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Consultant Medical Devices Regulatory

Germany, Baden-Württemberg, StuttgartMedical Devices

Job description

What you'll do
Currently, Qserve has an exciting opportunity to join our team as a Senior Consultant Regulatory. As a Qserve consultant, you serve a wide variety of clients in the medical device industry. With your regulatory knowledge of medical devices, you will be responsible for helping Qserve clients facilitate their business goals by (hands-on) help, assuring regulatory compliance, and market access for a wide range of medical devices. You will be part of a team of medical device experts, working from across the world, dedicated to supporting our clients.

Job requirements

What you’ll bring to the team

The candidate we are looking for is a highly motivated and passionate Senior Regulatory professional, who has experience in writing and reviewing technical documentation of medical devices. With your understanding of design and development processes (specifications, verification, and validation) and risk analysis you are able to engage a large variety of medical device technologies and guide clients to successful global compliance. In this role, you thrive on variety and be able to manage multiple projects. You enjoy teaching and coaching and are able to effectively communicate regulatory subjects to both technical and non-technical people. We are a service-oriented organization so you must thrive on helping others. You like to write technical documentation and regulatory documents.

Your profile:

  • Technical or scientific degree (BSc, MSc, or Ph.D.) in physics, mechanical engineering, chemistry, (medical) biology, biomedical technology, or similar;
  • At least 7 years of working experience in the field of medical devices (EU-MDD and EU-MDR) through positions in industry, consultancy, or Notified Body, in either quality, regulatory or clinical roles (e.g. Manager Regulatory Affairs & Quality Assurance);
  • Knowledge of Medical Device Regulations (EU MDR, FDA, PAL, TGA, etc.);
  • Direct experience with writing technical documentation and regulatory documents;
  • Experience with Medical device Quality management systems / ISO 13485;
  • Pragmatic, enjoying a mix of activities in regulatory affairs or quality assurance;
  • Communicative and service-oriented;
  • Strong organizational skills, detail-oriented to deal with various projects at the same time;
  • Fluent in English.


Getting excited about a career in the dynamic and innovating world of medical devices? Then please submit your resume and motivation!


How we hire

Everything you need to know about your application process at Qserve Group

Getting to know you

In the first call, let our recruiter learn about you and your story to check a potential fit for Qserve. This is also a chance for you to ask first questions about the role and company.


In this meeting, your future manager takes a deeper dive into your experience and what you could bring to the team. Expect questions on how knowledgeable you are in your area of expertise.

Final chat

You made it to the very last stage! Here we have a final call to ask some additional questions. This meeting will be between you, your future manager and a team member.

Mutual interest

Is there a match? Then we will gladly make you an offer consisting of a suitable salary and our employment conditions. Do you accept our offer? Your adventure at Qserve Group will start!