Nevro Corp.

  • Sr. Manager Operations

    Job Locations US-CA-Redwood City
    Job Post Information* : Posted Date 3 weeks ago(3 weeks ago)
  • About Nevro

    Nevro is a medical device company headquartered in Redwood City, California. We have developed HF10™ therapy, an innovative, evidence-based neuromodulation platform for the treatment of 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 advanced the state of spinal cord stimulation (SCS).

    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.


    Nevro is seeking a Senior Manager of Operations that will play a key role in managing the manufacturing of a Class III implantable Neuromodulation system for pain management in a smooth, continuous, and cost effective manner. This position reports to the Senior Director of Operations.

    Role Requirements

    At a minimum a Mechanical or Electrical Engineering BS degree and 12 years of relevant experience, with at least 4+ years of experience in active implantable medical devices.

    Skills and Knowledge

    • S. Mechanical or Electrical Engineering. Advanced degree (M.S.) is preferred.
    • A minimum of 12 years of experience within the Medical Device industry, preferably manufacturing of Active Implantable Medical Devices (AIMDs).
    • Knowledge of the manufacturing processes of Implantable Pulse Generators (IPGs) and External devices is a plus.
    • Prior experience working and managing Contract Manufacturers.
    • Proven leadership skills and track record of mentoring people and advancing the organization.
    • Outstanding communication and presentation skills (written and verbal) to all levels of an organization.
    • Self-starting, self-motivated, self-directed, and self-sufficient.
    • Naturally accountable and responsible.
    • Exceptional attention to detail.
    • Knowledge and experience using structured project management tools.
    • Demonstrated creative and critical thinking capabilities.
    • Must possess a professional demeanor and demonstrated effectiveness working with others.
    • Demonstrated engineering management skills, with experience recruiting, hiring and managing high performing teams. A strong desire to promote growth and career development for team members.
    • Experience in the structured environment of the regulated medical device industry.  Functional familiarity with the FDA Submission process, ISO Requirements and QSR requirements is also preferred.
    • Demonstrated leadership and the ability to foster a culture of high quality designs, collaboration, and innovation.
    • Drive to ensure cooperative and open communication processes occur within and across functional groups.
    • Ability to manage budgets as related to annual operating plan targets.



    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.


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