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:
What is your background?
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
The sourcing team enables Mediq to outperform competition by growth, profitability and value creation via the external supply base. It is a strategic function that leverages the scale of Mediq, drives tangible impact to the bottom line and enables new revenue streams via innovation and commercial partnerships. We continuously benchmark the internal organization against external best practices and mobilize the organization for change. And lead all commercial supplier communication and are committed to fair awarding, compliance and to tangible cost improvements.
Apply now if you're interested in this vacancy! Make sure you have the following documents ready to add to your application.