Join us and become part of our international Regulatory Affairs Team at our Headquarter in Basel. We are looking for you as international Regulatory Affairs Manager.
In this role, you are responsible for the registration of Straumann products in international markets. You plan the registration strategies and coordination, implementation, execution control and completion of product registration, assuring compliance with regulatory requirements.
International Regulatory Affairs Manager (m/f)
Registration of new products in assigned countries
Product lifecycle management and product license maintenance
Set up registration strategies, execute registration process from dossiers
compiling to submissions and approvals of assigned products throughout various
Be the point of contact for Regulatory Affairs related matters to the assigned
countries University degree in a scientific discipline such as biology, pharmacy,
chemistry, engineering or equivalent
Minimum 3 years overall Medical Device Regulatory Affairs experience with a
track record in international registrations
Experience in directly and/or indirectly, and successfully interacting with
Health Authorities and other regulatory bodies
Experience in obtaining fast approvals of high risk class Medical Devices,
preferably in dental implantsExcellent command of spoken and written English
Distinct communicative and professional, independent and team oriented work
behavior We offer...
A creative, inspired and engaged team on a mission: #WeRockDentistry
The ability to take ownership for your solution field as an expert
The chance to create your footprint in the dental industry
An informal, hands-on working environment with opportunities to grow - it's fun
to work with us
Institut Straumann AG