Job Description

Distribution of samples received from production, follow up recording them in the daily record log book, follow of their analysis according to approved specification, revision, and signature of reports. Follow up commitment to GMP, GLP, EHS rules. Supervising the internal and external calibration of instruments according to calibration plan, Follow up their certificates of calibration, and follow up their maintenance. Supervising standards used for analysis, their validity period, and their certificates to provide upon use. Follow up on all the department requirements as lab supplies, instruments, glassware, and chemical to provide upon use. Supervising the recording in the daily records logbook. Supervising training of new analysts, follow up oracle application, and complete file of training. Revision and signature of analysis method excel & oracle. Follow up the preparation of volumetric and reagent solution and factorization of them and recording in their logbook. Supervising the issue of all sops specified for all instruments used in the department. Follow up the implementation of procedures specified for external audits toll manufacture – M.O.H & foreign companies. Commitment to replacement and delegation in the case of Q.C. manager..

Requirements:

Bachelor degree in pharmacy or science Strong attention to detail. Good mathematical skills. TeamWork Problem Solving. Good Communicator. Commitment to Safety V. Good English. Good Computer / other software sills