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Walloon BrabantHybridHours negotiable<3months
You will support the activities of a major pharmaceutical production site. You will work autonomously within the Qualification & Validation team.
What you do
- Perform and finalize the periodic qualification review.
- Support qualification and validation activities for production, assembly, and packaging equipment, particularly for combined products.
- Write and execute qualification/validation protocols and reports.
- Ensure follow-up of the qualified status of equipment and participate in the management of deviations / CAPA.
- Guarantee the maintenance of GMP compliance and preparation for audits/inspections.
- Collaborate with operational, quality, and project teams teams.
What they ask
- Minimum 3 years of practical experience in Qualification & Validation in the pharmaceutical industry.
- Concrete experience with production, conditioning/packaging equipment, and combined products (profiles exclusively focused on laboratory equipment will not be considered).
- High autonomy, proactivity, and excellent problem-solving skills.
- Languages: Fluent French is essential, technical English (reading and writing).
How to apply
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