Mohamed Ghandour

Mohamed Elghandour
Profile
Production Specialist with a wide range of experience in the pharmaceutical industry. Able to work on own initiative
and as part of a team. Proven leadership skills involving managing, developing and motivating teams to achieve their
objectives. First-class analytical, design and problem-solving skills. Dedicated to maintaininghigh
quality standards.
Objectives
I am looking for a managerial challenging position with major reputable and esteemed company, which will provide
me with most of these opportunities and hopefully benefit from my long experience in pharmaceutical or other similar
field
Scholastics
-B.Sc. degree in Pharmaceutical Science, in June 2007, from Al-Azhar University -Cairo Egypt.
-Valid DHA (UAE) license.

WORK EXPERIENCE
1- March 2016 – Present
Ministry of Health and Population-Egypt

Department: Drug Stores Department (Directorate of Health Affairs in Kafr El-Sheikh)
Position: Pharmacist in charge
Job Description:
1- Managing and responsible for maintaining, receiving, warehousing, and distribution operations
by planning, coordinating to aid and improve operational performance and keep warehouse stand
by for any inspection.
2- Apply GSP (Good Storage Practice) and GDP (Good Distribution Practice) and maintain daily
operating schedules to ensure deliverables are met fully
3- Implementing of FIFO and FEFO removal strategies.
4- Manage the inbound and the outbound processes to achieve the shipment schedule on time.
5- Ensure the smooth running of the work steps by solving all the problems which can delay the
work and achieve all the store activities on time.
6- Confirm the implementing of the safety instruction for all the activities in the warehouse by all
the warehouse team.
2- Jan 2014 – Feb 2016
JULPHAR (Gulf Pharmaceutical Industries)
Department: Quality Control Department (Microbiology Section)
Position: Microbiologist
Job Description:
1- Microbiological analysis of bulk and finished products.
2- Microbiological sterility test for sterile raw material and finished products.
3- Microbiological analysis of water (water for injection, De-ionized water and RO water).
4- Determination of endotoxin in raw material, injectables and water by LAL test 5- Determination of particulate
matter in injectables.
5- Environmental monitoring of sterile production area.

3- Jan 2012 – Dec 2013
Department: Quality Control Department (Chemical Section)
Position: Chemical Analyst
Job Description:
1- Approve or reject raw materials with respect to quality standards and record supplier performance
2- Working on special projects applied on HPLC, UV and NIR for analysis of drugs in biological
fluids.
3- Demostrate excellent practical and theoretical knowledge instrumental techniques.
4- Collaborate with PDL, QA, Production and regulatory affairs in order to gather the relevant
information required for the product submission to the different health authorities
4- Oct 2008 – Dec 2011
Department: Production Department
Position: (Aseptic fill finish-Sterile formulation)
Job Description:
1- Responsible for Preparation, filtration and filling of injectable sterile products (Ampules,
Vials and Lyophilization Freeze dryer vials and Hormones vials).
2- Aseptic & Terminal Filling supervising for products like :Ampoules of Clofen,3V,Rantag
,mikacin,gental,cyonvit,premosan,scopinal,salurin,chlorohistol,histaloc & vials of Epotin,
Jusline & risk.
3- Ensure compliance of cGMP and safety requirements.
4- Managing the shifts and arranging the job description of assistant pharmacists, pharmacists
and skilled operators.
5- SAP software executive in the flow of production process orders and management facility.
6- To execute the production plan smoothly.
7- Reporting to high management as a kind of crisis management techniques.
8- Compensation and benefits to create attractive image and harmony in the production work
field.
9- Demonstrated ability to work independently and exercise sound judgment and problem
solving skills
10- Participates in factory wide internal audits and face international Audits (Merck, Saudi
FDA ).
11- Manages the implementation of the QMS (Quality Management System) to ensure
compliance with global standards and maintains current manufacturing trends and investigates
any potential problems.
▪ Training
▪ GMP courses
▪ GLP courses
▪ SAP courses
US FDA, Unicef, UAE.MOH, J.FDA, S.FDA, Egypt MOH, and Iraq. MOH
CONTACT.
Address: Cairo-Egypt
Telephone: 01099469101
Marital Status: Married
Gender: male
Citizenship: Egyptian
Birthday: 18 June 1984
Email: mohamedelghandour10@gmail.com
1- Dr. Sherif Hussien

Head of Quality Control - Gulf Pharmaceutical Industry (JULPHAR).
Telephone. 00201033969169
2- Dr. Kamal lymona

Assistant Director of Stores Department at the Directorate of Health Affairs in Kafr El-Sheikh
Telephone. 00201060054024

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Mohamed Ghandour

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Mohamed Elghandour

-Valid DHA (UAE) license.

1- March 2016 – Present

Ministry of Health and Population-Egypt

Position: Pharmacist in charge

3- Implementing of FIFO and FEFO removal strategies.

2- Jan 2014 – Feb 2016

JULPHAR (Gulf Pharmaceutical Industries)

Department: Quality Control Department (Microbiology Section)

1- Microbiological analysis of bulk and finished products.

5- Environmental monitoring of sterile production area.

JULPHAR (Gulf Pharmaceutical Industries)

Department: Quality Control Department (Chemical Section)

Position: Chemical Analyst

3- Demostrate excellent practical and theoretical knowledge instrumental techniques.

JULPHAR (Gulf Pharmaceutical Industries)

Department: Production Department

Position: (Aseptic fill finish-Sterile formulation)

1- Dr. Sherif Hussien

2- Dr. Kamal lymona

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