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3 дня назад

System Engineer II (MedTech)

91 200 - 114 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR

System Engineer II (MedTech): Developing and improving test solutions for wearable medical devices and manufacturing systems with an accent on automated test processes and product reliability. Focus on designing test fixtures, analyzing test data using statistical tools, and ensuring compliance with medical device regulatory standards.

Location: Hybrid in San Francisco, CA (minimum 50% in-office presence). Must be legally authorized to work in the United States; sponsorship is not available.

Salary: $91,200 - $114,000

Company

hirify.global is a leading digital healthcare company specializing in wearable biosensors and cloud-based analytics to detect, predict, and prevent cardiac disease.

What you will do

  • Design and improve test fixtures and systems in collaboration with R&D and manufacturing teams.
  • Develop automated test processes and procedures to support verification and validation.
  • Create and maintain technical documentation, including Test Plans, System Requirements, and Test Reports.
  • Analyze test data and verify capability using statistical tools such as GR&R studies.
  • Utilize bench-top equipment like power supplies, DMMs, and oscilloscopes for system evaluation and debugging.
  • Ensure all work complies with medical device regulatory standards and internal quality procedures.

Requirements

  • Bachelor’s degree in Electrical Engineering, Biomedical Engineering, or a related field.
  • 3–5 years of relevant experience in system test, manufacturing test, or product development.
  • Proficiency in Python or C# for test automation and data analysis.
  • Strong understanding of test instrumentation and measurement principles.
  • Must be legally authorized to work in the US on an ongoing basis without sponsorship.

Nice to have

  • Experience with electromechanical or wearable medical devices.
  • Prior work in a regulated manufacturing or medical device environment.
  • Familiarity with ISO 13485, FDA 21 CFR Part 820, or similar quality system standards.
  • Experience with design of experiments (DOE), statistical analysis, or measurement system analysis (MSA).

Culture & Benefits

  • Mission-driven environment focused on impacting global cardiac health and patient outcomes.
  • Dynamic workplace that values innovation, collaboration, and rapid professional growth.
  • Competitive benefits package.
  • Inclusive culture that welcomes diverse backgrounds, experiences, and perspectives.

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