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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 life sciences organization, is seeking a Project Validation Coordinator for an intensive graduate program. This role focuses on coordinating validation deliverables and project scheduling to ensure the successful execution of high-quality technical projects.
Onze klant, een toonaangevende farmaceutische organisatie, is op zoek naar een gemotiveerde medewerker ter ondersteuning van diverse inspectieprocessen. De focus van deze rol ligt op de coördinatie van gevoeligheidsstudies en het bieden van administratieve en technische ondersteuning bij visuele inspectieprojecten.
Our client, a leading pharmaceutical company, is seeking an Equipment Deployment Associate to oversee the implementation of analytical equipment projects. This role ensures that equipment is selected, deployed, and released in compliance with safety, regulatory standards, and internal priorities.
Onze klant, een toonaangevende organisatie binnen de farmaceutische industrie, is op zoek naar een Validation Coördinator BES om het engineeringteam te versterken. In deze rol fungeer je als het centrale aanspreekpunt voor validatie binnen projecten gericht op gebouwinfrastructuur, elektriciteit en beveiliging.
Our client, a pharmaceutical organization, is establishing a new production facility and is seeking a specialist to provide technical quality oversight. This role ensures a seamless transition from construction phases to operational status while maintaining full compliance during the transformation process.
Our client, a leading pharmaceutical company, is seeking a Cleaning Validation Engineer to specialize in the development and optimization of cleaning processes for production equipment. The role combines technical expertise with operational support to ensure compliance and business continuity within a regulated manufacturing environment.
Our client, a leading pharmaceutical company, is looking for a Commissioning Lead to drive the execution of an ambitious project. This role involves overseeing the entire commissioning lifecycle, bridging the gap between engineering, contractors, and quality departments to ensure successful delivery of critical installations.
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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