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7 часов назад

Junior Test Engineer (Medical Devices)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
Germany
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR

Junior Test Engineer (Medical Devices): Supporting the testing and verification of medical devices and tubing sets with an accent on system tests, hardware/software validation, and regulatory compliance. Focus on building and validating test stations, executing functional and regression tests, and ensuring adherence to ISO 13485 and FDA standards.

Location: Onsite in Berlin, Germany

Company

Global innovator providing extreme precision components and sub-systems for healthcare and advanced manufacturing.

What you will do

  • Prepare and execute test specifications for system and component tests (Level 2 and 3).
  • Build and validate hardware and software test stations for medical production, including sensor technology.
  • Conduct functional, performance, and regression testing to ensure product quality and safety.
  • Collaborate with design engineers and production teams to identify, document, and track defects.
  • Maintain detailed documentation for testing procedures and reports to ensure version control and traceability.
  • Perform calibration and routine maintenance of testing equipment to ensure reliable results.

Requirements

  • Bachelor's degree in Electrical Engineering, Biomedical Engineering, Mechatronics, or a related technical field.
  • Foundational understanding of test execution and test case design.
  • Strong analytical skills for root cause analysis and defect identification.
  • Ability to maintain meticulous documentation and records.
  • Strong teamwork and communication skills for cross-functional collaboration.
  • Location: Must be based in or able to work onsite in Berlin, Germany.

Nice to have

  • Basic programming or scripting knowledge (e.g., Python, C#) and interest in test automation.
  • Basic awareness of medical device regulatory standards such as ISO 13485 and FDA regulations.
  • Previous internships, working-student roles, or academic projects in QA, electronics, or software development.

Culture & Benefits

  • Collaborative global team environment across 26+ offices.
  • Culture that embraces teamwork, collaboration, and empowerment.
  • Opportunity to work on mission-critical technology improving healthcare and productivity.
  • Guided professional growth within a highly regulated medical device environment.

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