BE - R and D Analyst

The Clinical Release and Stability (CRS) group is a department of Small Molecule Pharmaceutical Development – Analytical Development (SMPD-AD).  

The lab team of CRS supports the delivery of the R&D portfolio by timely testing of:

- Screening studies

- Investigations

- CTA/IND – NDA/MAA stability studies

- Clinical batches for release purposes

- Risk based predictive modelling studies

- ...

Analyst Dissolution / Liquid chromatography

Your Function:

• Perform GMP analysis for screening, CTA/IND, MAA/NDA stability studies and release testing of clinical batches.
• Perform GMP analysis during product development and/or method investigation.
• Ensure compliance with regulatory requirements, GMP and safety.
• Scientific evaluation of generated results.

Your Profile:

• You hold a Master degree in Chemistry, or equivalent through experience.
• Good knowledge and practical experience with one of the following tests; Liquid Chromatography and Dissolution.
• Ensure high quality standards for experiments and take on responsibility for these experiments.
• Efficient, flexible and dynamic.
• Customer focused, and result performance driven.
• Sense of Urgency.
• You have a good knowledge of English and Dutch, both spoken and written.
• You are able to work independently, though you are also a team player.

This positions requires you to be on-site!