Sr Electrical Engineer

Globus Medical Inc; Redwood City (CA); Sur place; USD 150 000 - 190 000; Plein temps

Résumé du poste

NML Medical seeks a Sr. Electrical Engineer to lead design and development of Class III implantable neuromodulation systems for deep brain stimulation.

You will guide electrical components, mentor teams, and drive reliability and manufacturability while ensuring compliance with design controls and regulatory standards. The role calls for deep expertise in embedded systems, mixed-signal circuits, power management, and hardware verification, with collaboration across systems, firmware, mechanical,

Qualifications

• Bachelor’s degree with 8 years of related experience in medical device development or verification.
• Master’s degree with 6 years of related experience.
• PhD with 3 years of related experience.

Responsabilités

• Lead design and development of Class III implantable neuromodulation systems and test fixtures.
• Own schematic design, PCB layout, BOMs, and system integration across development stages.
• Validate concepts with experiments and generate design data for verification.
• Collaborate with cross-functional teams to ensure FDA/regulatory alignment and design controls.

Connaissances

Embedded system design

Mixed-signal electronics

Power electronics

FMEA/risk management

Formation

Bachelor’s degree (8+ yrs)

Master’s degree (6+ yrs)

PhD (3+ yrs)

Description du poste

Position Summary:

The Sr. Electrical Engineer plays a key leadership role in the design and development of a Class III implantable neuromodulation system for deep brain stimulation (DBS). In this role, you will be leading the technical team to make key and impactful decisions for electrical components in the system. 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:

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 electrical product requirements and specifications 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. Train and mentor contract manufacturing engineers and technicians on product testing and troubleshooting methods. Participates in the design and execution of verification testing protocols, methods and reports to ensure products meet design requirements Supports risk management documentation including hazard analysis and failure modes and effect analysis (FMEA) to identify and mitigate design and process risks Partner closely with system, firmware, mechanical, and test engineering teams to ensure full system integration and performance alignment. Contribute to the company’s intellectual property portfolio through innovative concepts and technical disclosures. Operate in compliance with design controls and quality system procedures. Prepare technical reports, presentations, and design reviews for management and cross-functional stakeholders. Communicate with physicians and other clinicians on product design and development activities and gather feedback on product prototypes Collaborate with Marketing, Regulatory, and Quality to ensure design inputs and verification activities align with product and business 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 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.) Strong analytical and problem-solving skills. Strong communication and presentation skills with the ability to influence cross-functional decisions. Ability to thrive in a fast-paced, multidisciplinary environment. Ability to travel approximately 10% of the time domestically and internationally. Strong expertise in embedded system design, mixed-signal electronics, and power electronics. Understands and can operate within a highly regulated environment following industry technical and test standards as well as good documentation and laboratory practices. Highly self-directed; determines and pursues courses of action necessary to achieve desired results. Often initiates assignments independently. Demonstrated ability to plan, develop, coordinate, and direct significant engineering programs or multiple smaller projects with complex features, leveraging both internal and external resources. Applies advanced technical principles, theories, and concepts to solve complex problems, while developing new methodologies and approaches that deliver innovative and ingenious solutions. Proactively identifies developmental risks and communicates mitigation strategies effectively to management. Fosters a culture of collaboration and open communication across all levels of the organization. Serve as a technical consultant to the project team, helping solve challenging design issues, providing training, and bridging knowledge across disciplines. Working familiarity with FDA submission processes, ISO standards (13485), and Quality System Regulation (QSR) requirements. Experience working with relevant product development standards, guidelines, and regulations (60601, 14708, 14971, FCC) Experienced in software engineering, with the ability to guide firmware development or create hardware-characterization tools (languages such as C, Assembly, and Python).

Physical Demands:

The physical demands listed here are representative of those that must be met by and employee to successfully perform the essential functions of this job. 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.

Our Values:

Our Life Moves Us philosophy is built on four values: Passionate About Innovation, Customer Focused, Teamwork, and Driven. 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. 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.