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Find your next Manufacturing role in Life Sciences and help deliver efficient, compliant, and high-quality production processes across Belgium’s leading companies.
Our client, a prominent pharmaceutical organization, is looking for a hands-on Production Engineer to provide first-line technical support. This role ensures the continuity of the production line by troubleshooting process issues and coordinating team activities within a regulated environment.
Our client, a leading pharmaceutical organization, is seeking a professional to focus on the development and optimization of production processes for biologic products. This role supports high-quality manufacturing operations across formulation, upstream, and downstream environments.
Our client, a leading life sciences organization, is seeking a QA Operational Readiness Officer to support the start-up of a new production facility. The role focuses on providing comprehensive quality documentation review and hands-on operational support during the facility qualification and start-up phase.
Our client, a leading organization in a regulated industry, is looking for a Data Operations & Orchestration Specialist to manage critical master data elements. This role ensures that data integrity within the project enables optimal material planning, production, and financial processes through efficient coordination and system maintenance.
Our client, a prominent pharmaceutical organization, is seeking a Quality Specialist Operations to focus on quality oversight and project support. The role involves managing operational quality tasks and ensuring compliance within a strictly regulated production environment.
Our client, a leading pharmaceutical company, is seeking a professional to oversee clean utilities projects. This role focuses on the design, implementation, and verification of critical utility systems to support pharmaceutical production while ensuring high standards of safety and quality.
Our client, a leading pharmaceutical organization, is seeking a MBR Coordinator to support the startup of a new production facility. The project focuses on ensuring quality readiness, operational excellence, and regulatory compliance during the commissioning phase. This role is essential for managing the transition to operational status through meticulous batch record oversight and GMP adherence.
Our client, a leading pharmaceutical organization, is looking for a professional to support clinical development projects. The role focuses on ensuring that clinical batches and samples are manufactured, documented, and supplied to research sites and laboratories worldwide.
Our client, a leading pharmaceutical organization, is seeking a QA Officer to provide quality documentation support and operational quality assurance. This role focuses on maintaining high standards through risk assessments and documentation review while staying connected to the shop floor.
Our client, a leading life sciences organization, is seeking a senior leader to oversee the final phase of a major manufacturing project. This role ensures a compliant transition from capital project delivery to operational readiness through structured qualification and documentation closure.
Onze klant, een vooraanstaande organisatie binnen de life sciences, is op zoek naar een QA Specialist ter ondersteuning van kwaliteitsborging tijdens productiecampagnes. De focus van de rol ligt op het waarborgen van de naleving van regelgeving door een effectieve afhandeling van deviaties en procesondersteuning.
Onze klant is een gespecialiseerd productiebedrijf binnen de voedingssector. In deze rol ben je als expert verantwoordelijk voor het optimaliseren van een semi-automatische productielijn door middel van data-analyse, procesverbetering en changemanagement.
Build, operate, and improve GMP-compliant manufacturing processes that deliver safe, high-quality life sciences products at scale.
MBR Editor – Create and update GMP-compliant Master Batch Records.
MBR Designer – Design clear, structured, and compliant Master Batch Records.
MBR Reviewer – Review and approve Master Batch Records for accuracy and compliance.
Master Batch Record Specialist – Manage and optimize Master Batch Records lifecycle.
Production Technician – Execute GMP manufacturing processes safely and consistently.
Production Specialist / Lead – Lead production teams and drive shop floor excellence.
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