Abbas Ibrahim

warehouse professional at sanofi

Cairo, Egypt

golden tex wool co.

Dec 2020 - Jun 2025 -4 yrs, 6 months

Job Details:Perform all qc tests in colors lab. Preparation of dyes used for dying the wool after analyzing the relevant samples. Approving prepared dyes according to its results using electronic system for color analyzing and visual inspection.

sanofi

Egypt

Job Details:Daily wh tour for any finding significant or non-significant. Daily logbooks checkup for all wh activities including wh temperature and rh monitoring. Deviations issuance for any non-compliant process or issue, capas implementation and closure using the quality electronic system (qualipso). Leading supervisors and operators for the right handling of incoming starting materials (raw & aux.), semi-finished, packaging (primary and secondary) materials and finished goods receiving from production handling and shipping to the distribution center according to the approved procedures and quality standards. Handling of different processes of materials through sap system. Participating in release and implementation of the ems system in the wh, updating the relevant sops and creating the required attachments for recording. Leading the process of annual count for all wh different materials according to the approved procedures.

al-jamjoom pharma

Egypt

Job Details:A member of qa team who started up jamjoom pharma factory (egypt site) after eda license approval. Creating and reviewing sops & batch records. Sites’ layouts reviewing against room data sheet before approving. Quality tours (gemba) at the factory (warehouse, dispensing area, sterile, solid & semi solid areas) finding any quality issues. Initiation, investigation and following up capas implementation for deviations, qrms & ccrs. Participating in internal and external audits for the factory different suppliers then following up the findings capas implementation. Performing ipc executive responsibilities starting from raw materials dispensing till finished products delivery verifications to the warehouse. Creating materials’ manufacturers and their related part numbers on sap system.

rotabiogen

Job Details:A member of qa team who started up rotabiogen factory after eda license approval. Responsible for calibration of all instruments in rotabiogen factory, creating and following up the calibration plan. Creation of sops. Sites’ layouts reviewing against room data sheet before approving. Reviewing products packaging materials before approving. IPC specialist responsible for: control the process in the sterile area starting from lines clearance, dispensing of materials, preparation until reaching the semi-finished product in the two sterile lines (ampoule and vial) according to gmp & batch manufacturing record rules/instructions. Controlling the process of packaging area starting from visual inspection until finished product delivery to the warehouse according to gmp & batch packaging record rules/instructions. Sampling in each process starting from major lines cleaning, preparation, filling until finished products. Monitoring of hvac in the production area and controlling any problem may affect the production process. Batch record reviewing.