|Publication date:||August 31 2020|
For a rapidly growing scale-up active in the medical devices industry, we are looking for a QA Engineer with experience within the medical devices industry (ISO:13485). The organisation develops and produces innovative and life changing electronic medical devices with the goal to give people more time to enjoy life, and they want to be a company where people can rely on. Currently, the organisation experiences tremendous growth, and is expected to become a global leader in the near future. At the moment, about 100 employees work at the organisation, which mainly consist of talented and ambitious professionals who believe in a work hard/play hard approach. You will be part of the quality department which now consists of 15 employees and report directly to the Senior Regulatory Affairs Manager.
Within this role as QA Engineer, you will have a focus on implementing and working with the guidelines of the MDR. As an example, you will update and prepare technical documentation. The organisation is known for their innovative product, and therefore it is essential that complaints are handled correctly, but also data and trend analysis are of key importance in order to improve and optimise current processes. Next to that, you will work in a team of three people to analyse and discover post market trends of the product and work on risk management to assist in determining failure mode.
The organisation is looking for someone who, ideally, has the following profile:
The organisation can offer you the following:
If you are interested in this job, or in similar ones, please feel free to contact me directly.
Associate Medical Devices