Medical Device Test Engineer: Hardware & QA in Brownhills

Medical Device Test Engineer: Hardware & QA in Brownhills

Brownhills Full-Time 29700 - 36300 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Validate medical devices through hands-on testing and ensure quality compliance.
  • Company: Xstrahl Ltd, a leader in medical technology innovation.
  • Benefits: Competitive salary and exciting growth opportunities in your career.
  • Why this job: Make a difference in healthcare by ensuring the quality of life-saving devices.
  • Qualifications: Experience in hardware testing and knowledge of quality management systems.

The predicted salary is between 29700 - 36300 Β£ per year.

Xstrahl Ltd in Brownhills, Walsall, UK, is seeking a Test Engineer to validate our medical therapy and research cabinets. You will execute test scripts and procedures across mechanical, electromechanical and electronic hardware, ensuring quality and compliance.

Required is hands-on hardware testing experience, familiarity with quality management systems, and ability to document results for regulatory submissions. This role offers a competitive salary and growth opportunities.

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Medical Device Test Engineer: Hardware & QA in Brownhills employer: KaneHR

At KaneHR, we pride ourselves on being a dynamic and supportive consultancy that values the growth and development of our employees. As an HR Advisor, you'll enjoy a diverse range of experiences while working closely with ambitious organisations that prioritise their people and culture. With a focus on professional development and meaningful client relationships, this role offers a unique opportunity to make a real impact in a collaborative environment.

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Contact Details:

KaneHR Recruitment Team

We think you need these skills to ace Medical Device Test Engineer: Hardware & QA in Brownhills

Hands-on Hardware Testing Experience
Familiarity with Quality Management Systems
Test Script Execution
Mechanical Testing
Electromechanical Testing
Electronic Hardware Testing
Documentation for Regulatory Submissions