Abdelrahman Atef

Collect data of PQR and prepare PQR report. Batch record review. Follow up the environmental monitoring. Inspect production lines/areas for GMP compliance and other quality standards. Check machine/line for clearance as per written approved procedures before the start of batch manufacturing/packaging. Follow up & Performing IPC activities and testing for the different operations in the production areas (solid, liquid, semi solid, suppositories and packaging) in the plant. Controlling IPC tests as (weight variation, Friability, hardness, thickness, disintegration, torque test, calibration PH meter, measuring PH number and leakage test). Follow up all packaging activities in packaging area. Perform sampling process for all production stages (preparation, compression, coating, blistering & packaging) according to the sampling plan. Monitoring warehouse areas (Raw materials, Packaging materials and Finished product). Carry out the weighing process of raw materials to guarantee the conformity of specifications to the quality standards, approving the release of materials to production and ensuring raw material storage compliance as per guidelines. Inspection on the division of the warehouse releasing area, quarantine area and the rejection area with the true identification labels. Follow-up the sampling of raw materials and dispensing processes

Perform sampling (blood, urine, stools,semmen , other body fluids and diffrent cultures) Exert parasitological and bacteriological test analysis. performing medical chemistry tests & parasitology tests and urine culture. Manual Hematology TESTS “CBC COUNT , Differential count “ latex tests work on spectroscopy (colorimetric and kinetic).

Training in this lab as a medical analysis specialist