Quality Control Analyst

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