Career at QAdvis

Quality & Regulatory consultant

QAdvis AB is based in Sweden with two offices. We are expert consultants supporting clients worldwide, with an emphasis on Scandinavian and European companies.

Who are we looking for

To our offices in Lund and Stockholm we are now looking for new colleagues that will work together with us and our clients as Quality & Regulatory consultant within the Medical Device and In Vitro Diagnostic medical device industry.

As a consultant at QAdvis

You will work together with a fantastic team and support our clients with qualified QA and RA advice and hands-on work. Activities span over several areas and your personality and competence will be matched with our company and client’s needs.

Following skills

We expect that you are a positive, curious, solutions-oriented and service minded person. You have good knowledge about the regulatory frameworks and quality management systems for medical devices and/or in-vitro diagnostic devices. You also have excellent skills in English and Swedish. Other languages are appreciated as we have clients in different markets. Your basic education could be clinical, engineering, law, science or similar.

Welcome with your application!

When you send your CV and application to QAdvis you agree to that we handle and keep the records with your personal information. We will keep your CV-records for 6 month.

Lund area

Annelie Hagström
annelie.hagstrom@qadvis.com
+46 73 541 31 46

Stockholm area

Emma Axelsson
emma.axelsson@qadvis.com
+46 707 964 141

Spontaneous
application

jobs@qadvis.com