Senior Regulatory Affairs Specialist, Medtech, Stockholm 

We are looking for a Senior Regulatory Affairs Associate to a Medtech company in Stockholm.

Purpose of the Position is to obtain and maintain marketing authorizations for the company’s products worldwide and ensuring compliance with laws and regulations set by the Healthcare Products & Regulatory Agencies. 

The Position will also support regulatory strategy, guidance to organization on regulatory affairs matters throughout the life cycle of a medical device from product development, placing product on market and ongoing commercial supply and product maintenance.


We are looking for a team-player and a doer and a skilled collaborator with a positive mindset and is continuously motivated and curious. You have drive and motivation and you are meticulous. In this role, the details are important.

We expect you to have strong experience from regulatory affairs and the new regulatory frameworks MDR and Biocid. 


The position is based in Stockholm, but the Company is operating on the global market. English is the business language. 

If this position attracts you, please apply by sending a CV and application via the link here!


Ulrika Nyberg,, +46708800407

Ulrika Nyberg

Telefonnummer: +46 (0) 708 800 407