Verification Engineer



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Breas Medical was founded in 1991 in Gothenburg, Sweden, Breas Medical has become one of the global leaders in Home Mechanical Ventilation, Airway Clearance and Sleep therapy. Our vision is to provide Better breathing and quality of life to respiratory patients around the world and to help patients transition from Hospital to Home. Breas is headquartered in Sweden and has subsidiaries in the UK, Germany, Spain, USA and China. Together with network of highly specialized distributors, we serve over 40 countries worldwide. The Breas brands Vivo, Nippy, Clearway and Z1 are widely recognized and appreciated for their performance, ease of use and attractive design. Breas has approximately 200 employees, 70 of which in the USA.
Our focus is first and foremost on the patients and customers we serve. We highly value our relationships, never compromise on quality, continuously improve customer support, and expand our clinical excellence program consisting of study days, webinars, educational videos, symposia and clinical research. We work closely together with key opinion leaders around the world to stay updated on the latest clinical insights.

Breas Medical provides a full line of innovative respiratory medical devices to our patients. As we are embracing another stage of fast expansion, we are looking for a Verification Engineer to join our forward-thinking team. The successful candidate will be a member of the R/D team  to support existing product improvements and new product transfer at Breas Medical’s facility in Billerica, MA. We provide the tools and time to learn, make mistakes, and grow with us!


  • Perform testing and documentation on the various different respiratory devices which Breas Medical AB is preparing to release as sellable products for patient use.
  • Write test protocols to verify that they meet the product design and performance requirements
  • Test protocols to verify that they meet the product design and performance requirements
  • Investigate issues which arise based on the product not being able to meet design and performance requirements.
  • Collect data and document test results.


  • B.S. or M.S. degree in engineering discipline
  • Solid foundation in engineering and scientific fundamentals
  • 6 months to 1 year of experience in assisting product development efforts involving verification and validation in the medical device industry.



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