Regulatory Affairs - Medtech/Software - Stockholm

Keen on working in a smaller firm that listens to your needs and try to work around? Do you like working closely, yet with a lot of autonomy with a variety of clients? I am right now recruiting for a medical device consultancy firm in Stockholm that is offering exactly this opportunity.

I am looking for regulatory affairs person within medical devices with work experience regarding IEC 62304, risk management and usability. We ideally see that you have 3-5 years experience in total and can be based out of Stockholm.

My client is a consultancy firm focused on quality assurance and regulatory affairs with a specific focus on small to mid-size companies. You will work closely with these clients and play a large part in driving the process forward and finding the best solutions together with them. The focus in this role in particular is on medical device software.

Whilst being a consultant obviously means you need to have a lot of commitment, my client also tries to accommodate your situation as much as possible. For example, you can work partly from home if necessary and you have a say in which clients you get to work for, meaning this company actually really cares about your personal life, as well as professional development.

Get in touch with Anders Sandberg at NonStop Recruitment by sending your CV to a.sandberg@nonstop-pharma.com.

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for full list of the niche markets we cover.