Назад
Company hidden
15 часов назад

Principal Systems Engineer (MedTech)

170 000 - 190 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Principal Systems Engineer (MedTech): Defining system-level requirements and architectures for regulated cardiac medical devices with an accent on patient needs, cross-functional engineering coordination, and product risk management. Focus on translating market requirements into detailed engineering specifications, leading technical investigations, and supporting verification, reliability testing, FMECA analysis, and design validation.

Location: Pittsburgh, PA, United States; onsite at hirify.global offices

Annual salary: $170,000–$190,000

Company

hirify.global develops cardiac medical devices, software, and related services, including wearable defibrillators, heart failure monitoring systems, and oxygen therapy products.

What you will do

  • Collaborate with product management, medical affairs, regulatory affairs, and human factors teams to identify and prioritize patient and stakeholder needs.
  • Translate market requirements and user needs into system-level and detailed engineering requirements.
  • Lead system architecture definition and collaborate with engineering teams to refine the architecture.
  • Drive technical investigations addressing architectural uncertainties, requirement gaps, and technical risks.
  • Support test case generation, engineering verification, reliability testing, FMECA analysis, and product risk management.
  • Coordinate major activities across the multifunctional engineering team throughout the product development lifecycle and help identify resource needs.

Requirements

  • Bachelor’s or master’s degree, or equivalent industry experience, in engineering or a related discipline.
  • At least 10 years of product development experience.
  • Proven experience leading engineering research and development activities.
  • Strong analytical, decision-making, conflict-resolution, verbal, and written communication skills.
  • Ability to work onsite at the Pittsburgh, PA offices.

Nice to have

  • 15 or more years of industry experience with FDA-regulated medical devices.

Culture & Benefits

  • Work on technologies intended to improve outcomes for patients with serious cardiopulmonary and respiratory conditions.
  • Work in a fast-growing company operating in more than 140 countries.
  • Culture emphasizing innovation, self-motivation, and an entrepreneurial spirit.
  • Evening and weekend work may occasionally be required.
  • Comprehensive benefits plans are available.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →