Hybrid Analytical Scientist: Method Development in Pharma

UCB

Eigenbrakel

Hybride

EUR 55 000 - 85 000

Plein temps

Il y a 16 heures
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Avantages offerts par ce poste

Hybrid work model

Résumé du poste

UCB, based in Belgium, seeks 3 Analytical Scientists to join the ADS PCA team at the Braine-l’Alleud campus. You will develop and validate analytical methods supporting development programs from early clinical phases through lifecycle management, and contribute to digitalization of analytical processes.

You will collaborate with scientists, analysts, QA, and project stakeholders; you will test materials and products, support stability studies, and ensure GMP compliance.

Qualifications

  • Bachelor’s or Master’s degree in Analytical Chemistry or related scientific discipline.
  • 2–5 years of experience in the pharmaceutical industry.
  • Hands-on expertise in analytical method development for chemical and biological products.
  • Understanding of GMP, pharmacopoeias, method validation, transfer, and regulatory requirements.

Responsabilités

  • Develop and validate analytical methods for pharmaceutical products across development stages.
  • Perform analytical testing of raw materials, intermediates, and finished products.
  • Support stability studies, clinical releases, and process understanding activities.
  • Analyze data, challenge results, and generate meaningful scientific insights.
  • Manage analytical documentation, protocols, reports, and GxP-compliant records.
  • Coach colleagues, support investigations, and contribute to new technology implementation.

Connaissances

Analytical method development
GMP knowledge
Bilingual French/English
Cross-functional collaboration

Formation

Bachelor’s or Master’s degree in Analytical Chemistry

Outils

Chromatography
Electrophoresis
Spectrometry
Dissolution testing

Description du poste

UCB, based in Belgium, seeks 3 Analytical Scientists to join the ADS PCA team at the Braine-l’Alleud campus. You will develop and validate analytical methods supporting development programs from early clinical phases through lifecycle management, and contribute to digitalization of analytical processes.

You will collaborate with scientists, analysts, QA, and project stakeholders; you will test materials and products, support stability studies, and ensure GMP compliance.

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