Sr. Systems Verification Engineer

About Nevro

Nevro (NYSE: NVRO) is a global medical device company headquartered in Redwood City, California.

We are focused on delivering comprehensive, life-changing solutions that continue to set the standard for enduring patient outcomes in chronic pain treatment. The company started with a simple mission to help more patients suffering from debilitating pain and developed its proprietary 10 kHz Therapy, an evidence-based, non-pharmacologic innovation that has impacted the lives of more than 100,000 patients globally.

Nevro's comprehensive HFX spinal cord stimulation (SCS) platform includes a Senza SCS system and support services for the treatment of chronic trunk and limb pain and painful diabetic neuropathy. Senza, Senza II, Senza Omnia, and Senza HFX iQ are the only SCS systems that deliver Nevro's proprietary 10 kHz Therapy. HFX iQ, Nevro's latest innovation, is the first and only SCS System that uses Artificial Intelligence to optimize and maintain pain relief using each patient's response1.Nevro's unique support services provide every patient with an HFX Coach throughout their pain relief journey and every physician with HFX Cloud insights for enhanced patient and practice management.

Nevro also recently added a minimally invasive treatment option for patients suffering from chronic sacroiliac joint ("SI joint") pain and now provides the most comprehensive portfolio of products in the SI joint fusion space, designed to meet the preferences of physicians and varying patient needs in order to improve outcomes and quality of life for patients.

Job Summary & Responsibilities

Senior Systems Verification Engineer, 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 the 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. Remote work permitted per employer's discretion within reasonable commuting distance. (No agencies or phone calls please.) #LI-DNI

Role Requirements

Requires Bachelor's degree in Biomedical Engineering, Electrical Engineering, Computer Engineering, or Systems Engineering and 7 years of experience as systems verification engineer, systems test engineer, quality assurance engineer or similar engineer role in the medical device industry or Master's degree in Biomedical Engineering, Electrical Engineering, Computer Engineering, or Systems Engineering and 5 years of experience as systems verification engineer, systems test engineer, quality assurance engineer or similar engineer role in the medical device industry.

Must possess 7 years of experience with a Bachelor's degree and 5 years of experience with a Master's degree in the following:

• Class II or III medical devices
• working with devices that comply with IEC 60601, ISO 14708, IEC 62304
• • Working with a cross-functional team

Must possess 4 years of experience with Performing system level verification against requirements.

Must possess 2 years of experience with scripting with high-level programming languages such as Python or PHP.

Must possess 1 year of experience with the following:

• Risk management (risk analysis, FMEA, ISO 14971)

• • RF communications systems and active implantable systems

• Testing systems with equipment including one or more of the following: oscilloscopes, power supplies, multimeters, differential probes, spectrum analyzers, Python, Bluetooth sniffer and protocol analyzer

• Managing systems verification

Target Pay Range

$148,408 to 148,408

EEO Statement

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.