Ahmed Adel CV

1. Phone: +2 01028092888 , +2 01003964729
+2(03)5248697
Address :-
18-Syria street – Roushdy , Alexandria – Egypt E-mail:
alo_hamada82@hotmail.com
Ahmed Adel Abd El Latif Ragab
Education
Work experiences
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 Bachelor / Pharmaceutical sciences ,
June 2004 , Alexandria University- Egypt , Major grade: Very Good.
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 Master degree : Analytical Chemistry / Pharmaceutical sciences
In Alexandria University- Egypt (In progress).
 Master in Business administration (MBA):In Brooklyn Academy (In progress).
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 October 2014 - Present:
Assistant Quality Control manager .
( European Egyptian Pharmaceutical Industry (Pharco Corporation ))
Responsible for :
 Application of International standards in Sampling & analysis procedures.
 Supervising Sampling & Analysis affairs .
 Approval of raw materials for Production use .
 Issuing & application of Standards Operating Procedures
(analysis & sampling affairs )
 Ensure that sampling & testing processes and Raw materials specifications
are met & taking corrective & preventive actions whenever needed
& managing positive release of Raw materials to production .
 Review and approve daily test results for materials.
 Schedule laboratory teams to ensure timely and accurate laboratory testing.
 Ensures compliance to the set specifications and takes actions upon
non compliance.
 Investigates and confirms OOS test results with lab. Analyst according
to the approved OOS SOP before reporting to the laboratory manager.
 Validate results and Approve new raw materials, or current materials
from new suppliers according to the material approval SOP and the
approved specifications.
 Performing Supplier qualification program through audits .
 Monitors and ensures that laboratories equipment’s calibration plan is fulfilled.
 Plan / Monitor laboratories requirements (Reagents, chemicals, media , tools ,
equipment ,…) and ensure that they are provided in a timely manner.
 Ensure good storage for raw materials retained samples in a secured
proper manner for monitoring , testing and traceability purposes .
 February 2009 - Present:
Analytical & Technical responsible of ISO 17025 team.
( European Egyptian Pharmaceutical Industry (Pharco Corporation))
Responsible for :
All ISO. technical affairs (raw materials and finished products ):
 Issuing & application of Standards Operating Procedures for all ISO activities.
 Supervising analysts work.
 Insuring results reproducibility .
 Uncertainty calculation .
 Participating in Proficiency testing lab. activities.
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2. (Previous work experiences)
- ( October 2010 to September 2014 )
Quality Control Senior (Raw materials analysis affairs )
(European Egyptian Pharmaceutical Industry(Pharco Corporation)).
Responsible for:
• Supervising Analysis affairs .
• Approval of raw materials for Production use .
• Issuing & application of Standards Operating Procedures (analysis affairs)
• Ensure that testing processes and Raw materials specifications are met &
taking corrective & preventive actions whenever needed & managing positive
release of Raw materials to production .
• Review and approve daily test results for materials.
• Supplier qualification program through performing GMP audits for raw materials suppliers.
(In China & India through May 2011)(In Malaysia , Penang island through February 2014).
- ( October 2004 to September 2010 )
Quality Control Specialist (Raw materials analysis affairs )
(European Egyptian Pharmaceutical Industry(Pharco Corporation)).
Responsible for :
 Complete analysis of raw materials against their monographs in pharmacopoeias.
 Dealing with all types pharmacopoeias such as :European , USP, British ,
International & Japanese ,through all their monographs, procedures, preparations
& general chapters.
 Dealing with all kinds of problems in analysis & source of errors , good thinking
about them to ensure quality.
 Member of ISO 17025 team of European Egyptian Pharmaceutical Industry
(Pharco Cooperation) (analysis affairs ).
 Applying GLP rules in the lab.
 Dealing with all kinds of testing through wet bench technique & applying
the following analytical methods:
1- Quantitative & qualitative analysis dealing with:
- Spectrophotometer such as (Shimadzu UV 2450) and (Cary 100Bio ) .
- IR spectrophotometer (Shimadzu FTIR 8200 ).
- NIR spectrophotometer ( Brucker ).
2- Chromatographic analysis dealing with
- HPLC such as :
 HP Agilent 1100 series ( Isocratic & gradient ones )
 Shimadzu .
- TLC technique .
3- Physical analysis dealing with:
- pH meter ( MP230 Mettler Toledo ).
- Balances ( Sartorius & Mettler Toledo )
- Refractometer ( OPTICH ).
- Polarimeter ( ADP220 ).
- Dissolution apparatus ( ERWEKA DT800, Hanson SR8 Plus ).
- Electrothermal apparatus .
- Potentiometer & Karl Fishcer techniques ( Metrohm ) .
- Particle size analyzer ( Mastersizer E 2000 , Malvern ).
- (October 2004 - July 2006)
Fully Responsible Pharmacist in Dr . Mohammed Motaewa
Pharmacy.( Ganaklese )
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3. Courses ,
job related experience , Certificates & Projects
Training courses:-
 TQM & ISO9001:2008 Course (Brooklyn Academy) (36 hours).
 Green six sigma / Lean Course - Minitab 17 (Brooklyn Academy) (72 hours).
 Project Management Professional(PMP-PMBOK V.5)(NEW HORIZONS)(40 hours).
 Attendance of USP conferences 2008 & 2012 in Cairo . 
 Application of ISO17025:2005 by EGAC .
 Advanced Quality Auditing Program ( ISO 9001 : 2008 ) - 15 days .
 FT-IR spectrometer (NIR -MPA) & OPUS LAB software / BRUKER - 5 days .
 Role of Certified reference materials in Method Validation in Chemical analysis /
National Institute of standards (NIS) - 3 days .
 End user Security - Revalidation Plan (Software validation)(according to MHRA).
 Training of trainer (TOT) - 6 days .
 FDA / WHO Inspections - 2 days .
 Statistic & Chemometrics for Analytical Method Validation - 8 days .
 Corrective / Preventive Actions (CAPA analysis) .
 Statistical Process Control (SPC) - 7 days .
 Application of USP standard in analysis.
 Particle size analysis by Malvern/Mastersizer 2000(Hydro MU unit &
Scirocco M dry unit) .
 Chromatographic separation techniques (TLC,GC, HPLC , …)
 Qualitative and quantitative analysis.
 c.GMP & its applications .
 Good documentation practice (GDP)/Documentation Pharmaceutical in Industry.
 Good Storage Practice (GSP) .
 Team leading and management skills.
 Time management .
 Gas Chromatography principles, strategies and applications(troubleshooting)-3 days.
 HPLC & its troubleshooting - 3 days .
 Determination of the expiration date of chemical solutions .
 Infrared Spectroscopy (FT-IR / Mid region ) & its applications .
 Atomic Absorption Spectrophotometric analysis .
 Functional Groups analysis (Basics of Organic & inorganic Chemistry ).
Job related experience:-
 Participating successfully in 7 field inspections by EGAC for ISO 17025
four as one of analysis team & three as Technical responsible
 Contributing successfully in proficiency testing lab. activities for 5 rounds
( UV analysis , HPLC analysis , TLC analysis )
 Operation and calibration of laboratories instruments and Apparatus;-
Analytical Balances, Muffles , water baths , Ovens , Vaccum ovens, Ph meters , Viscometers ,
Thermometers , Refractometer , Polarimeter , Electrothermal apparatus Infrared Spectrophotometer , NIR
Spectrophotometer, Ultraviolet Spectrophotometer , Potentiometer, Karl Fisher apparatus .
 Dealing with all Chromatographic systems and Techniques .
( TLC , HPTLC ,HPLC , GC )
 Dealing with & application of pharmacopoeial monographs and General
Chapters on raw materials analysis and required reagents and standards
preparations . ( European , USP , Chinese , international , …)
 Usage, Ordering and Storage of Chemical reference standards .

 Preparation, usage & storage of working standards .

 Dealing with awareness with WHO , ICH & FDA , Eudralex ,EMEA , OMCL &
ISO 17025 regulations.
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4. Certificates:-
 Total Quality Management (TQM-P):
-Source : Brooklyn Academy .
 Certified Six Sigma Green Belt (CSSGB)(DMAIC):
- Source : International Quality Federation (IQF) - USA / Certificate no.: AA11796
Link : http://iqf.org/?page_id=143
 Lean Six Sigma Green Belt (LSSGB):
- Source : Brooklyn Academy .
 Project Management Professional (PMP-PMBOK V.5):
- Source : NEW HORIZONS Computer Learning Centers .
Projects:
1 • May 2011
Supplier qualification program & performing GMP audits for raw materials suppliers
through team,(In China(API)...Biocause Ltd.....China associate Ltd....& India(API)....
Dr.Reddy's...Aarti drugs Ltd.....through May 2011).
2 • February 2014
Supplier qualification program & performing GMP audits for raw materials suppliers
through team,(In Malaysia,Penang island through February 2014-
Symbiotica Ltd. API manufacturer).
3 • February 2009
ISO 17025 Project (Accredited by EGAC , ISO17025:2005 ) for Assay &
Related substances of Ciprofloxacin Hydrochloride(USP)(HPLC).
4 • February 2009
ISO 17025 Project (Accredited by EGAC , ISO17025:2005 ) for Assay of
Prednisolone Sodium phosphate (European Pharmacop.)(UV).
5 • March 2011
ISO 17025 Project (Accredited by EGAC , ISO17025:2005 ) for Related substances
of Prednisolone Sodium phosphate (European Pharmacop.)(HPLC).
Languages
Personal Skills
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Computer Skills
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Interests
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 Arabic (mother tongue)
 English (Fluent written and spoken)
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 High communication skills.
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racle.
 Windows package (Windows & Microsoft Office).
 Internet search & navigation .
Cobol.
 Minitab 17 .
Reading.
Internet surfing & navigation.
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5. Personal
Information
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 Marital status: Married
 Nationality: Egyptian
 Date of Birth: 01/11/1982
Military service: Final exempt.
Driving license: Valid.
 Governmental service: Exempt .
 Place of birth: Saudi Arabia (Jeddah).
 Web Links : Linkedin :
https://www.linkedin.com/in/ahmed-adel-bsc-tqm-p-cssgb-iqf-6a4a7675?
trk=hp-identity-name
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