Electrical Engineer

Job Locations US-CA-Redwood City
Job Post Information* : Posted Date 2 weeks ago(11/14/2022 11:41 PM)
ID
2022-3867
Category
Research & Development

About Nevro

Nevro (NYSE: NVRO) is a global medical device company headquartered in Redwood City, California. The company is focused on delivering comprehensive, life-changing solutions that continue to set the standard for enduring patient outcomes in chronic pain treatment.

 

We started with a simple mission to help more patients suffering from debilitating pain and developed our proprietary 10 kHz Therapy, an evidence-based, non-pharmacologic innovation that has impacted the lives of more than 80,000 patients globally.

 

Nevro’s comprehensive HFX™ spinal cord stimulation (SCS) platform includes a Senza SCS system and support services for the treatment of chronic trunk and limb pain and painful diabetic neuropathy. Senza®, Senza II®, and Senza Omnia™ are the only SCS systems that deliver Nevro's proprietary 10 kHz Therapy. Nevro’s unique support services provide every patient with an HFX Coach™ throughout their pain relief journey and every physician with HFX Cloud™ insights for enhanced patient and practice management.

Job Summary & Responsibilities

You will be key in development of Nevro’s next generation Class III systems and accessories. Your passion is twofold:  working in cutting-edge medical technology while significantly impacting lives. You are precise, obsessed about quality, and driven to make a difference with your EE talents.

 

  • Develop the next generation of implantable neuromodulation systems and other accessories
    (remotes, chargers, etc.).
  • Design Electronic Circuits (Embedded Systems, Mixed Analog/Digital Circuits, Power Regulators, etc.)
  • Responsible for Schematics Design and PCB Layout.
  • Investigate and determine root cause of system failures.
  • Advise the development of firmware for corresponding hardware.
  • Design experiments to characterize hardware, devise test plans, interpret data and present reports.
  • Contribute to the leadership and organization of work for a small team/project.
  • Responsible for planning, developing, coordinating, and directing their own work, collaborating with other internal and external resources to be successful.
  • Operates at the capacity of an expert in the field.
  • Interface with external stakeholders as the primary point of contact and/or technical expert for one or more product areas.
  • Proactively identify areas of developmental risk and communicate these to management
  • Foster an environment of proactive cooperation and open communication.
  • Guide contributions into final manufactured products.
  • Assure contributions interface properly with all aspects of the system.
  • Meet or exceed performance requirements by working closely with other product development team members.
  • Contribute to the intellectual property base of the company via active communication of new concepts to management.
  • Work in accordance with quality system procedures and actively enforce its objectives.

Role Requirements

  • B.S. in Electrical Engineering or Computer Engineering or Biomedical Engineering (and/or similar degree) minimum.  
  • 3+ years related experience. Equivalent years of experience may be substituted for the education requirement.
  • Medical device or other regulated industry experience, such as aerospace or automotive desired, but not required.

Skills and Knowledge

  • Good analytical and problem-solving
  • Excellent oral and written communications, including good presentation and technical writing
  • Functional familiarity with the FDA Submission process, ISO Requirements and QSR requirements are preferred, but not required.
  • Requires the ability to travel approximately 10% of the time (domestic and international).

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