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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.

13
postes vacants disponibles

Regulatory Affairs Specialist – Biocides & Expansion Markets

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

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.

Limbourg
Permanent
Fulltime, On-site
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QA Specialist

Life Sciences
QA
Master
Medior (3+)

Our client, a fast-growing MedTech start-up specializing in surgical software, is seeking a professional to lead their quality initiatives. This role focuses on building a robust quality management system from the ground up and preparing for upcoming regulatory submissions.

Anvers, Anvers
Consultancy
Fulltime, Hybrid
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QA Operational Readiness Officer

Life Sciences
QA
Bachelor, Master
Medior (3+)

Our client, a leading pharmaceutical organization, is seeking a QA Operational Readiness Officer 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.

Geel, Anvers
Consultancy
Fulltime, Hybrid
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Project Engineer Validation (Data integrity)

Life Sciences
Validation and Qualification
Master
Medior (3+)

Our client, a leading pharmaceutical organization, is seeking a Data Integrity Project Engineer to support specialized compliance projects. This role focuses on upgrading production equipment to meet GMP standards and conducting Alcoa Assessments on various systems. The position requires a hands-on approach to validation and cross-departmental coordination within a production environment.

Puurs-Sint-Amands, Anvers
Consultancy
Fulltime, On-site
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Quality Project Associate

Life Sciences
QA

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.

Puurs-Sint-Amands, Anvers
Consultancy
Fulltime
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QA Operational Readiness Officer

Life Sciences
QA
Bachelor, Master
Junior (0+)

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.

Geel, Anvers
Consultancy
Fulltime, Hybrid
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Cleanroom Construction Specialist

Life Sciences
Civil and Construction
Master
Senior (7+)

Our client, a leading pharmaceutical company, is seeking an expert to support the construction and revamping of classified manufacturing environments. The role focuses on overseeing the technical fit-out and internal finishes of facility upgrades to ensure operational excellence.

Geel, Anvers
Consultancy
Fulltime, Hybrid
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Internal Operations Quality Partner

Life Sciences
QA
Braine-l'Alleud, Brabant wallon
Consultancy
Fulltime, Hybrid
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Microbiology Expert – Small Molecule

Life Sciences
QA
Master
Junior (0+)
Beerse, Anvers
Consultancy
Fulltime, Hybrid
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Senior Expert – GMP Certification & Pilot Plant Qualification

Life Sciences
QA
Braine-l'Alleud, Brabant wallon
Consultancy
Fulltime, Hybrid
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Supplier Quality Specialist

Life Sciences
QA

Onze klant, een toonaangevende organisatie in de farmaceutische sector, is op zoek naar een Supplier Quality Specialist om de kwaliteit van aangekochte materialen te waarborgen. De focus ligt op het uitvoeren van onderzoeken en het bewaken van de naleving van kwaliteits- en regulatoire standaarden binnen een gereguleerde productieomgeving.

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

Life Sciences
Validation and Qualification

Our client, a prominent pharmaceutical organization, is looking for a hands-on Production Engineer to provide first-line technical support. This role ensures the continuity of the production line by troubleshooting process issues and coordinating team activities within a regulated environment.

Puurs-Sint-Amands, 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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