Nevro Corp.

  • Principal Manufacturing Engineer

    Job Locations US-CA-Redwood City
    Job Post Information* : Posted Date 3 weeks ago(4/5/2018 7:02 PM)
    ID
    2018-2145
    Category
    Operations
  • About Nevro

    Nevro (NYSE: NVRO) is a public multinational medical technology company headquartered in Redwood City, California. We have developed HF10™ therapy, an innovative, evidence-based neuromodulation platform.

     

    We started with a simple mission to help more patients suffering from chronic pain. At each stage of development, our research was subject to the highest levels of scientific rigor, resulting in a new therapy that has impacted the lives of over 28,000 patients around the world.

     

    The Nevro® Senza® SCS System received CE mark in 2010, TGA approval in 2011, FDA approval in 2015, and is commercially available in Europe, Australia, and the United States.

    Overview

    This position plays a key role in supporting the manufacturing of a Class III implantable Neuromodulation system for pain management. This position reports to the Senior Director of Operations.

    Role Requirements

    • Supporting the manufacturing of Class III implantable Neuromodulation system components.
    • Defining manufacturing processes and executing manufacturing activities including qualification and validation.
    • Write, review and oversee verification and validation activities.
    • Resolving technical issues encountered during manufacturing. 
    • Providing troubleshooting training to contract manufacturing engineers and technicians.
    • Driving process improvements affecting yields, capacity increases, cycle time reductions and cost reduction initiatives.
    • Oversee technology and process transfers.
    • Participate in developing Process and Design FMEAs
    • Initiate and review ECOs.
    • Interfacing with other departments such as R&D, Regulatory, and Quality.
    • Working in accordance with Quality System procedures and actively enforces its objectives.

    Skills and Knowledge

    • B.S. Mechanical/Electrical Engineering, or similar degree. Advanced degree (M.S.) is preferred
    • A minimum of 10 years of experience within the Medical Device industry, preferably manufacturing and/or designing Active Implantable Medical Devices (AIMDs). 
    • Strong electro-mechanical design/manufacturing and analysis skills.
    • Experience with Solidworks a plus.
    • Good analytical and problem solving skills.
    • Functional familiarity with the FDA Submission process, ISO Requirements and QSR requirements is also preferred.
    • Strong interpersonal and technical writing skills.
    • Experience managing contract manufacturers. 
    • Knowledge and experience using structured project management tools.
    • Requires the ability to travel approximately 20% of the time throughout the United States and internationally.

    #LI-GR1

     

    .

    Nevro offers equal employment opportunity, regardless of race, color, creed, religion, national origin, marital or family status, sex, sexual orientation, gender expression (including religious dress and grooming practices), gender (including pregnancy, childbirth or medical condition related to pregnancy or childbirth), physical or mental condition, protected veteran status, disability, age or other characteristics protected by laws.

    Options

    Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
    Share on your newsfeed

    Connect With Us!

    Not ready to apply? Connect with us for general consideration.