Overview

Responsible for the following Territories: Licences established in the Netherlands with supply and distribution into the EMEA region as well as import and export activities.

Youparticipate in the compliance with GDP/GDP-API & GMP requirements for the distribution of Medicinal Product (e.g., Drug Substance/Drug Product/Finished Product/QP Certified Finished Product) into the EMEA region as well as import and export activities.

Responsibilities