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 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 life sciences organization, is seeking an expert to lead comprehensive regulatory dossier assessments and file gap analyses. The project focuses on identifying compliance risks and developing scientific justifications to support regulatory submissions and health authority responses.

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 life sciences organization, is seeking an expert to oversee validation activities for transport and CMO-manufactured products. This role ensures the compliance of validation lifecycles, protocols, and risk assessments while serving as a key technical point of contact for regulatory submissions and audits.

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 pharmaceutical organization, is seeking a QA Qualification Engineer to provide quality oversight for process and laboratory equipment. This role focuses on managing qualification activities throughout the system lifecycle to ensure strict compliance with international regulations and quality standards.

Our client, a leading MedTech organization, is seeking a Clinical Research Associate to manage clinical activities across various study sites. The role focuses on overseeing site performance, conducting monitoring visits, and ensuring the delivery of high-quality data for clinical projects.

Our client, a leading pharmaceutical organization, is seeking a dedicated professional to provide quality oversight for site facilities and utilities. This role focuses on ensuring compliance across the system lifecycle, from initial design through to ongoing maintenance and decommissioning.