The Company

Our client is a leading biopharmaceutical company engaged in the discovery and development of innovative medical solutions. This company produces medicines and vaccines, including for chronic and rare diseases. All while having the ambition to be a sustainable partner in healthcare worldwide.

Job Description

The main function of this role is to contribute to organizational objectives by ensuring that registrations are obtained and maintained in accordance with national and European regulations, and with the most competitive labelling possible in the shortest possible time

Responsibilities

• Acquisition and maintenance of registration; responsible for optimal process direction

• Lifecycle management and registry strategy, you will contribute heavily to PPM & PI strategy

• Commercial compliance, bearing responsibility for the availability of the most up-to-date packaging and information leaflet on the market

• Planning & reporting; problem identification and priority setting, providing relevant information for headquarters and branch office

Requirements

• Fluent Dutch is non-negotiable!!

• 4-5 Years experience in Regulatory Affairs (both on a local and national level)

• Relevant university degree in medical, pharmaceuticals or biomedical sciences
 

Other Information

If you are interested in this job offer, please don’t hesitate to contact me for more information as soon as possible, or just click below to apply!