As part of our growth in Belgium, we are looking for a process Validation and equipment Qualification consultant to be involved in our development in the pharmaceutical industry.
Your main tasks and responsibilities are:
- Defining the Qualification and Validation approach;
- Establishing procedures for qualification and validation in accordance with international standards (GMP, FDA);
- Writing qualification/validation documents;
- Coordinating and executing qualification and validation tests.
An Engineering degree and a first experience in the same area of expertise is required.
The successful candidate is autonomous and holds good written and oral skills in english.
Ability to work in dutch is an asset.