Job Listings

Nevro is seeking an experienced and energetic Sr HRBP / Manager HRBP to support our Costa Rica leadership team. In this role, you will deliver the full range of the People life cycle on both a strategic and tactical basis to support your clients and team members. You will partner with your clients to take their business objectives and align our People programs to ensure the best outcomes.  You will be responsible for driving the People program as well as educating your clients.  You will work with our HR leadership team and operations team on the development of some of our programs we deliver to our clients; including but not limited to Performance Management, Compensation, Talent Management, and Employee Relations.    The HRBP will possess strong interpersonal skills and have the ability to build solid relationships based on trust. This role demands partnering closely with business leaders at all levels, HR leadership, and employees throughout the org to ensure our People programs and processes drive and support our business objectives. The ideal candidate will be someone who likes to be strategic and roll-up their sleeves and do great work.  The HRBP role will continue to evolve and change as the company grows and as the People organization changes along with it to meet the business needs. The ideal candidate will thrive in a dynamic and changing environment and have fun while making a difference. This position will be reporting into Nevro’s CHRO and will be located on-site in Nevro Costa Rica. - Engage and influence functional leaders as you develop and lead Nevro’s People strategy, programs and processes for the team; Influence and build relationships with people around the business. - Provide leadership for the implementation of HR programs, policies, and processes across client group.  - Partner with other HRBPs and our HR Operations functional teams on the Employee Life Cycle – including but not limited to Talent Acquisition, Compensation, Performance, and Talent Management programs, policies, processes and best practices. - Partner with our client groups on cross-functional projects, policies and practices. - Build strong relationships with the client teams at all levels. - Collaborate with others to assess, create and implement solutions for client groups. - Be well-versed in HR best practices and look for continuous improvement at all times. - Be the leader in playing a key leadership role in designing and implementing change programs. - Work with all levels of managers and employees to address various employee relations issues, working them through to resolution, while ensuring fair and equitable outcomes. - Review and analyze various business and HR metrics including data to enhance decision making, recommendations for change, and systemic improvements. - Design and implement enterprise-wide strategies to resolve organizational challenges. - Adapt to and effectively manage change and transformation. - Communicate corporate culture. - Other duties as assigned.

Nevro Corp. has a need for a Quality Test Engineer II with a strong electro-mechanical engineering background. In this role, the candidate will Evaluates the electrical and mechanical characteristics of systems and/or integrated circuits, components, sub-components and systems to determine the cause of failure, including the verification of analog and digital performance. Analyzes failure reports and recommends corrective action. Develops methods, processes, and procedures that will improve the failure analysis process and/or reduce failures. This is an internal customer facing position that requires good listening, verbal and written communication skills in order to accurately present technical.   - Manage and maintain the product investigation lab - Collaborate with appropriate technical, Clinical, Field/Sales and/or returned product analysis employees to ensure complaint investigations are adequate, accurate, detailed and timely. - Analyze product complaints. Confirm complaint and determines root causes, when possible. - Adapt or refine test procedures to properly address customer complaints - Design and develop test equipment and test specification - Differentiate between hardware and software failures. - Perform board level circuit analysis - Identify failure modes and root cause  

The Sales Representative (SR) is responsible for the achievement of sales revenue targets for the company and manages all resources to that end. This includes overseeing and leading the identification of business opportunities, building and fostering client relationships, and ensuring the effective sales of NEVRO’s products to meet/exceed sales forecasts and goals. This position reports directly to the Regional Sales Director (RSD).   - Grow the business through the education of current and new referral sources on the benefits of HF10 for the treatment of PDN. - Develop and act on a business plan which identifies opportunities to grow the referral customer base and help formulate sales strategies to meet/exceed sales goals. - Collaborate with US Sales counterparts to ensure the highest level of service with patient outcomes held in the highest regard. - Track metrics, understand trends, and create and implement strategies to maintain the growth trajectory of the business. - Positively positioning products and services to existing and new clients in the region. - Develop and implement strategies to counter competitors. - Identify, establish and maintain productive working relationships with key decision makers, customers and their staff, etc. - Train and educate customers on the merits and proper clinical usage of company products by giving presentations and demonstrations using appropriate formats and platforms (e.g., slides, manuals, etc.) to keep customers abreast of new and existing products. - Probe to understand and confirm customers’ needs, handle objections and gain commitment. - Adhere to fiscal budget for territory. - Asset/inventory management. - Report on sales process, market conditions, and customer activities to sales leader. - Utilize internal platforms to ensure flawless execution of product delivery to clients and patients. - Plan, coordinate, and execute local educational and sales events, with the support of other internal resources, intended to augment the business and help to deliver assigned sales goals. - Respond to customer needs regarding products and service by developing creative and feasible solutions or working with other related personnel (e.g., sales, clinical, research, marketing, technical support) to develop optimal solutions. - Represent company at industry conferences and maximize potential by targeting specific customers to gain sales leads and pursue opportunities to promote the company’s product range. - Develop and maintain productive working relationships within company to ensure maximum sales support and maintain a high level of customer service. - Contribute to the development of a strong team effort. - Recognize and understand competitive products, features, strengths in relation to the company’s products. - Travel daily within territory. - Other duties as assigned.

The HFX Coach, part of the patient success team, plays an important role in ensuring superior outcomes with Nevro’s therapy.  The HFX Coach interacts with patients to provide technical and product expertise.  The position is part of the Customer Excellence group and will work in collaboration with Sales Representatives, Therapy Consultants, and internal teams.   - Ability to effectively communicate directly with patients verbally by phone or email. - Serve as a resource for clinical patient support for issues relating to device troubleshooting, and Company product inquires. - Provide exceptional clinical education on Company products and related procedures while responding to detailed technical inquiries from patients. - Respond to all patient and field communications in a timely manner. Responsible for reporting all complaints regarding products to the appropriate Company personnel within the required time frames. - Provide appropriately documented follow-up on all patient interactions to the sales team. Consult with other internal Nevro departments when needed to maintain solid clinical outcomes. - Perform continued patient follow-up to assure optimal patient outcomes. - Strong analytical skills and proficiency in the use of modern computer technology and software. - Travel 5-10% for training, conferences and occasional field support. - Other duties as assigned.

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 conjunction with the DSM.  - Responsible for specified target accounts provided by DSM and RSD. - Provide forecast for targeted accounts with DSM guidance. - Prospecting for new customers, driving lead follow-up, and positively positioning our products and services to existing and new clients in the region. - Identify, establish and maintain productive working relationships with key decision makers, customers and their staff, administrative staff, etc. - Provide clinical support for DSM (programming, reprogramming, educating clients and patients, case coverage, etc.). - Build strong relationships with key clients. - Train and educate customers on the merits and proper clinical usage of company products by giving presentations and demonstrations using appropriate formats and platforms (e.g., slides, manuals, etc.) to keep customers abreast of new and existing products. - Report on sales process, market conditions, and customer activities to sales leader. - Utilize internal platforms to ensure flawless execution of product delivery to clients and patients. - Plan, coordinate and execute local educational and sales events, with the support of other internal resources, intended to augment the business and help to deliver assigned sales goals. - Other duties as assigned  

The HFX Coach, part of the patient success team, plays an important role in ensuring superior outcomes with Nevro’s therapy.  The HFX Coach interacts with patients to provide technical and product expertise.  The position is part of the Customer Excellence group and will work in collaboration with Sales Representatives, Therapy Consultants, and internal teams.   - Ability to effectively communicate directly with patients verbally by phone or email. - Serve as a resource for clinical patient support for issues relating to device troubleshooting, and Company product inquires. - Provide exceptional clinical education on Company products and related procedures while responding to detailed technical inquiries from patients. - Respond to all patient and field communications in a timely manner. Responsible for reporting all complaints regarding products to the appropriate Company personnel within the required time frames. - Provide appropriately documented follow-up on all patient interactions to the sales team. Consult with other internal Nevro departments when needed to maintain solid clinical outcomes. - Perform continued patient follow-up to assure optimal patient outcomes. - Strong analytical skills and proficiency in the use of modern computer technology and software. - Travel 5-10% for training, conferences and occasional field support. - Other duties as assigned.

This position will report to the Director of Finance and will focus on ensuring accurate financial reporting and compliance with generally accepted accounting principles and regulatory requirements. This role handles significant data analysis. The ideal candidate will have a solid operational background in the accounting function dealing with high levels of operational complexity and transaction volume. The responsibilities of this role include:   - Provide input to ensure accounting systems and processes are continually streamlined via process improvement to achieve greater efficiencies and accuracy. - Ensure accuracy and completeness of financial statements, including monthly, quarterly, and annual reporting. - Prepare the consolidated Statements of Cash Flows. - Review the roll-forward of transactions for equity awards. - Manage and review tax schedules with external tax consultants and ensure that all tax filings are accurate and timely. - Manage the annual 401(k) audit to ensure compliance with regulatory requirements. - Help manage foreign subsidiary audits. - Roll forward and update various quarterly accounting memos. - Review access levels for our ERP and the banking applications. - Complete quarterly debt compliance analysis worksheets. - Perform quarterly EPS calculations - Review and tie out quarterly earnings release and earnings script - Assist with the corporate insurance application process, ensuring that stakeholders complete all necessary documents and information to meet the application deadlines. - Assist with the detailed review of financial information used for external reporting. - Assist in the other projects as needed.

Work directly with management and other clinical research personnel to ensure the successful conduct of clinical projects, and to satisfy applicable regulatory standards and Nevro internal requirements for clinical studies.   - Assist Senior Clinical Research Associates (SCRA) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines - Provide assistance in specific tasks relating to the preparation of the project (e.g. preparation of protocols, ICF, preparation of planning documents, BIMO preparation) - Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation - Track study progress using study tracking tools, ensuring timely and quality updates - Manage and maintain Clinical Investigational Study Files to ensure the conduct of the trial is compliant with the currently approved protocol/amendment(s), with GCP, and with applicable regulatory requirements, and SOPs - Perform periodic audits of clinical study files for completeness - Oversee the organization and distribution of clinical study materials (e.g. site and patient binders, enrollment tools) working with study sites to ensure needs are fulfilled - Create and review reports for investigator compensation payments and reimbursements. - Assist in the development of any necessary tools to allow studies to proceed expeditiously (e.g. newsletter, payments, IRB, monitoring trackers) - Ensure compliance with the sponsor's responsibility to provide any new information to the investigator during the course of the study - Accompany SCRA on site visits to assist with clinical monitoring tasks - Assist SCRA to verify study data on source documentation and case report forms (CRFs) to ensure compliance with the study protocol, ICH GCPs, and SOPs. - Help identify and resolve data discrepancies to support data review in a timely manner - Other duties as assigned.  

The Salesforce Administrator IT Commercial Support will have primary responsibility for maintaining existing production modules of Salesforce, SMS and reporting to support upstream and downstream impacts. This position is expected to be a partner with the business functions and contribute to quickly resolving issues as they arise. The ideal candidate will have an in-depth knowledge and experience in all Salesforce Platforms (e.g. Salesforce Sales Cloud, Health Cloud, Community Cloud and a nice to have in Marketing Cloud). Experience in understanding and differentiating urgent issues to resolve them quickly. Strong communication and documentation skills. Additionally, experience in working with third party solutions and making recommendations. In depth experience in commercial SaaS-based applications such as Salesforce, Jira and a knowledge of new technologies and systems for commercial functions is desired. Major Responsibilities include: - Ensure customer service is timely and accurate on a daily basis - Follow up with customers to identify areas of improvement - In depth knowledge of supporting tickets through Jira Service Desk - Provide day-to-day Salesforce Sales Cloud and Health Cloud Production Support by troubleshooting issues brought up by end-users as well as other team members - Resolve issues in a timely manner - Ensure that the applications and functionality deployed into the production environment is up and running at all times - Conduct assessment on current state production systems, support and maintenance capabilities, processes and procedures, and Identify production risks and areas for improvement - Prioritize, design and facilitate successful implementation and adoption of new support and maintenance capabilities, processes and procedures - Collaborate with team members to design, configure/develop and deliver scalable Salesforce solutions based on requirements from stakeholders on Salesforce Health Cloud platform with features such as custom objects and fields, workflows, approval processes, process builder and Lightning flows - Configure and maintain record types, fields, page layouts, formulas, data validation rules, triggers, installed packages, etc. within Salesforce - Maintain user roles and profiles, security settings, access settings, etc. (User Profiles, Role Hierarchy, Sharing Rules and Security) - Lead, contribute and/or participate in CI/CD build pipeline implementation - Maintain system documentation and Salesforce policies and procedures - Provide environments management and support - Enforce Salesforce security best practices and SOX Compliance procedures

The Systems 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. - Serves as a technical test lead for verification test efforts, including owning and optimizing system, sub-system, and module verification and validation efforts to ensure complete system coverage, proper tracing, and buy-in from cross-functional stakeholders - Interacts with R&D, Quality Engineering, and Regulatory to create test strategies that have optimal amount of testing and to release technical documentation, such as engineering reports, verification plans, procedures and reports, and validation plans and reports, through doc control - Reviews and evaluates product requirements for correctness, completeness, and testability - Owns test descriptions and protocols, ensures comprehensiveness of test coverage - Participates in system integration testing activities and troubleshooting of technical issues, working with developers to identify root cause and viable resolutions - Tracks defects, validates bug fixes, analyzes bug trends, and proactively works towards catching issues early - Completes regression, dry, and formal verification runs for multiple firmware and software releases at appropriate times in the development cycle - Supports validation efforts to ensure complete system coverage - Designs, builds, executes, and maintains a test automation framework and scripts for testing mobile and web applications within a CI/CD pipeline. - Implements solutions to make the automation framework efficient and scalable. - Matures and evolves test architecture through the evaluation and adoption of new automation tools, techniques, and practices. - 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. - Provides estimates for verification effort and resources required, generates metrics, and provides periodic status updates to broader team and management as necessary. - Leads verification for a project of medium to high complexity including managing tasks for a small team of verification engineers. - Perform other duties as required 

The Systems 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 provides 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 cause 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 defect 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.

The Sales Representative (SR) is responsible for the achievement of sales revenue targets for the company and manages all resources to that end. This includes overseeing and leading the identification of business opportunities, building and fostering client relationships, and ensuring the effective sales of NEVRO’s products to meet/exceed sales forecasts and goals. This position reports directly to the Regional Sales Director (RSD).   - Grow the business through the education of current and new referral sources on the benefits of HF10 for the treatment of PDN. - Develop and act on a business plan which identifies opportunities to grow the referral customer base and help formulate sales strategies to meet/exceed sales goals. - Collaborate with US Sales counterparts to ensure the highest level of service with patient outcomes held in the highest regard. - Track metrics, understand trends, and create and implement strategies to maintain the growth trajectory of the business. - Positively positioning products and services to existing and new clients in the region. - Develop and implement strategies to counter competitors. - Identify, establish and maintain productive working relationships with key decision makers, customers and their staff, etc. - Train and educate customers on the merits and proper clinical usage of company products by giving presentations and demonstrations using appropriate formats and platforms (e.g., slides, manuals, etc.) to keep customers abreast of new and existing products. - Probe to understand and confirm customers’ needs, handle objections and gain commitment. - Adhere to fiscal budget for territory. - Asset/inventory management. - Report on sales process, market conditions, and customer activities to sales leader. - Utilize internal platforms to ensure flawless execution of product delivery to clients and patients. - Plan, coordinate, and execute local educational and sales events, with the support of other internal resources, intended to augment the business and help to deliver assigned sales goals. - Respond to customer needs regarding products and service by developing creative and feasible solutions or working with other related personnel (e.g., sales, clinical, research, marketing, technical support) to develop optimal solutions. - Represent company at industry conferences and maximize potential by targeting specific customers to gain sales leads and pursue opportunities to promote the company’s product range. - Develop and maintain productive working relationships within company to ensure maximum sales support and maintain a high level of customer service. - Contribute to the development of a strong team effort. - Recognize and understand competitive products, features, strengths in relation to the company’s products. - Travel daily within territory. - Other 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. - Serves as a technical test lead for verification test efforts, including owning and optimizing system, sub-system, and module verification and validation efforts to ensure complete system coverage, proper tracing and buy-in from cross-functional stakeholders - Interacts with R&D, Quality Engineering, and Regulatory to create test strategies that have optimal amount of testing and to release technical documentation, such as engineering reports, verification plans, procedures and reports, and validation plans and reports, through document control - Reviews and evaluates product requirements for correctness, completeness, and testability - Owns test descriptions and protocols, ensures comprehensiveness of test coverage - Participates in system integration testing activities and troubleshooting of technical issues, working with developers to identify root cause and viable resolutions - Tracks defects, validates bug fixes, analyzes bug trends, and proactively works towards catching issues early - Completes regression, dry, and formal verification runs for multiple firmware and software releases at appropriate times in the development cycle - Supports validation efforts to ensure complete system coverage - Designs, builds, executes, and maintains a test automation framework and scripts for testing mobile and web applications within a CI/CD pipeline. - Implements solutions to make the automation framework efficient and scalable. - Matures and evolves test architecture through the evaluation and adoption of new automation tools, techniques, and practices. - 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. - Provides estimates for verification effort and resources required, generates metrics, and provides periodic status updates to broader team and management as necessary. - Leads verification for a project of medium to high complexity including managing tasks for a small team of verification engineers. - Perform other duties as required 

The Sr. Software Quality Engineer is responsible for the design and development Quality Assurance activities related to new software products. This is a hands-on role where the Sr. Software Quality Engineer will apply diversified knowledge of software design and development as per 62304, software verification, recognized software development standards and quality principles and practices for implantable medical devices and accessories. This position will report to Associate Director, Quality Engineering.   - Follow procedures to guide software and systems development and ensure best engineering practice compliance with relevant regulatory requirements - Lead in the effective application, compliance, and continuous improvement of policies, procedures, and practices related to software development and validation across software teams, including: - Risk Management - Cyber security Risk assessment - Systems Validation - Quality Investigations - Traceability - Software Design - Participate in cybersecurity, post market vulnerability assessments and other risk management processes - Support internal and external regulatory audits, and other quality assurance functions. - Define or identify potential compliance gaps and assess new regulations against existing or new software and computer systems. - Demonstrate understanding of software best practices - Work with departments to discuss system gaps, fixes, design solutions and risks. - Perform other duties as required

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 provides 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 cause 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.

The Sr. Software Quality Engineer is responsible for the design and development Quality Assurance activities related to new software products. This is a hands-on role where the Sr. Software Quality Engineer will apply diversified knowledge of software design and development as per 62304, software verification, recognized software development standards and quality principles and practices for implantable medical devices and accessories. This position will report to Associate Director, Quality Engineering.   - Follow procedures to guide software and systems development and ensure best engineering practice compliance with relevant regulatory requirements - Lead in the effective application, compliance, and continuous improvement of policies, procedures, and practices related to software development and validation across software teams, including: - Risk Management - Cyber security Risk assessment - Systems Validation - Quality Investigations - Traceability - Software Design - Participate in cybersecurity, post market vulnerability assessments and other risk management processes - Support internal and external regulatory audits, and other quality assurance functions. - Define or identify potential compliance gaps and assess new regulations against existing or new software and computer systems. - Demonstrate understanding of software best practices - Work with departments to discuss system gaps, fixes, design solutions and risks. - Perform other duties as required

This position plays a key role in the development of Class III implantable Neuromodulation systems. This is a technical management position that reports to the Director of Systems Engineering. - Manage the software verification team (supports verification for Windows software, iOS and Android mobile app software) including but not limited to engineers, technicians, and external vendors. - Drive accountability, consistency, quality, standardization, and discipline across the product development - Manage verification for complex medical device development programs from concept through requirements, design, implementation, verification, and - Work with other verification team managers or leads to establish best practices to optimize system, sub-system, and module verification efforts to ensure complete system verification coverage. - Drive team to perform software level verification against requirements, performing hands-on system integration testing, troubleshooting of technical issues, and development of test plans, procedures, and reports. - Work cross-functionally with Marketing, Quality, Engineering, Regulatory, Manufacturing, and Clinical, to resolve technical product issues found during integration, verification, and validation. - Take a leadership position in development processes, efficient use of prototyping resources, standards and methodologies, and prioritization of business objectives. - Build functional bench strength – includes staffing, training, completing performance evaluations and actively supporting career development for future department and business leaders. - Perform other duties as required 

As a Senior Regulatory Affairs Manager, you will lead a team of regulatory professionals to develop global regulatory strategies and submissions activities for various new development and product modification projects. Responsibilities will involve collaboration with R&D, Clinical, Quality and other required functions to execute regulatory strategy from product inception to product launch.   - Develop, document and implement regulatory strategies for new technologies and product modifications. - Prepare IDE, 510(k), PMA, CE Mark submissions and other related regulatory filings. - Establish and maintain a professional image and lead communications with FDA, Notified Bodies, and other regulatory agencies. - Interface with FDA, Notified Bodies, and other regulatory agencies regarding regulatory submission strategy and approval reviews. - Represent Regulatory Affairs on cross functional new development teams and provide leadership and regulatory guidance for the support of new product development projects and product modifications. - Collaborate with cross functional teams to develop clinical trial plans and reports which support clinical indication expansion projects. - Collaborate with R&D and Quality to determine and execute pre-clinical test plans in support of new product development regulatory submissions. - Provide leadership and regulatory guidance to ensure that documentation for regulatory submissions are accurate and timely to support submission timelines. - Maintain current knowledge of competitive technologies in addition to medical and technical developments related to the company’s products. - Lead a team of regulatory professionals and ensure all assigned project goals are met. - Manage consultants and their contracts for assigned regulatory projects. - Act as advisor to subordinate(s) to meet schedules and/or resolve technical problems - Mentor subordinates, identify development plans and ensure an environment of encouragement and support to allow them to develop to their true potential. - Lead improvements in regulatory procedures and processes. - Ensure new regulations or changes to existing regulations are communicated throughout the organization through company policies, procedures, and training. - Review product labeling and promotional material to ensure compliance with relevant regulatory requirements. - Provide regulatory support for internal and external audits - Other duties as assigned.  

  The Senior Manager, Healthcare Professional (HCP) Marketing will represent marketing in the development, implementation and management of marketing programs. He/she will develop commercial plans and marketing/sales materials as Nevro expands indications and patient populations, leading marketing content and strategy to support professional education, conferences and HCP digital marketing. This position will develop and launch downstream programs to the US sales team. - Drive New Product Adoption, including exploration of HCP benefit and partnering with cross-functional teams to design, develop and deliver new product toolkits - Gather, synthesize, and prioritize voice of customer feedback from physicians and other stakeholders to identify new opportunities, prioritize and drive alignment across the organization - Establish metrics and manage ongoing continuous improvement of marketing programs and materials - Analyze business to understand trends and drive recommendations to improve execution of strategic plans - Collaborate closely with Sales, Professional Education and cross-functional partners to support and accelerate product adoption - Develop and maintain strong relationships with key opinion leaders and key customers - Partner with Learning & Development to ensure the effective training of the sales team - Develop and maintain relationships with key strategic partners - Other duties as assigned

In this important role, you will assist the Digital Health team in taking Nevro to the next level, along with your career.  You will participate in research and product development activities ranging from product concept through transfer to manufacturing. You will collaborate with other driven technology professionals and designers, contributing your Android developer expertise to our team as you stay abreast of new and changing technologies, another passion of yours. Experience the best of both worlds – cutting edge med tech and transforming patient experiences by helping execute end-to-end human-centered products and services. You will apply knowledge of engineering principles and practices for software development for implantable medical devices and accessories. - Review and approve the design and development of the Mobile app, incorporating feedback from Product Management, User Experience, Architecture, and Quality Engineering. - Collaborate with back-end application developers to design and refine APIs for sending and retrieving data to and from the mobile application. - Develop and maintain test frameworks and interactive testing, including working with beta testers. - Instrument with analytics to understand and communicate usage and adoption models of the app. - Provide subject matter expertise on mobile design practices, from experience to stability and performance. Mobile is different, and you need to know why and be able to drive a viewpoint. - 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. - 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 - Other duties as assigned