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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.
Our client, a leading pharmaceutical organization, is seeking a professional to provide commercial manufacturing support and process optimization. The role focuses on technology transfer activities to facilitate the introduction of new products and processes within a large-scale manufacturing environment.
Our client, a leading pharmaceutical organization, is seeking a professional to manage and execute validation activities for computerized systems. The project involves ensuring that all cGMP-critical software packages remain compliant with regulatory and user requirements.
Our client, a leading pharmaceutical company, is seeking a CSV Engineer to support the validation of cGMP-critical computerized systems. The role focuses on ensuring systems remain compliant with applicable regulatory and quality requirements through hands-on validation activities.
Onze klant is een internationale organisatie gespecialiseerd in de farmaceutische verpakkingssector. In deze rol ben je verantwoordelijk voor het op niveau brengen en houden van de validatiestatus van systemen, processen en installaties conform de geldende farmaceutische wet- en regelgeving.
Our client, a global biotechnology organization, is seeking a professional to support their digital technology compliance team with computer systems lifecycle management and IT quality processes. The role involves ensuring the integrity and compliance of computerized systems within a highly regulated environment.
Our client, a leading organization in the life sciences sector, is seeking a professional to ensure manufacturing processes are validated, documented, and maintained in compliance with global standards. This role involves collaborating across departments to validate new and existing processes, supporting product introductions, and maintaining a validated state throughout the lifecycle.
Our client, a leading pharmaceutical organization, is seeking an Equipment Validation Engineer to ensure the reliable and compliant operation of production systems. The role focuses on managing validation documentation and testing for mechanical equipment within multidisciplinary engineering and production projects.
Our client, a leading pharmaceutical organization, is looking for a Cleaning Validation Engineer to support their production site. This role focuses on ensuring that cleaning processes for equipment and systems are properly documented and validated in compliance with strict quality standards.
Our client, a leading organization in the life sciences sector, is seeking a professional to support computer system validation activities. The role focuses on ensuring that computerized and automated systems in GxP-regulated environments are fit for purpose and comply with both regulatory requirements and internal standards.
Onze klant, een vooraanstaande organisatie binnen de life sciences sector, is op zoek naar een deskundige voor de ondersteuning van diverse investerings- en verbeteringsprojecten. De focus ligt op het coördineren en opvolgen van alle validatie- en kwalificatieactiviteiten voor cleanrooms en technische installaties binnen een multidisciplinaire omgeving.
Onze klant, een toonaangevende organisatie binnen de biotechnologie, is op zoek naar een professional voor de kwalificatie van diverse procesinstallaties. In deze rol draagt men bij aan het projectvalidatieteam door systemen zoals bioreactoren, chromatografiekolommen en clean utilities tijdig te kwalificeren.
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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