Regulatory Affairs Manager

Your main task is to ensure compliance with the regulatory requirements for several countries with focus on Asia. This includes the development and maintenance of regulatory documentation as well as participation in international product approval. For this you will work closely with internal departments, dealers and distributors as well as representatives of the parent DENTSPLY. Check product labels and instructions for use and release this. Rounding out the task by the pursuit of legal and normative development in medical devices.

You have your degree in Science or in technical areas such as medical completed successfully and have a good knowledge of the legal and regulatory requirements for the medical device industry (eg MPG). You feature a careful, responsible operation, and in a concise manner of expression in speech and writing. Good knowledge of standard MS Office applications and excellent knowledge of English and writing complete your profile.