GMP Auditor 17

Profile: Experienced Pharmaceutical GMP and Quality Auditor, with a demonstrated history of working in the administration of drug factories inspection “DFI” at Egyptian Drug Authority “EDA”. Being well educated, extensively trained and highly experienced in the field of pharmaceutical quality, I can perform all shop floor quality activities, ensure cGMP compliance, lead QMS implementation, lead Quality Risk Management activities, revise and issue the SOPs for all departments, review and release batch records, prepare Annual Product Review reports, drive continuous improvement and enhancement efforts, initiate, review and approve deviation reports, investigations, CAPAs and change control reports, review and approve various validation and qualification activities (process validation, cleaning validation, equipment qualification, utilities qualification, etc.), ensure regulatory compliance, support regulatory agency inspections, conduct internal and external audit runs as lead auditor, prepare technical reports about the status of the factory, report monthly progress, train new QA officers, and much more. Can be working all over the world. Based in Egypt. Languages known: Arabic - mother tongue English - Excellent professional.