Senior Electrical Engineer

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.  About Globus 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. Position Summary The Senior Electrical Engineer plays a key leadership role in the design and development of a Class III implantable neuromodulation system used in spinal cord injury (SCI) repair. This engineer will serve as a technical influencer, shaping electrical architecture decisions, directing cross-functional design activities, and guiding teams toward robust, scalable engineering solutions. This role will ensure electrical integrity, patient safety, and compliance with medical device regulations across the full product lifecycle. We are seeking an engineer who is passionate about precision, obsessive about quality, and motivated by a mission to deliver breakthrough, evidence-based therapies that transform patient outcomes. If you aspire to lead innovation in implantable medical technology, this is your opportunity to make an impact. Essential Functions: Electrical Design & Development Lead the design and development of Class III implantable neuromodulation systems, associated accessories, test systems, and manufacturing fixtures. Design and analyze electronic circuits, including: Embedded systems and firmware interfaces Mixed-signal analog/digital circuits Power management and charging circuits Own schematic design, PCB layout, component selection, BOMs, characterization, and system integration across all development stages. Establish and maintain electrical product requirements, specifications, and system level constraints. Design and execute experiments to validate concepts, develop new test methods, and generate design data. Characterize and verify hardware performance to ensure medical-grade precision and reliability. Drive design-for-reliability and manufacturability improvements. Regulated Product Development Support development activities in compliance with FDA regulations and ISO standards for Class III implantable medical devices. Prepare, process, and maintain engineering documentation such as ECOs, reports, and design files. Contribute to verification and validation strategy and execution for electrical subsystems. Ensure electrical design decisions meet safety, reliability, and regulatory expectations across the development lifecycle. Technical Leadership & Influence Lead cross-functional project team(s) to deliver electrical solutions aligned with program goals. Influence product architecture, system-level trade-offs, component selection, and manufacturing strategies. Anticipate electrical risks and proactively guide mitigation plans. Collaborate closely with systems, mechanical, firmware, manufacturing, quality, and regulatory teams to ensure seamless system integration. Communicate effectively with physicians and clinicians to gather user insights and integrate feedback into design decisions. Innovation & Technology Development Evaluate new components, technologies, manufacturing processes, and design methodologies to support feasibility and concept development. Support laboratory and clinical research activities by developing prototypes, fixtures, and investigational designs. Contribute to early-stage concept development and participate in intellectual property generation. Quality & Process Discipline Follow quality system procedures, documentation practices, and laboratory standards. Supports risk management documentation including hazard analysis and failure modes and effect analysis (FMEA) to identify and mitigate design and process risks. Drive continuous improvement in electrical design processes, test methods, and development workflows. Ensure all electrical deliverables meet performance, reliability, and compliance requirements. 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 upholds the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions. Qualifications: Bachelor’s degree with 8 years, Master’s degree with 6 years, or PhD with 3 years of related experience with development or verification in the medical device industry (Class III medical device experience preferred). Minimum 5 years of experience in a regulated industry; medical device experience strongly preferred. Mostly self-directed. Determines and pursues courses of action necessary to obtain desired results. (Recommendation of assignments is often self-initiated.) Ability to travel approximately 10%