1. Personal Data:
 Name : Mohamed Ahmed Mustafa Ali
 Birth date: 9 /1/1982
 Home Address : El Radwan st. – El Hanoville –Alexandria.
 Home Phone : 002/034396251
 Cell Phone : +201210823456 - +201028788200
 Military Service : Exempted
 Marital Status : Married
 E-Mail : chem.m.mostafa@gmail.com -
chem.m_mostafa@yahoo.com
Qualifications:
 Education : B.Sc. with Good degree (72%)
 Faculty of Science
 Chemistry & Microbiology Department
 Alexandria University
 Graduation Year : May 2003
Language & Computer Skills:
 Mother Tongue : Arabic
 Foreign Language : Good command of English language (Spoken & Written)
 Having Course In Windows & Office (Word – Excel – Power Point – Access)
 Good Dealing with Internet
Courses
 Training in Water Treatment Station (Bab Sharki)
 Training in El Zahraa Medical Lab.
 Attended course in " Laboratory and scientific applications in medical tests field"
 Attended course in " Public health and first aid " from 12/12/2003 to 15/12/2003
 Attended course in cGMP
 Attending course in " Six Sigma – Green Belt "
 Attending online courses in " An Introduction To Operation Management "
 Attended course in Training of the trainers ( TOT)
 Lecturing Courses in :
1- Time Management
2- Strategical Planning
3- Team Work management
4- Communication Skills
5- Stress Management Skills
6- Presentation Skills
Curriculum Vitae

2. Past Experiences:
 Working as Chemist in Paints Company (El Khalil company) (2003-2004)
 Working as Chemist In Borg Pharmaceutical Company in In-process control department
from 2004 up to 2007
 In Solid dosage forms – Semi solid dosage forms – Liquid dosage forms
 Carrying out the examinations during the manufacturing steps and finish product
 Carrying out the calibration of the QC equipments
 Follow up the packaging of the finish product
 From 2007 up to 2013:
The Head Unit Of In-process control of liquid dosage form in ( Borg
Pharmaceutical company) – Quality Control Directorate
 From 2013 up to present :
The Head of In-process control department - Quality Control Directorate
 Preparing the standard operating procedures SOP and follow up its
implementations
 Supervise the implementation of cGMP during manufacturing steps
 Revise and approve the calibration sheets of all equipments in the dept.
 Revise and approve the follow up sheets of the physical examinations
during manufacturing steps
 Revise and approve the follow up sheets of examination of washing of
production equipments
 Provide the needs of the department :New equipments , Spare parts ….etc
 Overseeing the administrative affaires of the department