Emplois en Digital & IT

Onze klant is een toonaangevend Belgische familiale onderneming met internationale activiteiten. Men heeft een mooie expertise in de ontwikkeling en productie van eigen farmaceutische producten voor zowel humaan als dierlijk gebruik. Daarnaast ontwikkelt en produceert men farmaceutische producten op vraag van externe partners. Ze zijn door hun klanten en partners gekend en geapprecieerd voor hun eigen kwalitatieve producten.

Je komt terecht in het R&D of QC labo binnen de dierlijke geneeskunde. 

Our client, a leading life sciences organization, is seeking a detail-oriented Scientist to specialize in chromatography data systems. The role focuses on the design, development, and validation of custom fields and reports to support complex analytical workflows and validation projects.

Validation Engineer 

Description

The Validation Engineer is responsible for the development, implementation and execution of validation activities for cGMP-critical process systems, ensuring compliance with regulatory, user and internal requirements.

This role involves hands-on validation work and the preparation and execution of validation documentation within a regulated pharmaceutical environment.

The Global Medical Head – Integrated Evidence Generation (IEG) is responsible for leading the development and execution of the integrated evidence generation strategy for a designated asset. The role ensures alignment between evidence generation activities and the overall asset strategy to deliver robust and impactful data supporting medical, clinical, and strategic decision-making.

Working at a global level, the position collaborates with cross-functional stakeholders to identify evidence gaps, prioritize research initiatives, and drive the execution of the Integrated Evidence Strategy and Execution Plan (ISEG).

The role goes beyond execution: it involves building, shaping, and structuring the function, including governance, processes, and ways of working.

The QA Scheduler acts as a key interface between Quality and Supply Chain, ensuring that quality-related activities do not delay product release.

Our client, a leading pharmaceutical organization, is seeking a technical expert to provide project-driven support for robust manufacturing operations. This role focuses on sustaining on-market medical devices and combination products through technical improvements, process changes, and risk management activities. The position acts as a bridge between production and R&D to facilitate product launches and ensure continuous improvement.