Finance, and Marketing.
  4. Establishes and maintains disciplined operating rhythms, including core team meetings and milestone planning, that promote clarity, accountability, and efficient execution.
  5. Manages the program triple constraint (time, scope, resources) by securing trade‑off decisions, escalating risks appropriately, and resolving cross‑functional challenges.

Skills

Required

  • Bachelors degree in an engineering or scientific discipline
  • 8+ years of New Product Development work experience
  • 3 years working in a regulated industry experience
  • results and performance driven demeanor with strong sense of accountability
  • Demonstrated success leading regulated programs through market introduction
  • Proven ability to lead and influence across a complex, matrixed organization
  • Strong capability in strategic planning, execution, and operational excellence
  • Demonstrated effectiveness in change leadership and navigating ambiguity
  • Up to 20% Domestic and International travel

Nice to have

  • advanced degree
  • medical device development, including Class II and/or Class III products
  • leading R&D teams, including direct or indirect people leadership
  • Strong understanding of global regulatory and clinical requirements for medical devices
  • technical depth and business acumen supporting strategic decision‑making and execution
  • ability to develop talent, build inclusive team cultures, and drive sustained performance

What the JD emphasized

  • New Product Development work experience is required
  • working in a regulated industry experience is required
  • results and performance driven demeanor with strong sense of accountability is required
  • Demonstrated success leading regulated programs through market introduction is required
  • Proven ability to lead and influence across a complex, matrixed organization is required
  • Strong capability in strategic planning, execution, and operational excellence is required
  • Demonstrated effectiveness in change leadership and navigating ambiguity is required
  • Domestic and International travel required