Principal R&D Project Manager - Shockwave at Johnson Johnson
Santa Clara, California, USA -
Full Time


Start Date

Immediate

Expiry Date

11 Oct, 25

Salary

169050.0

Posted On

11 Jul, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Qsr, Consideration, Interpersonal Skills, Iso, Communication Skills

Industry

Information Technology/IT

Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

JOB DESCRIPTION:

Johnson & Johnson is hiring for a Principal R&D Project Manager – Shockwave to join our team located in Santa Clara, CA.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease. Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.

POSITION OVERVIEW

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. Responsible for gaining cross functional alignment on strategic vision and goals of projects, meeting project goals and ensuring that appropriate resources are identified and allocated. The role supports R&D New Product Development and/or On Market.

REQUIREMENTS

  • BS/BA in science, engineering or business administration or equivalent combination of education and work experience.
  • 10+ years of Medical Device experience including least 5 years of project management experience in the medical device industry.
  • Experience in Quality System Regulations (QSR) 21 CFR 820, ISO 13485, MDR requirements, and other applicable regulations as required.
  • Project Management specific training and/or certification is highly preferred.
  • Experience with developing, implementing, and monitoring process improvement initiatives, project management frameworks and methodologies.
  • Highly capable performing under the pressure of multiple competing deadlines while maintaining a cooperative and constructive working relationship with others.
  • Excellent leadership and interpersonal skills, adept at navigating organizational challenges and possess ability to work through others and accomplish objectives.
  • Outstanding verbal & written communication skills.
  • High level of enthusiasm, motivation, and drive for results.
  • Proven ability to navigate ambiguity.
    NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as assigned or negotiated to meet the ongoing needs of the organization.
    Equal Opportunity Employer
    An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.
Responsibilities

Please refer the Job description for details

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