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Curriculum Vitae
Ahmed Mohammed Ali Ali
15 –Salman El Farase st, Obour city, Egypt.
Home phone: 22627015
Mobile phone(1): 01222714537
Mobile phone(2): 01272052220
E-mail: DrAhmedAlii@hotmail.com
E-mail: Ahmed.Ali@Loreal.com
Career Objective:
Seeking a challenging career within a Struggling & creative team focusing to make a continuous
process of improvement whereby my skills could be fully utilized & developed.
Education:
Bachelor degree in pharmaceutical science, Helwan University(class of 2004).
Overall grade: Very good with honor.
High School: Nasr City School, July 1999.
Work Experience:
L'Oreal cosmetic industry.
Subcontracting cell leader
July 2015 –Current
*Duties:
-Validate the subcontracting production plan.
-Sequence the production plan and follow with the subcontractors its execution.
-Define and provide subcontractor capacity parameters to the Master Scheduler.
-Check that the production plan matches the subcontractor's capacities.
-Coordinate the physical flows between the plant and the subcontractors: release the resources
(packaging components, bulk, etc.) required to fulfill the production plan.
-Participate in selecting the plant's subcontractors with Purchasing and own the contracts that
the plant signs with the subcontractors.
-Coordinate subcontractor industrial feasibility tests.
-Facilitate resolution and improvement of quality issues at subcontractors.
-Define and manage subcontractor working methods.
-Coordinate the elaboration of administrative documents (quality, ETNSHE, etc.): circulate and
track them.
-Ensure that the subcontractor respects L’Oreal ETNSHE and L’Oreal Quality rules and legal
obligations.
-Track subcontractors' stocks and ensure the accuracy of inventories.
-Monitor the subcontractor supply chain performance (service and costs).
-Coordinate with Purchasing and maintain the necessary data definition in the plant IT systems.
L'Oreal cosmetic industry.
Toll manufacturing supervisor
May 2014 –June 2015
*Duties:
-Giving a condensed GMP training to the shop floor employees & their supervisors.

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-Supervising Loreal Egypt subcontractors.
-Setting the layouts of working areas.
-Coordinate with the subcontractors to improve the receiving, sorting, manufacturing, packaging,
testing, documentation & shipment process to fulfill the Loreal quality requirements.
-transfer the basics of quality knowledge to subcontractors who are new in the co-packing field,
doing very close supervision to ensure that they are following the quality guidelines.
-Creating & improving KPIs of subcontractors.
-Coordinate with supply chain department to achieve the required plan.
L'Oreal cosmetic industry.
July 2013 –April 2014
Quality control supervisor “task force”
-Responsible for
Managing all activities in the lab:
Packaging, micro, raw material, bulk & finish product testing lab.
Examples of these activities:
-Managing 3 shifts for 6 days per week.
-Setting the year objectives for analysts to achieve the department goals.
-Saving the Laboratory’s overheads requirements.
-Preparation of the continuous new launches.
-Continuous troubleshooting at the startup phase.
-Building a work flow system starting from receiving the samples till taking the final decision.
-Internal, external calibration & maintenance of the testing devices.
-Implement & Maintain GLP & 5s.
-Hiring new analysts & technicians & ensuring that they get the required safety & technical training.
-Creating operation, calibration & cleaning SOPs for lab devices.
-identifying the Standard working time per every test to meet the planning expectations & to
facilitate the managing process.
-Managing the lab waste disposal.
-working with the production, planning team to settle a process flow to simplify the Communication.
-End year review (appraisal) for analysts.
L'Oreal cosmetic industry.
Toll manufacturing supervisor
Apr 2013 –July 2013
GlaxoSmithKline, Egypt.
November’ 2008- March 2013
Quality Assurance Officer
-Responsible for the following areas:
 Soft gelatin area(manufacturing & packaging) from 11/2008 to mid of 2009.
 Semisolids area(manufacturing & packaging) in addition to Syrup area & Soft gelatin area from
mid of 2009 to nearly end of 2010.
 Warehouse & dispensing from end of October to Jan/2011.
 Solid area (manufacturing & packaging) from Jan/2011 to end of the year.
 Solid processing area since Jan/2012.
During these periods my duties were the following:

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Assuring the implementation of cGMP rules through area monitoring.
Internal auditing through L1 audit.
Assuring the implementation of validation plans for both process validation and cleaning
validation.
Ensuring optimization of processes and projects to reach desired efficiency level to meet
required standards.
Responsible for the revision of the production B.R before release to the market.
Creating and reviewing SOPs, batch records, bill of materials and product specifications.
Managing the products complaints, OOSs and the process deviations.
Responsible for the calibration check of IPC equipments.
Raising and approving any change as per its relation to the area under my supervision to assure
that implementation of the change is under control and complies with GMP standards.
Reviewing & approving the Engineering calibration reports of the devices in any area under my
supervision.
Reviewing & approving the Validation protocols (URS,IQ,OQ,PQ, initial validation &device
assessment)
GlaxoSmithKline, Egypt.
May’ 2006- October’ 2008
Quality control analyst
 Duties:
 Responsible for the stability stores (receiving samples from Q.A, entering and withdrawing
samples from the stores).
 Responsible for the laboratory balances ( calibration ,weekly check and troubleshooting).
 Participation in the internal audit execution, reporting, and following up closure of the
recommendation.
 Analysis of all finished dosage forms using HPLC, UV, dissolution, disintegration tester.
 Assisting in creating new methods of analysis to facilitate the analysis process.
 Training for the newly hired analysts.
* Assisting in managing the stability section.
* Calibration of HPLC.
SCHERING-PLOUGH Company
July 2005 till May 2006
 Duties:
 Working as a medical representative in El-mohandisin city.
EPCI Company
Feb 2005 till July 2005
 Duties:
 Working as a medical representative in Heliopolis & Nasr city.
Cairo medical center pharmacy
July 2004 till Feb 2005
 Duties:
 Dispensing both inpatient & outpatient prescriptions.
 Purchasing & following up the stock through dealing with the pharmaceutical distribution companies.

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Computer, Languages and Interpersonal Skills:
 Excellent command of English language.
 Business, quality & time oriented.
 Put my customer at the heart of every decision.
 High sense of urgency.
 Excellent communication skills implemented to overcome the working environment bureaucracy.
 Building excellent & trustful relationship with my colleagues.
 Enjoy working in a new environment with a new collaborative staff.
 Hard worker.
 Flexible thinking.
 Continuous identifying ways to improve & simplify things.
 High desire for changing working environment to the better.
 Familiar with Good Manufacturing& Laboratory Practices.
 Very good knowledge of Microsoft Office applications.
Achievement
*The analyst of the month 4 times within one year.
*Outstanding evaluation for 2 times, once in the lab & the other in the quality assurance.
Personal Information: Date of Birth: 12/2/1982.
Place of Birth: Cairo, Egypt.
Nationality: Egyptian.
Marital Status: Married.
Military Service: Exempted.
Driving license: available & private car.
Interests: Playing soccer, Swimming, Travelling & friendly Discussion
References Furnished upon Request