Beschreibung
SENOVO IT is urgently looking for a Regulatory Affairs Consultant to start a mission immediately.
The job spec can be found below:
Strong working knowledge of EU Medical Device Regulations and guidance documents as well as relevant standards.
Ability to work with cross-functional team members including (but not limited to) R&D, Quality, Labeling, Sterility, Medical and Clinical.
Experience in working with PLM systems (ie Agile and Windchill).
Strong proficiency in Microsoft Office including Word and Excel.
Excellent written and oral communication skills.
Languages: English required, German a plus.
Ability to manage multiple tasks and be detail-oriented.
RAC certification is a strong preference
If interested in this opportunity please apply immediately, it is an English speaking project, knowledge of German is advantageous.