|Employee Regulatory Affairs (m/f/d) for the implementation of Medical Device Regulation.

We are a company working for an American premium manufacturer in the medical sector as a sales and service organization and are looking for your know-how to strengthen us with immediate effect.

Your field of activity:

• Coordinate internal and external projects for the implementation of MDR 2017/745.
• You are the internal contact person as well as for business partners for questions regarding the fulfilment of regulatory requirements in the medical device environment.
• Communication with business partners regarding the implementation of MDR 2017/745.

Your qualifications:

• Initial experience in the field of regulatory affairs and approvals of medical devices (including MDR 2017/745 and ISO 13485).
• High degree of diligence and reliability
• Communication skills
• Self-organised
• Fluent in written and spoken German and English

Please send your application to: karriere@tecserena.com

or in writing to:
Tecserena GmbH
Maternusstr. 44
50996 Köln