We are currently looking to recruit QC Analysts to join established pharmaceutical companies. The duties will include;
To analyse raw materials, intermediate products, in-process products, finished products, and stability samples using all necessary test instruments available in the laboratory, according to the methods indicated in internal procedures and according to EU GMP principles and guidelines
To verify the calibration status of the test instruments and the validity status of the analytic standards
To carry out the routine maintenance and calibration of the laboratory’s test instruments within the boundaries of ones’ competence
To keep updated all documentation in relation to analyses made, with their respective raw data attached thereto
To keep the laboratory documentation in good and accurate condition
To collaborate in the introduction of new analytic methodologies, optimizing the existing ones, and in analytic validations if necessary
To report to superior any abnormalities found during routine activities
