After being awarded the title of Qualified Person by the Cypriot Ministry of Health I have been applying my overall experience and qualifications in providing my clients with expert opinion and services to support their operational needs and help them meet EU regulation and Good Manufacturing Practice (GMP) demands by implementing solutions in a timely and professional manner.

Main Duties:• Ensure that the Quality Control Department operates according to GMP.• Approve Quality Control procedures and other documents including amendments, Deviations and Out Of Specification investigations.• Supervision of analysis of raw materials and approval of corresponding documents.• Supervision of analysis and EU release of finished products as well as approval of corresponding documents.• Supervision of on-going and ICH stability studies and approval of corresponding documents.• Approve protocols, reports and other documents corresponding to the performance of process validations, cleaning validation, analytical method validations and analytical method transfers.• To ensure proper qualification of Vendors and monitoring of their qualification status.• Ensure that all the activities of the Quality Control Department are performed in an efficient and timely manner.• Liaise with customers or suppliers in case of any issues where the Quality Control Department is involved.• Prepare the yearly budget of the Quality Control Department based on the available information and monitor its implementation.The Quality Control Department has been successfully audited by the Cypriot authorities, as well as the authorities of other countries and Delorbis’ customers.