Regulatory Affairs Liaison M/F/D

Job description

Job Description Do you want to be part of our Regulatory Affairs Europe team, supporting accessibility to our new and already registered medicines? We have a new, exciting opportunity for a Regulatory Affairs Liaison to be based in Oss (NL), Brussels (BE), or London (UK). Purpose of the position: In this role, you will have the opportunity to coordinate regulatory activities in the EU, UK, Switzerland, and non-EU SEE countries under the supervision of the (Senior) Principal Scientist of Regulatory Affairs. You will be responsible for implementing strategies for products in development with their guidance and independently developing and executing strategies for registered products. Additionally, you will play a crucial role in managing submissions and interactions with the EU regulatory agencies. It will be your responsibility to directly liaise with HQ US-based cross-functional teams, effectively communicating regional requirements and ensuring compliance with all necessary regulations for assigned projects. You will also coordinate or oversee the preparation of regulatory documentation in a timely manner, aligning with corporate objectives. Furthermore, as an integral part of the...