Vacatures in 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 fast-growing MedTech organization, is seeking a professional to establish their quality foundations and guide their initial regulatory submission. This role focuses on building a robust quality framework for an innovative surgical software platform.

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 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 seeking a professional to act as a quality liaison for internal and external activities. This role ensures the compliance and quality standards of products manufactured at partner facilities through rigorous oversight and systems management.

Our client, a prominent life sciences organization, is seeking an professional to manage the qualification and testing of Master Batch Records. The role focuses on the development, writing, and execution of test protocols within a manufacturing execution system to ensure compliance with industry standards.

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.

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 prominent pharmaceutical company, is looking for a specialist to facilitate material and supplier qualification for a specific project. This position focuses on coordinating with various workstreams to collect and evaluate information while ensuring adherence to quality standards and timelines.