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Find your next Qualification & Validation role in Life Sciences and help ensure compliant, reliable, and high-quality processes across Belgium’s leading companies.
Whether you're passionate about process validation, computer system validation, or equipment qualification, we have opportunities across multiple specializations:
Process Validation Specialist – Validate manufacturing processes and ensure consistent product quality.
Cleaning Validation Engineer – Develop and execute cleaning validation protocols and studies.
Commissioning Manager – Lead commissioning activities for pharmaceutical facilities and equipment.
CQV Manager – Manage commissioning, qualification, and validation projects end-to-end.
CSV Consultant – Validate computer systems and ensure data integrity compliance.
Risk Assessment Specialist – Conduct risk assessments for validation and qualification activities.
Compliance Engineer – Ensure validation activities meet GMP and regulatory requirements.
Equipment Validation Specialist – Perform IQ, OQ, and PQ for manufacturing equipment.
Cleanroom Validation Specialist – Qualify and validate cleanroom environments and HVAC systems.
Computer Validation Consultant – Validate computerized systems and software applications.
Validation Coordinator – Coordinate validation projects, documentation, and timelines.
MBR Editor – Create and edit Master Batch Records for manufacturing processes.
MBR Designer – Design comprehensive Master Batch Records and production documentation.
MBR Reviewer – Review and approve Master Batch Records for accuracy and compliance.
Master Batch Specialist – Develop master batch documentation and recipes.
Validation Project Manager – Lead validation projects from planning through execution and closure.
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