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Vind je volgende functie in Regulatory Affairs binnen Life Sciences en help conforme markttoegang en regulatoire excellentie te garanderen bij de toonaangevende bedrijven in België.
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 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 pharmaceutical organization specialized in innovative cell therapies, is seeking a CAR-T QA C&Q Engineer. This role focuses on ensuring the qualification status of critical production assets and managing compliance for facilities, utilities, and process equipment. The position involves acting as a quality process expert and supporting international regulatory inspections.
Our client, a global pharmaceutical organization, is seeking a professional to oversee the quality management of third-party computerized systems providers. The role ensures that all external partners meet rigorous regulatory standards and internal compliance requirements through assessments and continuous performance monitoring.
Our client, a leading pharmaceutical company, is seeking a Project Engineer to manage validation aspects for new product introductions. The role involves ensuring regulatory compliance and successful implementation across the product lifecycle, with a specific focus on assembly and packaging processes.
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 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 pharmaceutical organization, is seeking a professional to ensure the end-to-end validation of new products across formulation, filling, and packaging. This role focuses on supporting product launches through rigorous documentation, production follow-up, and quality investigations within a dynamic project environment.
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 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.
Of je nu gespecialiseerd bent in regulatory strategie, compliance of etikettering: bij ons vind je kansen in uiteenlopende specialisaties.
Regulatory Strategist – Bepaal en begeleid de regulatory strategie doorheen het volledige ontwikkeltraject.
Regulatory Affairs Expert – Bied ondersteuning bij de voorbereiding, indiening en opvolging van regulatoire dossiers.
Regulatory Affairs Specialist – Zorg voor naleving van de Belgische, Europese en internationale regelgeving voor geneesmiddelen.
Artwork & Labeling Consultant – Beheer het labelingproces en voer artworkcontroles uit volgens de geldende richtlijnen.
Labeling Specialist – Waak over correcte en conforme productinformatie voor verschillende markten.
CMC Regulatory Affairs Consultant – Verzorg de indiening van regulatoire CMC-dossiers (Chemistry, Manufacturing & Controls).
Regulatory Projectcoördinator – Coördineer deadlines, dossiers en communicatie met stakeholders.
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