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Johnson & Johnson is seeking a Principal R&D Project Manager for Shockwave Medical in Santa Clara, CA, to oversee product development and project management activities related to innovative medical solutions. The ideal candidate will have extensive experience in the medical device industry, strong project management skills, and a commitment to health innovation.
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Job Summary
The Principal R&D Project Manager is responsible for product development, resource, and project management activities associated with executing the company's goals for product commercialization.
The role supports R&D New Product Development and/or On Market, overseeing all phases of the product development process from Feasibility to Market Release.
Johnson & Johnson is committed to providing an inclusive work environment where each person is considered as an individual and their diversity and dignity are respected.
Matching Summary
Match Score: 75
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Johnson & Johnson is seeking a Principal R&D Project Manager for Shockwave Medical in Santa Clara, CA, to oversee product development and project management activities related to innovative medical solutions. The ideal candidate will have extensive experience in the medical device industry, strong project management skills, and a commitment to health innovation.
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Salary
Base: $125,000.00 - $201,250.00; Bonus/Equity: Eligible for long-term incentive program; Benefits: Vacation, Sick time, Holiday pay, Work/Personal/Family Time, Parental Leave, Bereavement Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off
Skills & Requirements
Must-have
Manage cross-functional activities
Product development lifecycle
Design Control requirements
Project planning and risk management
Develop routine dashboards and reports
Lead complex new product development projects
Nice-to-have
Pioneering development of Intravascular Lithotripsy
Treating complex calcified cardiovascular disease
Establish new standard of care
Innovate across healthcare solutions
Inclusive work environment
Key Requirements
10+ years Medical Device experience
5+ years project management experience
Experience with QSR 21 CFR 820, ISO 13485, MDR
BS/BA in science, engineering or business administration
Project Management specific training/certification preferred