Principal R&d Project Manager - Shockwave Medical

Johnson & Johnson MedTech

Santa Clara, California, United States
Base: $125,000.00 - $201,250.00; bonus/equity: eli...
Not specified (assumed to be hybrid based on industry norms).
Project planning and risk management
Cross-functional team coordination
Design control compliance
Johnson & Johnson MedTech is seeking a Principal R&D Project Manager for its Shockwave Medical team in Santa Clara, California. The role focuses on managing product development and project activities, aiming to innovate and commercialize medical device solutions for cardiovascular diseases

Job Summary

  • Johnson & Johnson is pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
  • The Principal R&D Project Manager is responsible for managing all phases of product development, resource allocation, and cross-functional alignment to meet project goals.
  • Employees are eligible for comprehensive benefits including retirement plans, long-term incentives, various paid time off options, and inclusive interview accommodations.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Principal R&D Project Manager for its Shockwave Medical team in Santa Clara, California. The role focuses on managing product development and project activities, aiming to innovate and commercialize medical device solutions for cardiovascular diseases.

Salary

Base: $125,000.00 - $201,250.00; Bonus/Equity: Eligible for long-term incentive program; Benefits: Retirement plans, paid time off, parental leave, and more

Skills & Requirements

Must-have

  • Project planning and risk management
  • Cross-functional team coordination
  • Design Control compliance
  • Medical device product development
  • Regulatory quality system knowledge
  • Project execution and communication

Nice-to-have

  • Mentoring project managers
  • Process improvement initiatives
  • Effective presentation skills
  • Leadership and interpersonal skills
  • Navigating organizational challenges
  • High motivation and drive

Key Requirements

  • BS/BA in science, engineering or business
  • 10+ years medical device experience
  • 5+ years project management experience
  • Knowledge of QSR 21 CFR 820 and ISO 13485
  • Experience with MDR requirements
  • Project management certification preferred

Work Rights

Not specified

Tailored Resume

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