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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.
Onze klant, een innovatieve organisatie binnen de life sciences, focust op de digitale transformatie van hun papieren processen. In deze rol ondersteun je de uitrol van een softwarepakket voor digitale formulieren en draag je bij aan de toekomstbestendigheid van de site.
Our client, a leading pharmaceutical manufacturing organization, is seeking a process owner for their site-wide quality systems. This role focuses on driving compliance and continuous improvement for validation processes while serving as a subject matter expert during regulatory inspections.
Our client, a leading pharmaceutical company, is seeking a professional to reinforce their biologics production department. This role focuses on the end-to-end management of production deviations, requiring a strong presence in the field to investigate and resolve technical issues.
Onze klant, een toonaangevende organisatie in de farmaceutische sector, is op zoek naar een analytische professional voor een rol gericht op cleaning validatie. De focus van deze functie ligt op het uitvoeren van chromatografische analyses en het waarborgen van kwaliteitsstandaarden binnen een gereguleerde omgeving.
Onze klant, een toonaangevende speler in de biofarmaceutische sector, is op zoek naar een CQV Engineer voor de kwalificatie van kritische systemen op een nieuwe productiesite. De rol richt zich op het waarborgen van de kwaliteit en conformiteit van diverse procesapparatuur en faciliteiten gedurende de opstartfase.
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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