Technicien Validation (H/F/X)
Description
Our client is an internationally recognised biotechnology company based in the Liège area and part of a major industrial group. It develops and manufactures proteins, nucleic acids, peptides, antibodies and reagents for research, diagnostics and the pharmaceutical industry. Its contract development and manufacturing (CDMO) activity produces clinical and commercial batches in a cGMP environment for customers worldwide. As part of the Validation team, you will be responsible for qualifying equipment across the production, quality control, logistics and R&D departments. You will plan your work in coordination with the relevant departments, setting up a schedule for the use of the equipment and resources required for each qualification. In the field, you will carry out qualifications in line with established procedures and agreed timelines, including temperature and pressure probe calibration, temperature mapping, air velocity measurements and other tests. You will then draft accurate, well-documented qualification reports and, when needed, qualification protocols. You will also oversee qualifications performed by subcontractors, both on site and externally. This is a varied, day-shift role within a young, dynamic and innovative environment, offering a comprehensive salary package and a healthy work-life balance.
Profile sought
- At least 2 years of proven experience in qualification and metrology (mandatory)
- Bachelor’s degree in a technical or scientific field is an asset
- Fluent French and good command of technical English
- Proficiency in MS Office
- Team player with strong oral and written communication skills
- Integrity and conscientiousness
- Well organised with strong attention to detail
- Analytical, solution-oriented mindset