Travailler en Validation

Our client, a leading pharmaceutical organization, is seeking a senior expert to support their production and supply chain facility. This role focuses on providing quality oversight and acting as a subject matter expert for cleaning validation activities to ensure regulatory compliance and reliable supply.

Our client, a leading manufacturer of pharmaceutical production equipment, is seeking validation professionals to support their automated systems. The project focuses on testing complex machinery on both physical and simulated platforms within a strictly regulated environment.

Our client, a leading global healthcare organization, is seeking a specialist to manage logistics quality compliance and deviation management. The role focuses on driving the full lifecycle of non-conformances and root cause investigations to ensure operational excellence within a regulated supply chain environment.

Our client is seeking a Project Documentation & Validation Coordinator to join their engineering team. The role involves managing project documentation and executing validation activities to ensure compliance across various engineering disciplines.

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.

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 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.