1. C.V
Name : Abir Moustafa Kamal Al-Alfy.
Birth Date : 03-09-1973
Address : 130D –Hadayek El- Ahram,
Phone No : Mobile: (0100)1094930.01110533517
Social State : Married.
E-Mail : abiralfy@gmail.com, abiralfyz@yahoo.com
Qualifications: B.Sc. of Biochemistry, Faculty of Science, Ain Shams University,1994.
Previous Experiences:
From December 2015 until now as a Q.C & Production manager at Centra for medical
supplies
From January 2013 until December as a Q.C manager at pharomedica for medical device
industries
From September 2010 until December 2012 as production assistant manager at City
Pharma company for veterinary pharmaceuticals
From November 2004 until September2008 as a QA assistant manager at Medco Erp LTD
Holland Company for veterinary pharmaceuticals.
From November 2002 until October 2004 as a deputy production manager at Medco Erp
LTD Holland company for veterinary pharmaceuticals.
From July 1997 until October 2002 as a dialyzer production manager at Haidylena for
advanced medical industries.
From July 1995 until June 1997 as a dialyzer production supervisor at Haidylena for
advanced medical industries.
From November 1994 until June 1995 as a IPC at Haidylena for advanced medical
industries.
Practical Experiences:
Able to perform all production activities. (Follow up all production steps in manufacturing
area, follow up any activities done in gowning area &production area and packaging area
& follow up the batch record)
Able to create the entire SOP related to the production activities (processing, packaging,
equipment,...).
checking the packaging materials (boxes, leaflet...)
Able to analyze al! the raw material and the finished products.
Able to perform all instrumental QC activities (operation of the spectrophotometer, pH
meter, viscometer, analytical balances, melting point...).
Able to perform all QA supervisor activities. (Creation and renew SOP'S for all
department of company, follow up the internal and external calibration, follow up the
system work in warehouse, follow up the checklist record in production ,stores, etc..,
follow up the IPC activities, follow up the internal audit done by the QA manager and the
external audit done by customer supplier and MOH, training the new Q.A. inspector
Able to implement all cGMP, GHP and GLP rules.
Able to preparation media
Able to perform all microbial test (bioburden) sterility test , microbial count in clean room
, count of the operators finger print ., microbial count of operator coat ) .
Additional Skills:
Fluent in English language (written and spoken).
Familiar with computer languages (Word, Excel, Power Point,...).
