Tarek Muhammed Salah Ayoueb

A Quality Control specialist in Blood Product Control UnitFull Time

• Job Details:Responsibilities: 1) Receiving samples for analysis from other departments, like LR "Lot Release department", MA "Marketing Authorization department" and PMS "Post Marketing Surveillance department" and recording them in logbook to do the needed tests in certain timetable. 2) Monitoring and recording Temperature and Humidity of working sections and temperature of Refrigerators. 3) Doing Viral Safety tests {HCV, HIV-1 & HIV-2 & HBsAg} by using ELISA Technique "Enzyme-Linked Immuno-Sorbent Assay". 4) Doing Purity test by using "SDS-Page electrophoresis stained by Coomassie stain" technique. 5) Doing Identity test by using "Gel Immunoelectrophoresis" technique

R & D Specialist at Stability departmentFull Time

• Job Details:Responsibilities: 1) Doing stability studies of different dosage forms like tab, cap, syrup, suspension, cream, ointment and ampoules. 2) Doing different chemical tests like assay. dissolution, and related impurities of compound 3) Doing different physical tests like disintegration, hardness, friability, PH, viscosity of creams & ointment, water content test and specific gravity. 4) Calibration of PH and balance daily. 5) Doing follow-up of Accelerated and Long term stability studies. 6) Doing Out of specification ‘OOS’ reports for any unsuccessful trials and reporting notes and suggestions if found. 7) Monitoring Temperature & Humidity of Stability Chamber ‘Long Term Room’ and Stability Cabinet ‘Accelerated Room’ daily and checking water level. 8) Monitoring data loggers of Temperature and Humidity monthly. 9) Responsible for entering and withdrawing of any sample from stability rooms for any research reason. 10) Responsible for storage Accelerated samples for 06 months and Long-Term samples for one year after end of their studies. 11) Receiving new columns of stability and doing list of needed columns or exhausted columns.

Quality Assurance In-Process Control SpecialistFull Time

• Job Details:Responsibilities: 1) Responsible for applying GMP in each step in any area. 2) Receiving, weighing, dispensing different raw materials and packaging materials in the warehouse according to batch record and condition of each material and checking dispensing cards. 3) Receiving different raw materials and packaging materials in manufacturing areas, checking their weight according to batch record and revising dispensing cards. 4) Checking Temperature and humidity of each area before working. 5) Checking calibration of balances and checking calibration due-date of each instrument 6) Monitoring each step in manufacturing area and doing specific tests for dosage forms according to batch record and SOP: a) Solid area: {Tablets: Mixing, tableting, moisture content of mixed powder and average weight, hardness, disintegration, friability of tablets and leakage test for strips} {Capsules: Mixing, filling of capsules, moisture content of mixed powder, average weight of empty capsules and filled capsules, disintegration and leakage test for strips} b) Syrup & Suspension area: {Average filling volume, PH, leakage of bottles and Torque test} c) Eye Drops: {PH & check volume} d) Packaging: {checking insert, packaging materials, batch number, price of each product, manufacturing & expiration date, number of units in one box & one carton and doing delivery form for warehouse} 7) Revising batch record before sending to IPC section head. 8) Reporting problems in a Deviation Report and solution.