Regulatory Affairs Manager - Tuttlingen (M/F) Medical Devices

The Role:

* Regulatory requirements for global approvals

* Liaison with appropriate Regulatory authorities

* Maintaining the requirements in the development process

* Specific training in the development of normative aspects

* Changes to the approvals, standards and the effect they will have on products

* Contact for both national and global teams

Your Profile:

* 2+ Years experience work experience within the area of Regulatory Affairs

* Completed studies in an appropriate area

* Knowledge in the area of Regulatory Submissions for Medical Devices

* Over C1 Level in both German and English

If you are or know anyone that would be interested in this amazing opportunity at a Medical Device company with a huge global presence, please either respond with your interest to this Job Ad, or alternatively directly send your application to d.perkins@sciproglobal.de