Consultant
IT fusion
Total years of experience :10 years, 9 Months
Working in compression unit.
Evaluation of compressed tablets by measure weight, hardness, disintegration and friability in inter process lab(I.P.C.).
Working at coating unit.
Preparing coating solutions.
Evaluation of coating tablets by measure weight, hardness, disintegration,
friability in inter process lab (I.P.C.).
Working with research and development department to update formula and evaluated new formula.
Writing Knowhow of each product, and writing batch record for each batch.
Planning of short term stability study (accelerated stability study) by using incubator chambers.
Preparing analysis methods for stability study using reference book (H.P.L.C indicating assay and British pharmacopoeia, U.S.P.).
Evaluation of dissolution, disintegration, moisture content, friability and content of active ingredients.
Writing standard operation procedure (S.O.Ps) for stability analysis.
Working with process validation team.
Planning process validation by writing plan master validation and
Validation protocol.
Organize sampling method and analysis.
Evaluation bulk of product by measure content of active ingredient.
Evaluation moisture of product in dry oven chamber.
Evaluation compressed tablets by measure hardness, disintegration,
friability, dissolution, moisture and content of active ingredient.
Writing validation reports.
C.I.D pharmaceutical company, Asyut
Researches and quality control sector, pharmaceutical quality control department
•Responsible for preparing of chemical reagents and theirs calibration.
•Responsible for writing S.O.Ps for each reagent preparing.
•Responsible for analysis raw materials in ware house and releasing analysis certification.
•Responsible for analysis finished products from production sector using spectrophotometer and H.P.L.C., hardness tester, moisture analyser, P.H. meter, polarimeter, disintegration tester, dissolution tester, and friability tester.
•Responsible for release analysis certificate for each batch.
•Responsible for doing periodical calibration for weighing balances, P.H. meter, spectrophotometer, polarimeter, Karl fisher and H.P.L.C.
•Responsible for daily evaluation of lab. temperature and humidity.
•Responsible for analysis water from water station in the factory.
February 2014_December 2014
C.I.D pharmaceutical company, Cairo
researches and quality control sector, methodology department
•Responsible for applying new methods for analysis finished products.
•Responsible for updating methods of analysis.
•Using reference books(U.S.P,
Responsible for applying new methods for analysis finished products.
Responsible for updating methods of analysis.
Using reference books(U.S.P, B.P, European pharmacopoeia and Chinese pharmacopoeia).
Planning method validation by running linearity, precision, accuracy, limit of detection (L.O.D), limit of quantification(L.O.Q), by using H.P.L.C.
Preparing standard operation procedure(S.O.P) for product.
in pharmacy