Description
The Quality Control Analyst (Laboratory) will independently perform non-chromatographic and chromatographic chemical tests on raw materials and finished pharmaceutical products, document results in accordance with cGMP and GLP guidelines, and support product release. The role requires a professional bachelor's degree in a relevant pharmaceutical or laboratory science field, at least one year of GMP laboratory experience, strong accuracy and problem-solving skills, and proficiency in Dutch, English, MS Office, and LIMS. The position is based in Puurs-Sint-Amands and offers benefits including hospitalization insurance, vacation, training, and the possibility of working from home depending on the project.
