1-The performed of Method & validation of analytical test methods for new products.2-The performed general analysis all raw materials and all dosage forms of finish products.3-Prepared all standard solution and standardization them for working. 4-Follow up the water station and analysis the water station to ensure its specifications is according to USP and British pharmacopoeia.Estabishment the file of Registration of drug included i) Composition of drug.ii) Chemical , physical and microbiological specifications of finish productiii) Specifications and method of all analysis of product.iv) Certificates of analysis of product. v) Packaging Specificationsvi) Method of analysis of productvii) Validation of methods of analysis of product.viii) Stability study ( accelerated stability study ).5 ) Follow up the stability study of products ( accelerated stability , intermediate stability and long-term stability studies). 6 ) Performed internal calibration of lab. devices ( H.P.Lc , UV Spectrophotometer ,pH meter ,electronic Balance , conductivity meter .optical rotation , Karl Fischer and other apparatus. 7 ) Training the new analyst8 ) Writing the SOPs of q.c lab. devices 9 ) A member of the internal audit for ( iso- 9001) Technical consultancy in the Chemistry.

1 ) Performed of Method & validation of analytical test methods which used in analysis of finish products2 ) Follow up the all products ( Drugs ) during the shelf life . 3 ) Follow up the all new products ( new formula of Drugs ) and study stability of them by accelerated stability . 4 ) Training the new analyst

1 ) Follow up the all raw materials 2 ) Analysis all raw materials according to USP and British pharmacopoeia. 3 ) Report the finish analysis for accept or refuse the raw materials before introduce the production department. 4 ) Follow up the all packaging materials according the internal specification and writ the report for accept or refuse

1 ) working as analyst in ( anti-biotic department ) in The national organization for drug control & research ( NODCAR) 2 ) where follow up and analysis all anti- biotic drugs from all pharmaceuticals in Egypt and write the repot of accept to allowed supermarket

1 ) Work as chemist in Quality control lab. in the company . 2 )Preparation the standard solution and analysis the bulk products ( drugs ) before filling the products.