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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
Mediq is een belangrijke speler in de internationale zorg. Iedere dag verbeteren we de kwaliteit van leven van miljoenen mensen. We leveren medische hulpmiddelen en zorgoplossingen. Thuis, via huisartsen, in ziekenhuizen of andere zorginstellingen.
We komen graag in gesprek met professionals die zich aangesproken voelen door de maatschappelijke relevantie van de zorgsector. Enthousiastelingen met een ondernemende, initiatiefrijke instelling.
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