Job Board
LogoLogo

Get Jobs Tailored to Your Resume

Filtr uses AI to scan 1000+ jobs and finds postings that perfectly matches your resume

Johnson & Johnson Logo

Senior R&D Software Engineer - Shockwave Medical

Johnson & Johnson

$103,000 - $189,000
Sep 20, 2025
Santa Clara, CA, USA
Apply Now

Johnson & Johnson is looking to develop the next generation of smarter, less invasive, and more personalized treatments for complex calcified cardiovascular disease through Intravascular Lithotripsy (IVL). The Sr. R&D Software Engineer will contribute to the development of embedded software for innovative electronic medical devices.

Requirements

  • Demonstrated Proficiency in C language programming, C++ is a plus/desirable.
  • Experience with discrete microprocessors and/or Medical Grade Single Board Computers.
  • Proficient in the use of software development tools including compilers, assemblers, emulators, and in-circuit debugging tools, Oscilloscopes and Logic Analyzers.
  • Develop firmware for embedded system in Bare Metal, RTOS and Linux environment.
  • Proficient in the use of issue tracking tools such as JIRA.
  • Proficient in the use of source control repository systems such as GIT.
  • Experience with Configuration Management, Automated Testing and Software V&V.

Responsibilities

  • Design and develop software for medical device product(s) in full compliance with the company’s Design Control requirements and consistent with FDA, ISO, and MDD requirements.
  • Design and development of RTOS embedded software for use in medical devices.
  • Development of technical specifications from Product Level requirements.
  • Development, execution, and documentation of test plans.
  • Development, execution and functional verification to medical device standards.
  • Initiate and conduct design reviews.
  • Work with engineers in the development of design concepts.

Other

  • Participate on cross-functional development teams that manage projects from concept through commercialization.
  • Responsible for knowing and planning activities consistent with the company’s quality policy and quality objectives.
  • Responsible for ensuring lab notebooks are documented in a timely manner and consistent with the applicable SOP.
  • Support of medical device company audit processes.
  • Other duties as assigned.