ELN Developer – Laboratory Digitalization & Integration
Walloon Brabant
Life Sciences - Analysis
Bachelor
Work experience: 7-10
Reference number: 93575

Our client, a major player in the pharmaceutical sector, is looking for an expert to drive the digital transformation of their laboratory environments. The role focuses on developing and integrating electronic laboratory notebooks to automate data flows between bioreactors, chromatography systems, and central databases.

Your responsibilities:

  • Develop and maintain templates, workflows, and technical components for Electronic Laboratory Notebook systems.
  • Support the implementation and configuration of laboratory digitalization tools across various scientific departments.
  • Execute the migration roadmap from desktop clients to cloud-based web interfaces.
  • Integrate laboratory equipment and devices with central data platforms using APIs and system connectors.
  • Collaborate with scientists and laboratory technicians to translate complex workflows into digital solutions.
  • Track project progress and development tasks using Azure DevOps in alignment with digital leadership.

What are we looking for?

  • 8+ years of hands-on development experience with ELN systems, with a strong focus on IDBS.
  • Proven track record in laboratory digitalization projects and system integrations within a scientific environment.
  • Technical proficiency in connecting laboratory hardware with digital ecosystems and data platforms.
  • Experience working in CMC Development environments including cell culture, purification, or formulation labs.
  • Ability to bridge the gap between technical IT requirements and scientific end-user needs.
  • You are proactive, autonomous, and possess a solution-oriented mindset.
  • You are fluent in French and English.

Nice to Haves

  • Experience with Biovia or other ELN platforms.
  • Knowledge of Sample Management or MES systems.
  • Hands-on experience with Azure DevOps.
  • Understanding of on-premise to cloud infrastructure transitions.
  • Willingness to obtain deeper knowledge of pharmaceutical manufacturing regulations.

What do we offer?

  • Start date: ASAP (February-March)
  • Duration: Until December 2026 (extensions possible)
  • Work regime: Full-time
  • Location: Braine-l'Alleud
  • Working model: Hybrid (Mandatory 2 days per week on-site)
  • Contract: open to both permanent employees and freelancers

Célia Struelens
HR & Talent Consultant
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