Principal R&D Software Engineer - Shockwave Medical

Requirements

• Bachelor's Degree in Software/Electrical Engineering with 10+ years' design and development experience, or a Master's Degree with 8+ years.
• Experience in generating technical Requirement & design specifications required for Class III medical device products.
• Extensive experience in architecting and developing Software Systems using embedded proc

Benefits

Additional Information

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 jnj.com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: R&D Product Development Job Sub Function: R&D Software/Systems Engineering Job Category: Scientific/Technology All Job Posting Locations: Santa Clara, California, United States of America Job Description: Johnson & Johnson is hiring for a Principal R&D Software Engineer - Shockwave Medical to join our 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/ . 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. An internal pre-identified candidate for consideration has been identified. However, all applications will be considered. Position Overview The Principal R&D Software Engineer will lead technical development of innovative electronic systems to treat peripheral and heart valve diseases, will participate on multiple cross-functional development teams that manage projects from concept through commercialization, and will perform and support a variety of development and engineering activities with primary focus on analog high-voltage circuit design and development. Essential Job Functions - Lead the software development for medical device product(s) in full compliance with the company's Design Control requirements and consistent with FDA, ISO, and MDR requirements. - Define architecture of software system for next generation product including the development of RTOS/Bare Metal code on embedded processor(s). - Proficiency in writing code in C/C++ programming languages and understanding assembly language. - Develop User Interface applications operating system. - Develop code per IEC/EN 62304 medical device standard. - Understanding of communications protocols and developing driver for 1 Wire, I2C, SMBUS, SPI (QSPI), UART, and USB communication. - Proficient in the use of software development tools including compilers, assemblers, emulators, in-circuit debugging tools (IAR, REAL ICE, GDB etc), Oscilloscopes and Logic Analyzers. - Generate Software Requirement & Design specifications type documents from Product Specifications by decomposing into testable requirements. - Actively participate in Hazard Analysis, Design FMEA, Firmware Risk Assessment, Risk Control measure in a cross functional team setting. - Take ownership on development of DV protocols, provide test cases and test coverage for functional testing. Unit testing Integration testing. - Initiate and conduct software system code reviews. - Develop documentation per regulatory body guidelines. - Interface with internal regulatory affairs and assist with submissions. - Support of medical device company audits processes. - Understanding of electrical systems and reading schematics. - Debug/Troubleshoot complex systems and implement fixes. - Collaborate with HW Engineers to develop and implement design concepts. - Other duties as assigned.

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