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.
The Software Architect shall participate in research and product development activities ranging from product concept through transfer to manufacturing. This position will apply knowledge of engineering principles and practices for software development for implantable medical devices and accessories.
Develop and support REST API’s for a system that includes the following: an implantable stimulator, external stimulator, patient charger, patient-facing devices and clinician-facing devices. Development activities include definition of requirements, design and implementation, and verification and validation support.
Develops software in a regulated environment in accordance with internal operating procedures and external standards and regulations. Conducts cross-functional reviews of the software development at appropriate times in the development cycle.
Significantly self-directed. Determines and pursues courses of action necessary to obtain desired results.
Proactively identifies areas of developmental risk and communicates these to management accordingly.
Works closely with other product development team members to assure that their designs interface properly with other system components and to assure that the overall system meets its performance requirements.
Assesses new test technologies via reviews of the state of the art or by performing proof of concept work. The results of this assessment must be communicated to the software team or other members of the development organization.
Contributes to the intellectual property base of the Company via active communication of new concepts to Management.
Works in accordance with quality system procedures and actively enforces its objectives.
B.S. in Computer Science, or equivalent years of experience may be substituted for the degree requirement.
A minimum of 12+ years’ experience in software design and development for REST API’s is desired.
Candidate must be proficient with API application development using .NET for backend web services.
It is highly preferred that this candidate has experience with medical software development or development in an equivalent regulated environment.
Functional familiarity with the FDA Submission process, ISO Requirements and QSR requirements is also preferred.