Eurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA.
Group's key figures are approx. 3.8 billion Euros turnover, over 800 laboratories across 47 countries and about 45,000 staff.

Eurofins Amatsigroup is one of the leading CDMOs in Europe providing high-quality, customized drug development solutions for specialty and biopharma clients. Our focus is to support clients on the earliest phases of their development pathway (from API to the clinical packaging).
Its Belgian subsidiary, Eurofins Amatsigroup NV, is based in Ghent, offering a complete drug development package for new drug entities (biological and chemical) up to early clinical phases to third parties to help them in speeding up the development and manufacturing of their drugs.

Eurofins Amatsigroup wishes to enforce its team with a QC Analyst. We are looking for a person that reports to the QC Manager of Eurofins Amatsigroup NV.

His/her main responsibilities are:

• You perform Quality Control activities according to instructions, procedures and protocols in compliance with the GMP principles and the Quality Management System.
• You perform Quality Control analyses.
• You perform ICH compliant stability studies.
• You validate analytical methods to support the quality control and release of drug products for use in clinical trials.
• You support preparation of the applicable protocols and reports.
• You accurately report, document and review the analytical test results.
• You support the maintenance, calibration and qualification of the analytical equipment.

• Professional Bachelor degree in biomedical laboratory technology, chemistry or pharmaceutical sciences with a minimum of 5 years relevant professional experience.
• Experience in a regulated Quality Control laboratory and experience with core pharmaceutical analytical techniques (HPLC/UPLC, Dissolution) is a must.
• Experience with Empower processing software is a must.
• Experience with KF, Particle sizing, UV spectroscopy, etc. are real assets.
• You are punctual and are able to work independently after a training in matters entrusted to you.
• You are flexible, problem solving and quality minded.
• You are fluent in Dutch and English (written and spoken).

• Work in a fast growing organization
• A position with responsibility within a dynamic company
• Personal development through learning on the job and additional external trainings
• A market oriented compensation