Become part of our team!

Do you have extensive knowledge and experience of regulatory affairs within development of medical device? Would you like a key role in supporting innovative companies with regulatory strategies and hands-on operations? That’s a Senior Consultant at SDS MedteQ!

SDS MedteQ is a privately owned consultancy company. Together with our sister company, SDS Life Science, we are a leading Nordic company supporting clients with regulatory guidance, quality assurance, design of clinical study programs and development of medical device, pharmaceuticals, and combination products. We truly believe in work-life balance, a supportive culture and continuous professional growth. We are proud to be certified a “Great Place to Work”.

As a consultancy, we match your competence to the needs of our clients as much as possible. Here are some examples of assignments we have worked with: 

  • Classification of novel products. Is it a medical device? What class? A combination product or something else?
  • Creating feasible strategies from early development stages to commercialization, from a regulatory perspective
  • Selecting and managing contact with notified bodies 
  • Communication with authorities, mainly EU and FDA, and interpretation of regulations, standards & guidelines. 

Read more and apply for the job below. Our friends at Search4S helps us with the recruitment. 

Read more and apply

We use cookies to ensure that we give you the best experience on our website. Read our cookie policy here.