Firmware Engineer
Nevro
At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible.
Nevro Corp., a subsidiary of Globus Medical Inc., is a global medical device company focused on delivering comprehensive, life-changing solutions that continue to set the standard for enduring patient outcomes in the treatment of chronic pain. Nevro's comprehensive HFX™ spinal cord stimulation (SCS) platform includes the Senza® SCS system and support services for the treatment of chronic pain of the trunk and limb and painful diabetic neuropathy. Nevro also provides minimally invasive treatment options for patients suffering from chronic sacroiliac joint pain.
- Develops embedded and PC-based software, which interacts with devices such as an implantable stimulator or wand. Development activities include definition of requirements, design and implementation, and verification and validation.
- Debug and analyze 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 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.
- Responsible for planning, developing, coordinating, and directing significant engineering development or a number of small projects with many complex features, utilizing internal and external resources.
- Guides the transition of advanced technologies into final products. Works closely with other product development team members to assure that their designs interface properly with other system components and to ensure that the overall system meets its performance requirements.
- Assesses new 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.
- Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies.
- Ensures Compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role.
- Represents the company in a professional manner and uphold the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties.
- B.S. in Computer Engineering, Electrical Engineering, or similar degree.
- Must have 3-5 experience in software design for embedded systems is required.
- Knowledge of C and an understanding of embedded firmware are required.
- Experience in working in a high-reliability field such as automotive, aeronautical or medical is highly preferred.
- Hands-on experience with oscilloscopes, bus analyzers and logic analyzers is also required.
- Knowledge of Assembly, C++, C# and other relevant development languages is also desired.
- Hands on experience with ARM microcontrollers and wireless communication technology is preferred.
- It is preferred that this candidate has experience in implantable medical device development.
- Functional familiarity with the FDA Submission process, ISO Requirements and QSR requirements is also preferred.
- Required to sit; climb or balance; and stoop, kneel, crouch or crawl
- Required to regularly lift and/or move up to 10 pounds, and occasionally lift and/or move up to 25 pounds
- Required to possess specific visons abilities, including: close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus.
- Passionate about Innovation : Improving patient care by delivering advanced technology to our customers is at the core of what we do. We are passionate in our role in improving the lives of patients by continuously developing better solutions.
- Customer Focused : We listen to our customers' needs and respond with a sense of urgency.
- Teamwork : Working together, anything is possible. We value every person on our team and treat each other with respect. We are accountable to one another and support each other. Together, we make each other stronger.
- Driven : We pursue our mission with energy and passion. We are nimble, results-oriented and decisive. We overcome obstacles that arise in our quest to deliver solutions that will improve the lives of our customers and patients.
Equal Employment Opportunity: Globus Medical is an equal opportunity employer. All applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, age, disability, marital status, pregnancy, national origin or citizenship. We are committed to a diverse workforce. We value all employees' talents and support an environment that is inclusive and respectful. Other Duties: Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.
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