Pauwels Consulting Logo
Rear view of a person in a server room at a desk, working on multiple monitors displaying code and system data.

Emplois en Digital & IT

Trouvez votre prochain poste en Digital & IT dans les Life Sciences et contribuez à stimuler l’innovation, la gestion des données et l’excellence des systèmes au sein des principales entreprises de Belgique.

12
postes vacants disponibles

Co-Development Technician

Life Sciences
Process and Manufacturing
Master
Junior (0+)

Our client, a leading pharmaceutical company, is looking for a Co-Development Technician to support multiple clinical projects. This role ensures that clinical batches and critical samples are supplied on time to clinical studies, packaging sites, and testing laboratories worldwide.

Puurs-Sint-Amands, Anvers
Consultancy
Fulltime, On-site
Postulez maintenant

R&D Method Development & Validation Specialist

Life Sciences
Lab
Master
Advanced (5+)

Our client, a leading pharmaceutical organization, is seeking an R&D Method Development & Validation Specialist to support their analytical operations. This role focuses on developing and validating robust analytical methods using state-of-the-art statistical approaches to ensure scientific excellence.

Braine-l'Alleud, Brabant wallon
Consultancy
Fulltime, Hybrid
Postulez maintenant

Cleaning Validation Engineer

Life Sciences
Validation and Qualification
Master
Medior (3+)

Our client, a leading pharmaceutical company, is seeking a Cleaning Validation Engineer to specialize in the development and optimization of cleaning processes for production equipment. The role combines technical expertise with operational support to ensure compliance and business continuity within a regulated manufacturing environment.

Heist-op-den-Berg, Anvers
Consultancy
Fulltime, Hybrid
Postulez maintenant

Associate Clinical Project Manager

Life Sciences
Clinical
Medior (3+)

Our client, a global pharmaceutical leader, is seeking an Associate Clinical Project Manager to provide comprehensive operational support in delivering clinical studies. This role involves managing the study lifecycle from protocol development through to archiving, ensuring all quality, timeline, and regulatory objectives are met.

Anderlecht, Bruxelles-Capitale
Consultancy
Fulltime, Hybrid
Postulez maintenant

CSV Validation Engineer

Life Sciences
Validation and Qualification
Master
Medior (3+)

Our client, a leading pharmaceutical company, is seeking a CSV Validation Engineer to join their team. This role focuses on the validation of software packages and computerized systems to ensure compliance with global regulatory standards.

Geel, Anvers
Consultancy
Fulltime, On-site
Postulez maintenant

CSV & Computer System Validation Specialist

Life Sciences
Electromechanical
Master
Advanced (5+)

Our client, a leading organization in the life sciences sector, is seeking a professional to oversee the quality and validation of computerized laboratory systems. The role focuses on system administration and validation activities to ensure compliance with international regulatory standards in a laboratory environment.

Geleen, Limbourg
Consultancy
Fulltime, Hybrid
Postulez maintenant

Microbiology Expert – Small Molecules

Life Sciences
Lab
Phd
Beerse, Anvers
Consultancy
Fulltime, Hybrid
Postulez maintenant

Sterility Assurance Manager

Life Sciences
Validation and Qualification
Senior (7+)

Our client, a leading pharmaceutical organization, is seeking a Sterility Assurance Manager. This role focuses on developing and overseeing the sterility assurance program to maintain safety and regulatory compliance in vaccine production. The position serves as a technical expert in microbiology and aseptic processes to drive continuous improvement across manufacturing units.

Wavre, Brabant wallon
Consultancy
Fulltime, Hybrid
Postulez maintenant

Senior Specialist Microbiology

Life Sciences
Lab
Master
Senior (7+)

Our client, a leading pharmaceutical company, is seeking a Senior Specialist Microbiology to serve as a project manager within their quality organization. This role involves managing complex microbiological topics and ensuring high standards of compliance and safety.

Herentals, Anvers
Consultancy
Fulltime, Hybrid
Postulez maintenant

Commissioning Lead

Life Sciences
Validation and Qualification
Bachelor, Master
Expert (10+)

Our client, a leading pharmaceutical company, is looking for a Commissioning Lead to drive the execution of an ambitious project. This role involves overseeing the entire commissioning lifecycle, bridging the gap between engineering, contractors, and quality departments to ensure successful delivery of critical installations.

Geel, Anvers
Consultancy
Fulltime, Hybrid
Postulez maintenant

Impact Quality Lead - GVP

Life Sciences
Regulatory Affairs
Bachelor, Master

Our client, a global biopharmaceutical organization, is seeking an Impact Quality Lead to implement and maintain a proactive approach to pharmacovigilance compliance. This role focuses on ensuring that all pharmacovigilance activities adhere to international regulatory requirements while providing strategic quality leadership across post-marketing programs.

Braine-l'Alleud, Brabant wallon
Consultancy
Fulltime, Hybrid
Postulez maintenant

External Research Opportunity Lead

Life Sciences
Administration

Our client, a leading pharmaceutical organization, is seeking an External Research Opportunity Lead to manage the end-to-end lifecycle of external research collaborations. This role ensures that all projects align with strategic goals and adhere to strict compliance and regulatory requirements across multiple therapeutic areas.

Anderlecht, Bruxelles-Capitale
Consultancy
Fulltime, Hybrid
Postulez maintenant

Expertises en Digital & IT

Concevez, implémentez et validez des systèmes digitaux qui supportent la production GMP, garantissent l’intégrité des données et permettent des opérations efficaces et conformes dans les environnements Life Sciences.

MES Consultant – Mettre en œuvre et optimiser les MES pour soutenir une production efficace et conforme.

CSV Consultant – Valider les systèmes GxP et garantir des solutions digitales conformes aux exigences réglementaires.

MES Specialist – Configurer et maintenir les MES pour soutenir les opérations de production.

MBR Editor – Créer et mettre à jour des dossiers de lots électroniques précis.

MBR Designer – Concevoir des workflows électroniques structurés et conformes.

MBR Reviewer – Examiner et approuver les dossiers de lots électroniques pour leur exactitude.

Master Batch Editor – Maintenir et mettre à jour la documentation Master Batch.

Master Batch Reviewer – Garantir la qualité des dossiers de lots conforme aux GMP.

A man with curly hair and glasses works on a laptop at a long table in a modern, open office space with large windows and a high ceiling.

Rencontrez Alex & trouvez les offres qui vous correspondent

Vous cherchez votre prochaine étape sans savoir par où commencer Alex vous aide à trouver des opportunités pertinentes même sans CV mis à jour.