I
Senior Electrical Engineer
Accepting applicationsInvestigo · Redwood City, CA
Full-Time Mid_senior MentorPythonanalogmixed-signalpower management
Posted
2d ago
Category
Verification
Experience
Mid_senior
Country
United States
Sr. Electrical Engineer – Implantable Medical Devices
We are seeking a Sr. Electrical Engineer to lead the design and development of a Class III implantable neuromodulation system for deep brain stimulation (DBS). This is an exciting opportunity for an engineer passionate about precision, quality, and innovation in medical technology. You will guide a technical team, make impactful decisions on electrical components, and drive the development of breakthrough therapies that transform patient outcomes.
Key Responsibilities:
Lead the design and development of implantable neuromodulation systems, accessories, test systems, and manufacturing fixtures.
Design and analyze electronic circuits, including embedded systems, mixed-signal analog/digital circuits, and power management/charging circuits.
Own schematic design, PCB layout, component selection, BOMs, characterization, and system integration.
Establish electrical product requirements and specifications.
Design and execute experiments to validate concepts and develop new test methods.
Characterize and verify hardware performance to ensure medical-grade precision and reliability.
Drive design-for-reliability and manufacturability improvements.
Mentor and train contract manufacturing engineers and technicians.
Participate in verification testing protocols and risk management documentation (hazard analysis, FMEA).
Collaborate with system, firmware, mechanical, and test engineering teams for full system integration.
Contribute to intellectual property through innovative concepts and technical disclosures.
Operate in compliance with design controls and quality system procedures.
Prepare technical reports, presentations, and design reviews.
Communicate with clinicians to gather feedback on product prototypes.
Collaborate with Marketing, Regulatory, and Quality to align design inputs and verification activities with business objectives.
Qualifications:
Bachelor’s degree with 8 years, Master’s with 6 years, or PhD with 3 years of related experience in medical device development or verification (Class III preferred).
Minimum 5 years in a regulated industry; medical device experience strongly preferred.
Strong expertise in embedded system design, mixed-signal electronics, and power electronics.
Experience with FDA submission processes, ISO standards (13485), QSR, and relevant product development standards (60601, 14708, 14971, FCC).
Proficiency in software engineering and firmware development (C, Assembly, Python).
Strong analytical, problem-solving, communication, and presentation skills.
Ability to thrive in a fast-paced, multidisciplinary environment.
Ability to travel up to 10% domestically and internationally.
Applicants must be legally authorized to work in the United States for any employer. Sponsorship is not available for this position now or in the future.
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We are seeking a Sr. Electrical Engineer to lead the design and development of a Class III implantable neuromodulation system for deep brain stimulation (DBS). This is an exciting opportunity for an engineer passionate about precision, quality, and innovation in medical technology. You will guide a technical team, make impactful decisions on electrical components, and drive the development of breakthrough therapies that transform patient outcomes.
Key Responsibilities:
Lead the design and development of implantable neuromodulation systems, accessories, test systems, and manufacturing fixtures.
Design and analyze electronic circuits, including embedded systems, mixed-signal analog/digital circuits, and power management/charging circuits.
Own schematic design, PCB layout, component selection, BOMs, characterization, and system integration.
Establish electrical product requirements and specifications.
Design and execute experiments to validate concepts and develop new test methods.
Characterize and verify hardware performance to ensure medical-grade precision and reliability.
Drive design-for-reliability and manufacturability improvements.
Mentor and train contract manufacturing engineers and technicians.
Participate in verification testing protocols and risk management documentation (hazard analysis, FMEA).
Collaborate with system, firmware, mechanical, and test engineering teams for full system integration.
Contribute to intellectual property through innovative concepts and technical disclosures.
Operate in compliance with design controls and quality system procedures.
Prepare technical reports, presentations, and design reviews.
Communicate with clinicians to gather feedback on product prototypes.
Collaborate with Marketing, Regulatory, and Quality to align design inputs and verification activities with business objectives.
Qualifications:
Bachelor’s degree with 8 years, Master’s with 6 years, or PhD with 3 years of related experience in medical device development or verification (Class III preferred).
Minimum 5 years in a regulated industry; medical device experience strongly preferred.
Strong expertise in embedded system design, mixed-signal electronics, and power electronics.
Experience with FDA submission processes, ISO standards (13485), QSR, and relevant product development standards (60601, 14708, 14971, FCC).
Proficiency in software engineering and firmware development (C, Assembly, Python).
Strong analytical, problem-solving, communication, and presentation skills.
Ability to thrive in a fast-paced, multidisciplinary environment.
Ability to travel up to 10% domestically and internationally.
Applicants must be legally authorized to work in the United States for any employer. Sponsorship is not available for this position now or in the future.
Show more Show less