Senior Regulatory Affairs Consultant

Become part of our team!

Do you want to help companies at the forefront of technology get products into all different markets? We’re hiring a regulatory affairs consultant with a thorough understanding of the regulatory processes in medical technology. As a consultant at SDS MedteQ, you work on exciting and developing projects from a knowledge base with competent senior colleagues.

The demand for our services is high. Therefore, as a consultant, you have great opportunities to influence the type of assignment you work with and how you do it. We usually work together with the client as a team.  


Examples of assignments

  • Classification of a completely new product, both medical technology and/or combination or borderline product
  • Define regulatory strategies from early development to CE-marking and commercialization
  • On behalf of the customer, interact with the notified body and/or competent authorities.
  • Interpretation and implementation of regulations, standards, and guidelines

Qualification requirements

You have worked for several years with regulatory issues in medical technology. As a senior consultant, we expect that you run your regulatory projects independently. But, of course, we will help when needed. It is also important that you find it exciting to take on new projects for different products and customers. At the same time, you value collaboration and communication.

Does it sound like you? Please send us your application as soon as possible. 


Stockholm, Lund, or Uppsala. Remote work is up negotiable. 


Permanent employment with SDS MedteQ as the employer. Full or part-time.

Start date

Flexible, by agreement

Application and contact

Send CV and cover letter to Johan Sköld at

NOTE: We are interviewing continuously, so don't wait to apply.


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