Job Listings

The Therapy Consultant is the primary clinical support who works with Nevro Sales Representatives to meet existing and potential clients (e.g., physicians, physician office groups at hospitals) and patients to identify their clinical goals and constraints related to patient needs. They also provide technical expertise, product demonstrations, installation and maintenance of company products. - Promote company products to current and potential customers within a defined region by providing clinical education of implant procedures and support. -

The Therapy Consultant is the primary clinical support who works with Nevro Sales Representatives to meet existing and potential clients (e.g., physicians, physician office groups at hospitals) and patients to identify their clinical goals and constraints related to patient needs. They also provide technical expertise, product demonstrations, installation and maintenance of company products. - Promote company products to current and potential customers within a defined region by providing clinical education of implant procedures and support. -

The Associate Sales Representative (ASR) supports achievement of sales revenue targets and helps to grow market share for a specified territory by promoting, selling and servicing NEVRO products.Practice good territory management in terms of organization, administration and expense planning. Control and train appropriate medical staff on products and procedures. This is a clinical sale with strong value added focus and an emphasis on improving patient care outcomes.Account responsibility and sales development goals established by the RSD in...

Nevro Redwood City, California (onsite position)   Senior Regulatory Affairs Specialist, Redwood City, CA - Develop strategies for global approvals to introduce new Spinal cord stimulation systems to market, maintain existing products, provide advice on regulatory requirements, prepare worldwide submissions, and negotiate approval with global regulatory agencies. Support cross-functional new product development projects and prepare and compile all materials required in submissions, license renewal and annual registrations. Assist in...

- Performs warehousing operations, to include tray cleaning, tray and component receiving, tray assembly, and shipping - Ensures proper utilization of key system software for inventory management. - Ensuring compliance with warehouse related SOPs/WIs, other regulatory requirements, and all applicable company policies - Maintains a well organized and clean warehouse at all times. - Reports to Nevro KOP Warehouse...

· Support the implementation, administration, and management of company’s corporate compliance program. · Manage and support compliance audit and monitoring activities, including through data analytics, live monitoring and engagement with internal teams. · Proactively identify, review and mitigate potential areas of risk to Nevro’s business based on internal policies and industry standards.

The Therapy Consultant is the primary clinical support who works with Nevro Sales Representatives to meet existing and potential clients (e.g., physicians, physician office groups at hospitals) and patients to identify their clinical goals and constraints related to patient needs. They also provide technical expertise, product demonstrations, installation and maintenance of company products. - Promote company products to current and potential customers within a defined region by providing clinical education of implant procedures and support. -

· Provides support to the Professional Education Directors and Managers. · Helps to support Professional Educational Initiatives including cadaveric trainings, didactic events, conferences, and society meetings. · Support team on development and management of Prof Ed curriculum and content.

The Business Analyst IT Applications will have primary responsibility for creating maintaining the partnership between business needs and technology delivery. This position will be responsible for developing business requirements and related rules based on organizational needs primarily for the Sales, Marketing, Customer Excellence, and Commercial Operations departments while ensuring R&D, HR, Legal, Clinical and Regulatory and Quality departments changes are not impacting commercial processes. The Business Analyst will work closely with business partners and subject matter experts in the definition, testing, training, implementation, and support of functional...

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.

(Must currently live in the SF Bay Area)   The Senior Regulatory Affairs Specialist is responsible for developing strategies for global approvals to introduce new Spinal cord stimulation systems to market, maintain existing products, provide advice on regulatory requirements, prepare worldwide submissions, and negotiate their approval with global regulatory agencies.  -

The Business Development Manager is responsible for achieving sales revenue targets and growing market share for a specified territory by promoting, selling and servicing NEVRO products. This includes overseeing and leading the identification of new business opportunities, building and fostering client relationships, and ensuring the effective sales of NEVRO’s products to meet/exceed sales forecasts and goals.   Planning/Results Orientation

The QA Compliance Specialist I, is responsible for working cross-functionally to ensure maintenance and review of events and complaints, as set forth by the FDA and other regulatory agencies. Requires follow-up internally and externally to assure complete and accurate event files, complaint detail, and product performance information. Supports complaint handling in internal and external audits and inspections. - Perform tasks to obtain adequate information to ensure proper documentation and closure of each complaint. - Follow up with internal...

Applying knowledge of QSR and GMP requirements on a daily basis, the duties and responsibilities for this position include, but are not limited to, the following:   -

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. -

(Must live in the SF Bay Area)   The Principal Regulatory Affairs Specialist  will be part of this high-performance team and responsible for developing regulatory strategies, preparing U.S. and major market submissions and obtaining approval to introduce new spinal implants and biologics worldwide. These responsibilities are performed through the collaboration...

The Salesforce Developer IT Commercial will have the ability to translate business needs into technical specifications, design and development solutions, test and deploy them into production. Must have a passion for working cross functionally and building solutions to support business process and data flows and a strength in solving platform issues with expert troubleshooting skills. This role will work closely with our Sales, Operations, IT, Marketing, Finance, and other groups as needed.

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...

- Owns transactions recording, records accuracy and corresponding reconciliation process for Costa Rica Site General Ledger, in both, Corporative and Statutory books. - Responsible for statutory Financial Statements preparation and all relations and reporting with governmental tax and compliance authorities. - Responsible for month end close process for Statutory books. -