Jobs 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 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 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 prominent biotechnology organization, is looking for a specialist to lead activities within their stability and clinical release laboratory. The role focuses on performing and overseeing release and stability testing for products ranging from early clinical phases to phase III. The position involves collaborating in a cross-functional environment to ensure compliance with quality standards and regulatory requirements.

Our client, a leading organization in the pharmaceutical and biotechnology sector, is seeking a Validation Engineer to support the validation of equipment, systems, and processes. This role ensures that facilities, utilities, and computerized systems remain compliant with regulatory and quality requirements throughout their entire lifecycle.

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.

QA Engineer

Pauwels Consulting — Life Sciences & Pharma, België

Over de functie

Voor een groeiende farmaceutische/biotech-organisatie in België zijn we op zoek naar een QA Engineer. Je speelt een sleutelrol in het bewaken van productkwaliteit en regelgeving binnen productie- en labprocessen, in nauwe samenwerking met Productie, QC en Regulatory Affairs.

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 life sciences organization, is seeking a specialist to assess and enhance a quality management system in alignment with EU GMP requirements. The role supports inspection readiness and a manufacturing import authorization project to enable compliant processes for clinical product certification.

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.