Our client is a professional organisation, based in Anvers Belgium. The company is part of a global pharmaceutical company, active in injectable pharmaceuticals.
This interim project will take up to 5 months to cover for maternity leave. You will be part of a regulatory and quality department that is responsible for all products in the Benelux.
To make sure that the department remains able to take on the daily workload, you will be required to work preferably full time and on location at the facility in the Antwerp region.
You will be responsible for the continuity of writing variations for the directions, labels and dossiers. Translations need to be taken care of as well.