Senior Regulatory Consultant

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. 

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