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Who are we?
German company specialised in international regulatory affairs for medical devices and in vitro diagnostics. The spirit of partnership is important to us – not only in our relationships with our clients and partners but also in the relationships among the individuals who work for CEplus. Our business culture is based on open communication and on a structure that accommodates each individual’s knowledge and skills. As an ambitious and progressive independent Regulatory Affairs service provider, we offer the opportunity for an IVD expert to join our team based in Southern Germany near Basel.
What we offer:
As a regulatory affairs expert (m/f/d) on in-vitro diagnostic (IVD) medical devices you will focus on the regulatory support of IVD and companion diagnostic (CDx) products throughout the entire product lifecycle. You will have the opportunity to work on a variety of different projects within our CEplus team and you will be involved in various tasks, such as:
Are you interested?
This is full time job, which is done partly on-site and partly from remote location.
If you possess above mentioned skills please send your application including cover letter, curriculum vitae and references to our human resources team at firstname.lastname@example.org
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