test automationasicelectrical engineeringfirmwarerfpcb designemcemimedical devicesmixed signal electronicsmedical device design controls
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$171к-257к/год
$170к$200кмедиана$230к
По похожим ролям (49) ~ $200к/год
На СНГ рынке: $4.5к/мес ($4.2к - $5.9к)
90
Крутая вакансия
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Чётко очерченная руководящая роль в крупной медицинской технологической компании: команда опытных инженеров и критически важные для безопасности продукты. Главный компромисс - обязательная работа в офисе пять дней в неделю.
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Офис каждый деньПонятная зона ответственностиЗаметный вклад в здоровьеШирокий пакет льгот
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Sr. Electrical Engineering Manager (CRM) (Medical Devices): Leading a 10–15-person electrical system design team developing high-reliability, safety-critical electronics for implantable cardiac devices and external systems with an accent on PCB design, mixed-signal electronics, RF/telemetry, firmware and ASIC integration, and medical device compliance. Focus on defining functional strategy, balancing product-program delivery with capability development, resolving complex hardware and manufacturing issues, and ensuring rigorous verification, design transfer, and post-market support.
Location: Mounds View, Minnesota, United States; onsite at least 5 days per week.
Salary: $171,200–$256,800 per year.
Company
hirify.global develops healthcare technologies, including cardiac rhythm management therapies and medical devices.
What you will do
Define and advance the Electrical System Design functional strategy, engineering methods, tools, and capability investments.
Lead a team of 10–15 engineers across multiple product platforms and concurrent development programs.
Plan resources, prioritize commitments, and align engineering execution with program cost, scope, schedule, and business priorities.
Ensure robust electrical and PCB designs, requirements, documentation, characterization, verification, and compliance with medical device design controls.
Lead integration across PCB hardware, ASICs, firmware, mechanical interfaces, sensors, and telemetry/RF systems.
Guide root-cause analysis, technical tradeoffs, production test readiness, design transfer, yield improvement, sustaining support, and continuous improvement.
Requirements
Bachelor’s degree in Electrical Engineering, Computer Engineering, Biomedical Engineering, or a related technical field.
At least 7 years of relevant technical experience and 5+ years of managerial or people leadership experience; or an advanced degree with at least 5 years of relevant technical experience and 5+ years of managerial or people leadership experience.
Experience leading electrical engineering, product engineering, hardware integration, or systems integration teams in a regulated product development environment.
Technical breadth across PCB design, analog and mixed-signal electronics, digital interfaces, RF/telemetry, ultra-low-power design, EMI/EMC, manufacturing test, and product integration.
Experience with medical device design controls, verification and validation, requirements management, risk management, and post-market support.
Experience integrating PCB hardware with firmware, ASICs, mechanical systems, sensors, electrodes, batteries, telemetry systems, or other embedded technologies.
Ability to lead root-cause investigations, resolve complex system-level interactions, make technical and business tradeoffs, influence stakeholders, and drive cross-functional alignment.
Strong communication, leadership, documentation, interpersonal, talent development, and team-building skills.
For baccalaureate degrees earned outside the United States, the degree must satisfy 8 C.F.R. § 214.2(h)(4)(iii)(A).
Roles below Principal level require unrestricted U.S. work authorization at the time of hire and throughout employment.
Nice to have
Experience developing Class III medical devices, active implantable medical devices, or other high-reliability safety-critical products.
Experience with MRI safety, electromagnetic compatibility, implantable device reliability, ISO 14708, IEC 60601, or other relevant medical device standards.
Experience partnering with global manufacturing sites, suppliers, technical sourcing, operations, quality, reliability, regulatory, and program management.
Experience developing technical talent and building an inclusive, accountable, high-performing engineering culture.
Culture & Benefits
In-person collaboration and professional growth in an onsite environment.
Health, dental, vision, life, disability, and retirement benefits for eligible regular employees.
Paid time off, paid holidays, employee assistance, tuition assistance, and healthcare or dependent-care spending accounts.
Short-term incentive eligibility through the hirify.global Incentive Plan and access to employee stock purchase benefits.
Work is performed under applicable internal procedures, regulatory expectations, and external medical device standards.
Hiring process
Ensure the resume clearly demonstrates the stated minimum education, technical experience, and people leadership requirements.
Apply only through official hirify.global channels; legitimate recruiting communications use approved hirify.global platforms and official @hirify.global.com addresses.
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