registered as a pharmacist in Egyptdispense prescription medicines to the publicensure that different treatments are compatiblecheck dosage and ensure that medicines are correctly and safely supplied and labelled (pharmacistsare legally responsible for any dispensing errors)supervise the preparation of any medicines (not all are supplied ready made-up by the manufacturer)keep a register of controlled drugs for legal and stock control purposessell over-the-counter medicinesadvise the public on the treatment of minor ailmentsadvise patients of any adverse side-effects of medicines or potential interactions with othermedicines/treatmentsoffer specialist health checks, such as blood pressure and cholesterol monitoring and diabetesscreeningarrange the delivery of prescription medicines to patientsmanage, supervise and train pharmacy support staffmanage finance and budgetskeep up to date with current pharmacy practice, new drugs and their uses.

Inspection on the dispensing process.▪ Inspection on the division of the ware house the release area, guarantee area and the reject areawith the true identification labels.▪ Follow up the check list of the RH, Temp. at the different places at the ware house.▪ Inspection on the destruction process for the rejected finished products, raw materials andpackaging materials.▪ Inspection on the raw and packaging materials and ensure its comply with the acceptance criteria.▪ Inspection on the gowning according to the SOP.▪ Inspection on the preparation process and check the weight of the raw materials,▪ Inspection on the autoclave activities with different sterilization programs.▪ Inspection on the filling process at the filling room and ensure that the area is clean from anyprevious product and that the machine is cleaned and sterilized for the new product.▪ Check the environmental monitoring for the sterile area.Check the RH, the temp. And the Δp of all the sterile area according to its classification.▪ Check the weight, the shape and the sealing of the filled bottles.▪ Inspection on every process according to the batch record and ensure that the line clearanceprocess are completed between every product.▪ Taking the samples to the Q.C department as the bulk sample: for ph. and assay, bio burden formicrobiology.▪ Taking the samples to the Q.C department as S.F.P. sample: for finished analysis and sterilityanalysis.▪ Review the recording of all the production steps at the batch process and the batch packaging.▪ Release the batch to the guarantee area after the final reconciliation by the yellow label, then by thegreen label after the certificate of the chemical and microbiological analysis.▪ Include recording all the deviation which occurs at all the production process and writing thecorrective and preventive action.▪ Recording any complain from any customer from any product and investigate about the reason ofthe problem and solving it.

check prescriptions to make sure there are no errors and that they're appropriate and safe for theindividual patient;provide advice on the dosage of medicines and the most appropriate form of medicationparticipate in ward rounds to take patient drug histories;make sure medicines are stored appropriately and securely;supervise the work of less experienced and less qualified staff;answer questions about medicines from within the hospitaland the general public;keep up to date with, and contribute to, research and development;write guidelines for drug use within the hospital and implement hospital regulations;provide information on expenditure on drugs.