Verification & Validation Engineer

Location

Mölnlycke

Apply by

2023-03-30

When you can´t breathe, nothing else matters

Our vision at Breas is to provide innovative solutions that enable people with chronic respiratory conditions to live life to the fullest.

Are you a Verification & Validation Engineer, who wants to make an impact and change the world of ventilation for the better? Then we have the place for you.

At Breas Medical you will have the chance to work on projects of high importance that improves the quality of life of our end users. Working at Breas Medical will be a new impactful chapter of your life and be a great opportunity for growth. You will be joining Breas at a very exciting stage of our journey with a broad product portfolio as well as new products to manage. Our products enable us in our aim to be the preferred choice of our customers and the global market leader within the mechanical ventilator product segment.

This position is based at R&D at the Breas global headquarter in Mölnlycke, Sweden. Breas Medical is owned by Fosun Pharmaceutical (Group).

About the role

As Verification & Validation Engineer you will make sure that products work as intended and without problems.

Breas develops and produces medical devices that helps patients to breathe. Some of Breas products are life supporting. It is very important that the products are safe to use and thoroughly tested. The Verification & Validation Engineer fills an important role in making sure that is the case.

You will be responsible for planning and performing verification activities together with the R&D and Marketing teams. You will work in projects for development of new products as well as with updates of existing products.

What will you do

  • Coordinate, perform and report Verification & Validation of product design
  • Develop test methods
  • Work with a variety of test equipment for measuring performance and functions of Breas products
  • Work together with the R&D team to decide test methods and tools for Verification & Validation
  • Handle documentation of test cases and reports
  • Raise defects in product design

Your background & experiences

  • Academic background in Engineering (Bachelor or Master’s degree) or corresponding experience
  • Knowledge of the medical device industry and relevant standards (e.g. ISO 13485, IEC 60601, MDR) is considered a merit
  • Experience working with test labs (NRTLs) is considered a merit
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