Job description
As a QC Analyst, you will be part of an enthusiastic team that is responsible for performing analytical tests on finished medicines, with the aim of monitoring the quality of a medicine during its release and shelf-life under different storage conditions. You report to the Supervisor Chemical Lab.
You are responsible for:
* Quality control of raw materials and medicines (suspensions, liquids, ointments, powders, tablets) according to established specifications and analysis protocols (HPLC, UPLC, GC analyses, titrations and small testing)
* Processing and reviewing data and conducting lab research in case of deviating results in collaboration with the QC compliance officer
* General functioning of the lab and lab equipment so that it is guaranteed that all analyses can take place correctly and on time
Job requirements
Do you have these talents?
* Positive, pragmatic, accurate and flexible
* You are able to critically evaluate and report scientific data
* Your way of verbal and written communication is clear and to-the-point
* You have a sufficient command of Dutch and English
* You are not allergic to penicillins or penicillin derivatives
Do you match the required education and experience?
* You have a Bachelor's degree in Chemistry, a Bachelor's degree in Pharmaceutical and Biological Laboratory Techniques or a similar degree programme
* At least two years of work experience in a similar position in a pharmaceutical lab is desirable, experience as a data reviewer is a plus.
* Good knowledge of chromatographic techniques (HPLC, UPLC, GC)
* Knowledge of GMP regulations is a plus
* Knowledge of Empower and SAP is a plus