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4 часа Π½Π°Π·Π°Π΄

Sr Electrical Engineer (Medical Devices)

Π’ΠΈΠΏ Ρ€Π°Π±ΠΎΡ‚Ρ‹
fulltime
Π“Ρ€Π΅ΠΉΠ΄
senior
Английский
b2
Π‘Ρ‚Ρ€Π°Π½Π°
US
Вакансия ΠΈΠ· списка Hirify.GlobalВакансия ΠΈΠ· Hirify Global, списка ΠΌΠ΅ΠΆΠ΄ΡƒΠ½Π°Ρ€ΠΎΠ΄Π½Ρ‹Ρ… tech-ΠΊΠΎΠΌΠΏΠ°Π½ΠΈΠΉ
Для мэтча ΠΈ ΠΎΡ‚ΠΊΠ»ΠΈΠΊΠ° Π½ΡƒΠΆΠ΅Π½ Plus

ΠœΡΡ‚Ρ‡ & Π‘ΠΎΠΏΡ€ΠΎΠ²ΠΎΠ΄

Для мэтча с этой вакансиСй Π½ΡƒΠΆΠ΅Π½ Plus

ОписаниС вакансии

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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

hirify.global 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

  • Bachelor’s degree with 8 years, Master’s 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.

Π‘ΡƒΠ΄ΡŒΡ‚Π΅ остороТны: Ссли Ρ€Π°Π±ΠΎΡ‚ΠΎΠ΄Π°Ρ‚Π΅Π»ΡŒ просит Π²ΠΎΠΉΡ‚ΠΈ Π² ΠΈΡ… систСму, ΠΈΡΠΏΠΎΠ»ΡŒΠ·ΡƒΡ iCloud/Google, ΠΏΡ€ΠΈΡΠ»Π°Ρ‚ΡŒ ΠΊΠΎΠ΄/ΠΏΠ°Ρ€ΠΎΠ»ΡŒ, Π·Π°ΠΏΡƒΡΡ‚ΠΈΡ‚ΡŒ ΠΊΠΎΠ΄/ПО, Π½Π΅ Π΄Π΅Π»Π°ΠΉΡ‚Π΅ этого - это мошСнники. ΠžΠ±ΡΠ·Π°Ρ‚Π΅Π»ΡŒΠ½ΠΎ ΠΆΠΌΠΈΡ‚Π΅ "ΠŸΠΎΠΆΠ°Π»ΠΎΠ²Π°Ρ‚ΡŒΡΡ" ΠΈΠ»ΠΈ ΠΏΠΈΡˆΠΈΡ‚Π΅ Π² ΠΏΠΎΠ΄Π΄Π΅Ρ€ΠΆΠΊΡƒ. ΠŸΠΎΠ΄Ρ€ΠΎΠ±Π½Π΅Π΅ Π² Π³Π°ΠΉΠ΄Π΅ β†’