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The Application Engineer is a general software engineer with a specialty in PC-based development. The are expected to participate in research and product development activities ranging from product concept through transfer to manufacturing and deployment and upgrade of computers in the field. This position will apply knowledge of engineering principles and practices for software development of implantable medical devices and accessories.   Role Requirements - Develops embedded and PC-based software, which interact with devices such as an implantable stimulator. - Development activities include requirements definition, design, implementation, and verification / validation. - Debugging and analyzing device issues and field returns. - Develops software in a regulated environment in accordance with internal operating procedures and external standards and regulations. - Conducts cross-functional reviews of the software at appropriate times in the development cycle.  - With direction, determines and pursues courses of action necessary to obtain desired results. - Applies technical principles, theories, and concepts, in addition to developing new principles and concepts towards the solution of complex technical problems and provides solutions which are innovative and ingenious. - Proactively identifies areas of developmental risk and communicates these to the team accordingly. - Works in accordance with quality system procedures and actively enforces its objectives.  - Other duties as assigned 

The Research Engineer is responsible for investigating and implementing the technical and clinical requirements of the Product Research and Emerging Clinical Indications team. Under the direction of the senior members of the team, the research engineer will also research and investigate disruptive technical and clinical opportunities including developing clinical models of efficacy. He/she will be responsible for the tactical implementation of the program and projects within the team. - Assists in the investigate novel, disruptive technologies, and clinical therapies - Assists in the exploration and evaluation of external technical and clinical opportunities and performing assessments, recommendations and technical due diligence - Works closely with other team members in designing experimental protocols, as well as the conducting and monitoring these research projects, and interpretation of results - Participates in the development and writing of integrated reports and preparation of presentations and manuscripts of scientific meetings and technical journals - Participates in design and writing of protocols, case report forms and informed consent forms for clinical studies - Performs a variety of analysis in the collection, verification, analysis, documentation and interpretation of research data - Evaluates and interprets collected data, and prepares presentations, reports and analyses describing progress, trends, and recommendations or conclusions - Identify, assess, recommend, and integrate novel technologies and/or clinical therapies - Conduct descriptive and exploratory analysis of technical and clinical data - Define statistical tests and methods for both evaluating and generating statistical hypotheses - Work cross-functionally (e.g., business development, engineering, marketing, clinical affairs, quality, and legal) as needed to assess potential opportunities - Other duties as assigned.    

- Lead the development of major features and architectural enhancements for the Nevro R&D Care Team Applications group, primarily for web services and web applications using Microsoft .Net Core, React, Terraform, and other technologies. Activities include: - - Working with the cross-functional teams to define software requirements. - Designing data models, data flows, software components, and (as needed to extend existing implementations) cloud infrastructure architecture. - Implementation of software and cloud infrastructure in AWS, Confluent Cloud, and others. - Ensuring features are testable using automated test tooling. - Implementing unit testing and/or performing manual testing for features - Develop software in a regulated environment in accordance with internal operating procedures and external standards and regulations. - Proactively identify areas of developmental risk for projects or features and communicate these to management accordingly. - Work closely with other product development teams: ensure that their products will interface as required with the Care Team Application’s products and overall system requirements are met. - Work in accordance with quality system procedures and actively enforce its objectives. - Contribute to the intellectual property base of the Company via active communication of new concepts to Management. - Lead continuous improvement of our products, platforms, and practices: - Define and document software development best practices and ensure adherence through code reviews and training sessions as needed. - Enhance our SDLC to reduce toil or improve product quality. -  Continuously contribute to platform reliability, security, monitoring, logging.

This position plays a key role in the development of the next generation of Class III implantable Neuromodulation systems for pain management. This is a technical position that reports to a Principal Engineer, Manager, or higher organizational leader.

This position plays a key role in the development of the next generation of Class III implantable Neuromodulation system for pain management. This is a technical position that reports to the Senior Manager, Mechanical Engineering.  - Perform tasks required in medical device product development – for neuromodulation devices as well as for SI joint fusion products. - Leads small project teams to deliver cross functional solutions to technical problems. - Establish product requirements and specifications - Designs medical device components and fixtures - Update & review product CAD models and drawings and participate in Design Reviews. - Interfaces with external vendors to develop prototypes - Analyzes and documents test results in a laboratory notebook - Participates in the design of new test methods and procedures - Conducting tests and documenting test reports - Responsible for processing ECOs and other documentation in compliance with FDA guidelines and ISO requirements - Interface with other departments such as Marketing, Manufacturing, Regulatory and Quality - Communicates with physicians and other clinicians on product design and development activities and gathers feedback on product prototypes - Investigate and solve mechanical product failure modes and devise solutions to problems - Understands and can operate within a highly regulated environment with good documentation and laboratory practices. - Performs other related duties as assigned  

The Software Verification Engineer will play a key role in the development of a Class III implantable Neuromodulation system for pain management, working cross-functionally to help verify firmware, software applications, and whole systems and make sure that all stakeholders are aligned, and requirements and user needs are met. - Designs, develops, updates, executes, and debugs firmware, software, and/or system tests (manual, interactive, automated) and maintains testing metrics. - Owns and optimizes system, sub-system, and module verification and validation efforts to ensure complete system coverage and provide proper tracing. - Reviews and evaluates product requirements for correctness, completeness, and testability and analyzes and allocates a set of requirements into an appropriate set of verification tests. - Conducts and participates in cross-functional reviews of the test protocol development (test strategy, test design, test code). - Performs hands-on system integration testing and troubleshooting of technical issues, working with developers to identify root causes and viable resolutions, document issues found, and verify bug fixes of software defects. - Completes regression, dry, and formal verification runs for multiple firmware and software releases at appropriate times in the development cycle. - Tracks defects and validates bug fixes. - Owns technical documentation such as engineering reports, verification plans, procedures and reports, and validation plans and reports. - Develops and validates software and hardware-based tools to assist in development and testing. - Assesses new test technologies via reviews of the state of the art or by performing proof of concept work and communicates the results of the assessment to members of the development organization. - Other duties as assigned.

Systems Engineer, Medical Device, Redwood City, CA- Ensure the logical and systematic conversion of customer requirements and performance requirements into systems solutions that account for technical, cost and schedule constraints for RF communications systems and active implantable systems. Collaborate with cross-functional stakeholders to identify design inputs (user needs and system requirements). Evaluate technical, scheduling, and resource tradeoffs when generating requirements for project. Ensure requirements are correct, complete, unambiguous, and testable, and provide sufficient detail for tracing to subsystem and module level requirements. Document design inputs into requirements tracking system for tracking and traceability. Utilize IEC 62366, ANSI/AAMI HE75, and FDA Guidance for Human Factors and Usability Engineering. Perform human factors engineering across the product lifecycle including identification of customer user needs and use scenario, definition of use specifications (user profiles, user environments) and user interface requirements. Assist with generation of deliverables for compliance with IEC 60601, IEC 62366, IEC 62304, ISO 14708, ANSI/AAMI HE75, and FDA Guidance for Human Factors and Usability Engineering, including working with external vendors as necessary. Investigate and define systems engineering requirements for new algorithms or features. Perform Risk management using risk analysis, FMEA, or ISO 14971. Perform engineering tasks including definition, verification, or product development of a system, and drive them to on-time, high quality completion. Perform hands-on system integration testing and troubleshooting of technical issues. Perform system level verification against requirements. Create test plans, procedures and reports, perform and analyze system setup, and conduct verification and validation activities. Hybrid work is permitted per employer’s discretion. (No agencies or phone calls please.) #LI-DNI