4 ΡΠ°ΡΠ° Π½Π°Π·Π°Π΄
Sr Electrical Engineer (Medical Devices)
ΠΡΡΡ & Π‘ΠΎΠΏΡΠΎΠ²ΠΎΠ΄
ΠΠ»Ρ ΠΌΡΡΡΠ° Ρ ΡΡΠΎΠΉ Π²Π°ΠΊΠ°Π½ΡΠΈΠ΅ΠΉ Π½ΡΠΆΠ΅Π½ Plus
ΠΠΏΠΈΡΠ°Π½ΠΈΠ΅ Π²Π°ΠΊΠ°Π½ΡΠΈΠΈ
Π’Π΅ΠΊΡΡ:
TL;DR
Sr Electrical Engineer (Medical Devices): Leading the design and development of Class III implantable neuromodulation systems for deep brain stimulation with an accent on embedded systems, mixed-signal electronics, power management, and medical-grade reliability. Focus on designing and verifying complex hardware, managing risk and design controls, and integrating electrical systems with firmware, mechanical, and test engineering.
Location: Redwood City, California, United States
Company
develops medical technologies and evidence-based therapies that improve surgical techniques and outcomes for patients with musculoskeletal disorders.
What you will do
- Lead the design and development of Class III implantable neuromodulation systems for deep brain stimulation, accessories, test systems, and manufacturing fixtures.
- Design and analyze embedded, mixed-signal analog/digital, power management, and charging circuits.
- Own schematics, PCB layout, component selection, bills of materials, hardware characterization, and system integration.
- Establish electrical requirements, design experiments, develop test methods, and execute verification activities.
- Drive reliability and manufacturability improvements, risk mitigation, and compliance with design controls and quality procedures.
- Collaborate with firmware, mechanical, test, regulatory, quality, marketing, physicians, and clinicians on product development and technical reviews.
Requirements
- Bachelorβs degree with 8 years, Masterβs degree with 6 years, or PhD with 3 years of related medical device development or verification experience.
- At least 5 years of experience in a regulated industry; Class III medical device experience is strongly preferred.
- Strong expertise in embedded system design, mixed-signal electronics, and power electronics.
- Experience with FDA submission processes, ISO 13485, Quality System Regulation, and standards including 60601, 14708, 14971, and FCC.
- Ability to plan and direct significant engineering programs or multiple complex projects, solve advanced technical problems, and communicate effectively across disciplines.
- Software engineering experience with the ability to guide firmware development or create hardware-characterization tools using languages such as C, Assembly, and Python.
Nice to have
- Class III medical device development experience.
Culture & Benefits
- Full-time employment in a multidisciplinary medical technology environment.
- Approximately 10% domestic and international travel.
- Values-driven culture focused on innovation, customer focus, teamwork, and decisive execution.
- Equal opportunity and inclusive workplace commitment.
ΠΡΠ΄ΡΡΠ΅ ΠΎΡΡΠΎΡΠΎΠΆΠ½Ρ: Π΅ΡΠ»ΠΈ ΡΠ°Π±ΠΎΡΠΎΠ΄Π°ΡΠ΅Π»Ρ ΠΏΡΠΎΡΠΈΡ Π²ΠΎΠΉΡΠΈ Π² ΠΈΡ ΡΠΈΡΡΠ΅ΠΌΡ, ΠΈΡΠΏΠΎΠ»ΡΠ·ΡΡ iCloud/Google, ΠΏΡΠΈΡΠ»Π°ΡΡ ΠΊΠΎΠ΄/ΠΏΠ°ΡΠΎΠ»Ρ, Π·Π°ΠΏΡΡΡΠΈΡΡ ΠΊΠΎΠ΄/ΠΠ, Π½Π΅ Π΄Π΅Π»Π°ΠΉΡΠ΅ ΡΡΠΎΠ³ΠΎ - ΡΡΠΎ ΠΌΠΎΡΠ΅Π½Π½ΠΈΠΊΠΈ. ΠΠ±ΡΠ·Π°ΡΠ΅Π»ΡΠ½ΠΎ ΠΆΠΌΠΈΡΠ΅ "ΠΠΎΠΆΠ°Π»ΠΎΠ²Π°ΡΡΡΡ" ΠΈΠ»ΠΈ ΠΏΠΈΡΠΈΡΠ΅ Π² ΠΏΠΎΠ΄Π΄Π΅ΡΠΆΠΊΡ. ΠΠΎΠ΄ΡΠΎΠ±Π½Π΅Π΅ Π² Π³Π°ΠΉΠ΄Π΅ β
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