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For our Life Science team, we are looking for an experienced quality assurance engineer who are passionate about quality assurance for medical devices and thrives among development engineers.
Do you want to work in a consulting and development house where new technology is in focus? Will you help us keeping focus on quality compliance?
You will work with quality management systems for medical devices. Your tasks could be helping a start-up company setting up their 13485 compliant QMS or it could be assisting established medical device development company with updating and improving their QMS.
As our new colleague, it is important that you:
As a person, you have a passion for quality, and have a strong personal drive yet you are open minded and pragmatic. You collaborate and communicate well with others and you will use these skills to help us expand this area of competence.
For us development is a natural part of all aspects of life – from idea to product and from career to personal life. At Prevas there is room for you, for your ideas, and for your view of the world.
Passion and creativity are reflected in our projects. Our energy spread to our collaboration and social interactions both in and outside office hours. We host several yearly social events with and without families. We also have Friday-afternoon-bar, excursions, hobby club and lots more.
We are embedded in our DNA and we are focused on being the preferred provider of embedded development to our customers. We often work very closely with our customers, and as Prevas employee, you will often come into close contact with many different customers’ development departments, either as project member at our office in Herlev, or on-site in the customer’s development team.
Are you interested in the job send your application and CV via the form below. We call for interviews on an ongoing basis.