1. Mostafa Omar Mohammad
14A Buildings of the Arab organization for industrialization, Makram
Ebeid, Nasr City, Cairo, Egypt.
Tel: +202-22704847 Mobile phone: +20162475675
Email: dr_mostafa_omar@hotmail.com
Education
May 2001 Bachelor degree of Pharmacy
Ain Shams University, Cairo, Egypt
Overall Grade: Very Good with the degree of
honor.
May 1996 General Certificate of Secondary Education,
St. Fatima Language School, Nasr City,
Cairo, Egypt.
Working Experience
January 2008- up to date Quality Control Supervisor, EIMC United
Pharmaceuticals.
May 2005- June 2007 Stability Analyst, Quality Control
Department, Bristol Myers Squibb Egypt
(BMSE)
September 2001- May 2005 Raw Materials Analyst, Quality Control
Department, Egyptian International
Pharmaceutical Industries Co. (EIPICO)
Summer 2000 Trainee, QA Department, AVENTIS
PHARMA, Cairo, Egypt.
Courses Studied
July 2008 Achieved Six Sigma Green Belt from Quality
America online training course with an
overall grade of 89.3%
September 2005 Acheived diploma of Total Quality
Management (TQM) from the American
University in Cairo (AUC).
April 2003 Achievement certificate of Management from
the AUC with an overall grade of (A)
Special Skills
Personal skills
I believe I am a person who:
- Has good communication and leadership
skills.
- Seeks and welcomes feedback
- Responds to coaching.

2. - Takes action to enhance performance based
on experience and feedback.
Working skills
- Strong background information on current
Good Manufacturing Practice (cGMP) and
Good Laboratory Practice (GLP).
- Excellent experience in dealing with HPLC
(Agilent & Waters), GC, UV
spectrophotometer, IR spectrophotometer,
Dissolution and Disintegration testers,
refractometer, densitometer & other lab
instruments.
Computer Skills
- Excellent knowledge of Microsoft Windows,
Word, Excel, and PowerPoint.
Language Skills
- Arabic: Mother tongue.
- English: Fluent in spoken and written.
- French: Basic knowledge of spoken and written.
Job Description in EIMC United Pharmaceuticals (current job)
- Preparation of documents for the Quality Control Department including SOPs
and testing standards.
- Preparation of a Microsoft Excel based quality management system for the
Quality Control department which performs many tasks including control on
received samples, data entry and calculation of the results of various tests
performed on raw materials, packaging materials, finished products and
stability samples.
- Participated in preparation of the laboratory for three quality audits from the
Egyptian Ministry OF Health for obtaining licenses to analyze solid dosage
forms, sterile oncology products and sterile non-oncology products and all
three audits were passed successfully with very satisfactory results.
- Team member of the company’s audit team responsible for performing
internal quality audits on the company’s different departments and performing
external audits on suppliers of raw materials and packaging materials.
- Responsible for receiving QC plan from QC manager to put an action plan for
QC lab.
- Plan for sampling and testing of newly received Raw Materials, retest Raw
Materials, Packaging Materials, intermediates, and bulk products.
- Review certificates of analysis written by analysts.
- Review new methods received for raw materials and finished products.

3. - Issue and update Quality Control Standard Operating Procedures (SOPs) and
ensure their implementation.
- Coordinate with QC Manager for the availability of all QC supplies and
needed standards.
- Orient newly hired analysts and set the plan for their qualification and training
while ensuring that training records are adequately filed and maintained.
- Perform calibration of all laboratory instruments including HPLC, UV
spectrophotometers, IR spectrophotometers and other instruments.
- Prepare stability protocols for all products.
- Perform investigation of out of specification and out of trend results and
report deviations.
Job Description in Bristol Myers Squibb
- Responsible for the full analysis of all stability lots in both routine testing
(ambient and at 30C-65%RH) and premarket studies (Ambient, at
30C-65%RH and at 40C-75%RH) and data entry on BPCS (Business
Planning and Control System).
- Responsible for the monitoring of temperature and humidity data of stability
chambers and QC refrigerators.
- Responsible for the calibration of Stability section's HPLC and dissolution
testers.
- Responsible for periodical updating of Stability section's Standard Operating
Procedures (SOPs).
Job Description in EIPICO
- Responsible for the analysis of incoming raw materials to the company's
warehouse according to the defined pharmacopeias and the preparation of
secondary standards.
- Team member in the company's bioequivalence team responsible for protocol
preparation and writing, participated in the data analysis of the results and
acted as a coordinator between team members collecting data and responsible
for the final presentation of the bioequivalence study.
Personal Data
Date of birth: 18th February 1979
Place of birth: Cairo, Egypt.
Nationality: Egyptian.
Marital status: Married.
Military Service: Exempted.
References Furnished upon request.