Regulatory Affairs Specialist in Utrecht
Your position as a Regulatory Affairs Specialist is in our Quality Management team where we always have various projects on the agenda. Regulatory affairs for medical devices is a wide area with a wide range of expertise in clinical and in technical aspects.
Your main responsibilities consists of:
You are looking for the next step in your career and looking to work in a dynamic international team where you further build up your career in the regulatory environment. Next to that you are a talented professional with preferably toxicological experience.
Education & Experience