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R&D Engineer II (Process Development) – Shockwave Medical

Johnson & Johnson
Santa Clara, CA Other
POSTED ON 2/11/2025 CLOSED ON 2/19/2025

What are the responsibilities and job description for the R&D Engineer II (Process Development) – Shockwave Medical position at Johnson & Johnson?

Johnson & Johnson is hiring for a R&D Engineer II (Process Development) – Shockwave Medical to join our R&D team located in Santa Clara, CA.

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/.

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges. We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

Shockwave Medical, Inc., recently acquired by Johnson & Johnson, is a pioneer in the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease. Shockwave Medical 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 R&D Engineer II will use technical skills in the development of innovative products to treat peripheral, coronary, and heart valve diseases. The R&D Engineer II will focus on process development for the engineering team, providing oversight to pilot manufacturing/testing, and see products transition from development into full production. This position will participate on multiple cross-functional development teams that focus on process optimization, sustaining, and design support. The R&D Engineer II will develop, validate, and implement various processes by working closely with research/development, operations, regulatory, and quality teams.

Essential Job Functions

  • Support the development of product(s) for manufacturing in full compliance with the company’s Design Control requirements and consistent with FDA, ISO, and MDR requirements
  • Work on prototype and develop designs, processes, and test methods in support of new product designs scaling for commercialization
  • Represent R&D on manufacturing-related project activities, including internal and external requests.
  • Analyzes, evaluates, sources, and coordinates the procurement of new materials to support prototyping and pilot operation
  • Participate on cross-functional development team that manage projects from concept through commercialization
  • Responsible for ensuring proper documentation consistent with company’s quality system
  • Responsible for knowing and planning activities consistent the company’s quality policy and quality objectives
  • Responsible for ensuring the lab notebooks are documented in a timely manner and consistent with the applicable SOP
  • Write protocols/reports and perform product verification and validation testing
  • Perform process-related design tasks to support pilot manufacturing
  • Identify suppliers and maintain relationships to ensure the delivery of superior components and services
  • Responsible for component and assembly documentation for new products being developed
  • Support company goals and objectives, policies and procedures, Quality Systems, and FDA regulations
  • Other duties as assigned
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