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Emplois en Regulatory Affairs

Trouvez votre prochain poste en Regulatory Affairs dans les Life Sciences et contribuez à garantir un accès au marché conforme et une excellence réglementaire au sein des principales entreprises de Belgique.

27
postes vacants disponibles

Regulatory Affairs Specialist – Biocides & Expansion Markets

Life Sciences
Regulatory Affairs
Bachelor, Master
Advanced (5+)

Onze klant is een gespecialiseerde kennispartner die fungeert als de toegangspoort tot Europa voor internationale producenten van biociden en gewasbeschermingsmiddelen. In deze groeiende organisatie met een vlakke structuur krijg je de kans om een cruciale rol te spelen in de registratiestrategie en de uitbreiding naar nieuwe markten zoals veterinaire toepassingen. Je komt terecht in een team van experts waar inhoudelijke diepgang en een ondernemende aanpak de standaard zijn.

Limbourg
Permanent
Fulltime, On-site
Postulez maintenant

Quality Operational Readiness Engineer

Life Sciences
QA
Bachelor, Master
Medior (3+)

Our client, a pharmaceutical organization, is seeking an experienced professional to ensure quality readiness and compliance for the startup of a new production facility. The role coordinates quality-related activities during the facility qualification phase to ensure a seamless transition from construction to operational status. This position maintains full regulatory compliance and GMP standards throughout the commissioning process.

Geel, Anvers
Consultancy
Fulltime, On-site
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Senior Program Manager Sustainability

Life Sciences
(Project) Management
Bachelor, Master
Senior (7+)

Our client, a leading pharmaceutical organization, is seeking a Senior Program Manager to support a global sustainability program for packaging and devices. The role involves translating complex environmental regulatory requirements into actionable strategic roadmaps, resource plans, and implementation timelines. The project focuses on ensuring long-term compliance and operational readiness across a matrixed global supply chain.

Beerse, Anvers
Consultancy
Fulltime, Hybrid
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Launch Excellence Project Engineer - Validation

Life Sciences
Validation and Qualification
Master
Medior (3+)

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.

Puurs-Sint-Amands, Anvers
Consultancy
Fulltime, On-site
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Validation Engineer

Life Sciences
Validation and Qualification

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.

Anvers, Anvers
Consultancy
Fulltime, Hybrid
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Computer System Validation (CSV) Engineer

Life Sciences
Validation and Qualification

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.

Anvers, Anvers
Consultancy
Fulltime
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QA Engineer

Life Sciences
QA

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.

Anvers, Anvers
Consultancy
Fulltime
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QA / Qualification & Validation Specialist

Life Sciences
QA
Bachelor, Master
Medior (3+)

Our client, a prominent player in the healthcare industry, is seeking a professional to join their quality team. The role focuses on overseeing compliance throughout the system lifecycle and managing qualification activities within a regulated environment.

Beerse, Anvers
Consultancy
Fulltime, Hybrid
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QA Qualification Engineer

Life Sciences
QA
Bachelor, Master
Medior (3+)

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.

Beerse, Anvers
Consultancy
Fulltime, Hybrid
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Launch Excellence Technician I

Life Sciences
Validation and Qualification
Bachelor
Junior (0+)

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.

Puurs-Sint-Amands, Anvers
Consultancy
Fulltime, On-site
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Process Engineer

Life Sciences
Process and Manufacturing

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.

Anvers, Anvers
Consultancy
Fulltime
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QA Officer – Quality Systems & Operations

Life Sciences
QA

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.

Geel, Anvers
Consultancy
Fulltime
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Expertises en Regulatory Affairs

Que vous soyez spécialisé en stratégie réglementaire, conformité ou étiquetage : nous proposons des postes variés dans le secteur Life Sciences.

Regulatory Strategist – Définissez et pilotez la stratégie réglementaire tout au long du cycle de développement.

Expert en affaires réglementaires – Assurez le suivi complet des dossiers réglementaires, de la soumission à l’après-approbation.

Spécialiste Regulatory Affairs – Veillez à la conformité des produits pharmaceutiques avec les réglementations belges et européennes.

Consultant Artwork & Labeling – Gérez les processus d’étiquetage et contrôlez les éléments visuels selon les exigences réglementaires.

Spécialiste en étiquetage – Garantissez l’exactitude et la conformité des informations produits sur tous les marchés.

Consultant CMC Regulatory Affairs – Préparez les dossiers réglementaires liés à la qualité, fabrication et contrôle (CMC).

Coordinateur de projets réglementaires – Coordonnez les projets, échéances et communications avec les parties prenantes.

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