Emplois en Regulatory Affairs

Our client is a specialized knowledge partner based in the province of Limburg, guiding international suppliers through the registration of biocidal products on the EU market. You'll be joining a small, ambitious team where in-house regulatory expertise is the core of what they do and where there's real room to take ownership as the organization grows into adjacent regulatory frameworks and international markets.

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 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 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.

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 organization, is seeking a Development Analyst to join their analytical development team. The role focuses on the development, validation, and transfer of robust physico-chemical methods for biological and chemical processes from clinical phases to commercialization.

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 life sciences organization, is seeking an MBR Qualification Engineer to support their manufacturing systems. This role focuses on the qualification testing, writing, and execution of test protocols for Master Batch Records within a manufacturing execution system.

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 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.

Onze klant, een toonaangevend farmaceutisch bedrijf, is op zoek naar een Quality Project Associate. In deze rol is men verantwoordelijk voor de kwaliteits- en productregistratieactiviteiten om de introductie van nieuwe producten te ondersteunen.