Quality Control Analyst (Chromatography)

About Xedev

Xedev is a dynamic Contract Development & Manufacturing Organization (CDMO), specialized in pharmaceutical formulation and process development. We support pharmaceutical companies worldwide in developing solid dosage forms, with strong expertise in drying, agglomeration, and coating processes, including our core technology spray drying.

As an independent development partner, we act as the bridge between customer ideas and robust pharmaceutical products. Our combination of scientific know-how, process expertise, and hands-on experience makes Xedev an attractive partner for companies looking to accelerate their development.

From our modern facility in Zele (Belgium), we continue to grow and innovate – and we are looking for talented QC analyst to strengthen our team.

We are currently installing our brand new QC lab as part of our GMP facility.

Your role as QC analyst

As a QC analyst, you play a central role within our scientific pharmaceutical product development teams. Together with the QC Manager, you are developing and validating analytical methods together with performing routine analyses. You act as the scientific reference point within the team, combining hands-on expertise with the ability to guide and inspire colleagues.

Your responsibilities include :

• Perform routine and non-routine QC analyses using liquid chromatography techniques (HPLC / UPLC), including assay, impurity, and dissolution testing.
• Conduct analytical method development and optimization for LC-based methods to support

product development and QC needs.

Profile

Why join us?

At Xedev, you will :

Ready to make an impact?

Send your CV and motivation letter to elien@xedev.com.