Join us and become part of our Corporate Quality Management & Regulatory Affairs Team at our Headquarter in Basel. We are looking for you as Regulatory Affairs Manager
In your role, you will be responsible for the overall product registration strategies, coordination, implementation, execution, control and completion of product registrations mainly in EMEA for our brands. The role is based at our Headquarters in Basel.
Regulatory Affairs Manager EMEA / APAC / Emerging Markets (m/f)
Preparing technical files for international registrations
Registration of the products in EMEA and APAC market
Product lifecycle management and product license maintenance
Set up registration strategies; execute registration process from dossier
compiling to submission and approvals of assigned products throughout various
regions MSc or BSc in Life Science (biology, pharmacy, chemistry, or equivalent)
5 years' experience in General Regulatory Affairs, with at least 2 years of
international regulatory experience
Hands-On experience with international medical device (class II & III)
regulatory approvals and submissions is a must.
Experience in directly and/or indirectly, and successfully interacting with
Health Authorities and other regulatory bodies
Agility to handle and deliver on a multitude of projects, programs, and
priorities paired with high sense for execution and teamwork 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.
Marcus Fischer, Head of Global Talent Acquisition, is your first contact for
further questions you might have.
Please apply via our online application system and do not send your application
For this position, we are not asking for profiles of HR Consultancies and
Recruiting Agents. Please respect this.
Institut Straumann AG