We are looking for a 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.
Experience from regulatory affairs is expected, and if you are up to speed with the new regulatory frameworks MDR and Biocid, is a great advantage.
The position is based in Stockholm, but the Company is operating on the global market. English is the business language.
If you would like to learn more about this position, please contact Ulrika Nyberg at +46 708 80 04 07 or email@example.com