Job Description

Distribution of samples received from production, follow up recording them in the daily record logbook, following up their analysis according to approved specification, revision, and signature of reports. Following up commitment to GMP, GLP, EHS rules. Supervising the internal and external calibration of instruments according to calibration plan, revising their certificates of calibration, and following 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 chemicals to provide upon use. Supervising the recording in the daily records [log book] Supervising training of new analysts, completion & updating of training file. Revision and signature of analysis methods excel & oracle for internal & toll manufacturing products revision& signature of annual and monthly reports supervising preparation and factorization of volumetric solutions & reagents and recording in their logbook. Supervising the issue of all SOPs specified for all instruments used in the department. supervising the implementation of procedures specified for internal & external audits toll manufacturing – M.O.H & foreign companies. Commitment to replacement and delegation in case of Q.C. manager absence in the finished product department..

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