Nevro Corp.

  • Quality Engineer I - Temp

    Job Locations US-CA-Redwood City
    Job Post Information* : Posted Date 2 months ago(11/22/2019 2:57 PM)
    ID
    2019-2758
    Category
    Quality
  • About Nevro

    Nevro (NYSE: NVRO) is a global medical device company headquartered in Redwood City, California. We are focused on providing innovative products that improve the quality of life of patients suffering from debilitating chronic pain.

     

    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 55,000 patients around the world.

     

    Nevro has developed and commercialized the Senza spinal cord stimulation (SCS) system, an evidence-based, non-pharmacologic neuromodulation platform for the treatment of chronic pain. HF10 therapy has demonstrated the ability to reduce or eliminate opioids in ≥65% of patients across six peer-reviewed clinical studies. The Senza® System, Senza II™ System, and the Senza® Omnia™ System are the only SCS systems that deliver Nevro's proprietary HF10® therapy.

    Job Summary & Responsibilities

    The Quality Engineer I is responsible for Quality Assurance activities related to the life cycle of the product. 

    • Travel to and manage manufacturing assembly process at Suppliers
    • Perform data analysis for root cause investigations
    • Understand and execute testing
    • Support
      • Product Verification & Validation activities
      • Design Control Documentation
      • CAPA /NCMR
      • Risk Management
      • External Standards and Regulatory Audits
      • Manufacturing Support
    • Perform other duties as required

    Role Requirements

    • Bachelor’s degree in a technical or science major. Master’s Degree preferred.
    • 0-2 years of Quality/Regulatory experience in a medical device or other regulated industry

    Skills and Knowledge

    • Able to understand ISO and FDA compliance standards
    • Able to understand failure analysis and troubleshooting
    • Attention to Detail
    • Interact with suppliers
    • Able to work well with others
    • Able to articulate and present findings to management
    • Able to adapt well to changing priorities and assignments
    • Perform tasks with limited supervision

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