Quality Assurance cGMP Compliance & In Process Control work is My Core, Team Leader of 8 QA Members.-Supervising the IPC process starting from analysis of raw materials, filling, packing materials & packaging materials to the finished product. -Having a full awareness about the most recent local & international requirements regarding the quality systems. -Having a good awareness of ISO 9001, 19011, 14001 , 45001 & 22716.- Perform Deviation Reports and CAPAs for non-conformity cases and follow up on these matters. -Studying the effect of the required technical changes to guarantee avoiding its negative reflect on product quality. -Performing visits to the work sites to review the commitment to the quality standards & GMP. -Performs preliminary studies to the customers’ complaints & prepares its records. -Prepares the reports of the products recall & shares in the dummy recall process & testing its efficacy. -Participates in preparation of the reports of quality management & management review reports. -Applying the company policies and work for achieving its goals according to the ethics, rules & regulations. -Following-up the application of the GMP, GLP, GSP, GDP & the SOPs in the company. -Conducting an Internal Audit and monitoring the effectiveness of CAPA. -Conducting an External Audit on suppliers and conducting the Supplier Qualification.-Participates in reviewing the quality records to ensure its fulfillment & validate its data. -Reviewing the Batches Record of all Products.-Releasing the Finished Products after ensuring the conformity of them.-Following-up the performance of the external vendors for the maintenance of the equipment & machines. -Making sure that the periodical maintenance program for the machines & equipment is done in the assigned dates and the calibration of machines is done in time. -Participates in studying the change control on the products quality before execution & doing potential Risk assessment

Lyophilized Sterile Hormone, Liquids & Powder Senior Specialist at Preparation, Filling and Packaging Units in the Lines of Ampoules, Vials & Eye Drops.-Follow up on Preparation, Filling and Packaging Processes. -Follow Up on Preparation in Olsa & Octo medical tanks.-Follow up on Bosch & EMA filling machines. -Follow up on Klee & Uosi-froid Lyphilization Instruments. -Follow up on EMA Packaging Compact Line. -Follow up on Origin segregation Machine. -Review & ensure the main system of sterile area governance. -Ensure that all machines are working under it's validated critical process parameter. -Review batch records , logbooks , charts , printouts prior to batch release. -Perform Deviation Reports and CAPAs and get the root causes. -Review batch related documentation for completeness , correctness and compliance to approved standards. -Prepares operational schedules and coordinates manufacturing activitiesConduct In Process Control Tests.-Follow up on troubleshooting in cooperating with the engineering sector and create Root Cause Analysis.

Mainly QA Compliance and QA IPC Work. -In Sterile Area Lines Of Vials & LVPs Sterile Liquid & Solid Human and Vet Products. -Control and Follow up the Receiving and Dispensing of Raw and Packaging Materials.-Follow up on Preparation, Filling & Packaging Processes. -In process control for filling and packaging of all products. -Sampling of semi finished and finished products. -Documentation and sops reviewing. -Conducting Internal and External Audits. -Final batch reviewer and batch release.- Annual Product Review Data Entry.

Military Service

As a Counselor for the Association

EPSF Step on the way Course Hosting Chairperson at EPSF ERU