1. Current Job: QC Manager in Western Pharmaceutical Industries
Mobile: 01287170717
C.V of Mohamed Shawky Page I of 8
C.V.
Mohamed Shawky Ahmed
Block 18082-zone 1, District 9 - Oboor, Egypt
Mobile: 01287170717
E-mail: Mohamedshawky160@hotmail.com
Dear HR Manager:
You will be happy for the prospect of recruiting a person that is a high-
performer, well-qualified and professional for a position : QC Manager in the
pharmaceutical industry.
As you can see in my enclosed resume, I have more than 12 years solid,
successful experience with three companies in all QC activites including QC
analysis of finished and raw materials also Stability and methodology and
finally R&D activites, receiving numerous promotions due to my excellent
performance. I believe you will be able to see that I have gained exceptional
skills during my previous experience. If you have any questions or wish to
arrange an interview, please call me at 010287170717.
Thank you for your consideration and time.
Yours truly,
MOHAMED SHAWKY

2. Current Job: QC Manager in Western Pharmaceutical Industries
Mobile: 01287170717
C.V of Mohamed Shawky Page II of 8
Personal Data :
Name : Mohamed Shawky Ahmed
Date Of Birth : 01/05/1980
Nationality: Egyptian
Marital Status : Married
Military Record : Exempted
Address : Block 18082-zone 1, District 9 - Oboor, Egypt
Mobile No. : 01287170717 01287170717
Objective:
 Seeking a challenging position in a well-known organization where I can enhance
and develop my interpersonal skills.
 I am confident in my ability to help you to translate your creative ideas into
ground breaking methods and processes.
 I have the ability to adopt and adapt the necessary problem solving tools to meet
any challenges or problems faced.
Being a performance driven and forward thinking personality, I deeply welcome the
oppourtunity to meet with you to discuss my eligibility in order to be a member within
your team and how my skills would benefit your company
Education & Degrees :
1996- May 2001 Bachelor Degree of pharmacy Ain Shams University
Grade : Very Good

3. Current Job: QC Manager in Western Pharmaceutical Industries
Mobile: 01287170717
C.V of Mohamed Shawky Page III of 8
SKILLS
Language skills :
 Fluent in both spoken and written Arabic.
 Fair in German
 Very Good command in both spoken and written English.
Computer skills :
 Software: Microsoft office 2000, Word & Excel
 Operating System: Microsoft Windows 7/VISTA/95/98/2000/NT/XP, MS-DOS
 Miscellaneous: Internet Surfing
 New computer certificates: visual basic 6 from Microsoft
Personal skills :
 Leadership skills including recognizing the strengths and weaknesses in others
 Enthusiasm...high level of motivation (self motivated).
 Willing to perform additional activities outside own area of expertise.
 Hard worker and have the ability to work under pressure.
 Decisive, able to escalate response to situations when relevant.
Training Courses:-
October 2007  MQM master in quality management in P&Q institute (Arab
academy for science and technology)
August 2010  CQM in MATEC center for training and consultancy by IMS
July 2010  Internal quality auditing in MATEC center for training and
consultancy by IMS
June 2010  Six sigma in MATEC center for training and consultancy by IMS
October 2013  TQM certificate from P&Q institute (Arab academy for science
and technology)

4. Current Job: QC Manager in Western Pharmaceutical Industries
Mobile: 01287170717
C.V of Mohamed Shawky Page IV of 8
Current position:-
Western pharmaceuticals:
Job Description as QC Manager: From 1/6/2014 till now
 General
1- Responsible for maintaining the quality and reliability of the products.
Setting quality objectives for the QC department and evaluation according to the key
performance indicators.
2- Application of all GLP concepts in all activities of Western Labs.
3- Estimation for the annual budget for the quality departments.
4- Conduction of regular training programs for improving the performance of the QC
analysts and on job training for the freshly joined subordinates.
5- Responsible for investigation of any non conformity results, handling of laboratory
variations and conducting the appropriate corrective action and preventive action.
Preparation of action plan and weekly reports.
6- A successful management of the QC resources to maintain the quality and
reliability of Western's products for eight successive. years.
7- Up to standard establishment of Western 's QC department premises, instruments
quality system plans, SOPs, MoAs, specifications,
8- Performing and following up the QC Department development plan [cost against
benefit]
 QC chemical & microbiological labs :
9- Ensure that necessary and relevant tests are actually carried out and that
materials are not released for use, nor products released for sale or supply, until
their quality has been judged to be satisfactory.
10- Managing the chemical and microbiological analysis of environmental
monitor raw materials, packaging materials and finished products according to the
recent official Pharmacopoeia, within a preset reasonable time.

5. Current Job: QC Manager in Western Pharmaceutical Industries
Mobile: 01287170717
C.V of Mohamed Shawky Page V of 8
11- Responsibility for follow up analysis of finished products.
12- Certification of confirmed data.
13- Follow up the due time for validation and calibration of lab equipments.
14- Following the documentation required for controlling the responsibilities
sops (standard operation procedures) and to comply the requirement of GMP and
ISO9000 systems.
15- Follow up and performing the on job training plan in Quality control
department
16- controlling and following up the IPC – department with all responsibilities of
testing out all steps of product production
17- Responsible for application of cleaning validation protocol and s process validation
[by reviewing and approving the protocols to be applied and confirming the result
data]
18- Responsible with QA Manager to prepare and review all data concerned with
MOH visits [food supplement – pharmaceutical …….. etc]
19- Following up the microbiology department and processing the work plan and
designing the department strategy
 Stability & Methodology lab:
20- Ensure that method of analysis for newly established products are valid according
to ICH guidelines.
21- Ensure that the stability study program is proceed according to the predesigned
plan either for accelerated stability or ongoing stability studies.
22- Reference for Designing new methods for analysis of new products. With full
items of analytical method validation of any product
23- Following up the preparation of an invitro study for drugs to analysis the amount
of invitro dissolution of the active material comparing with the original drug
registered in the FDA

6. Current Job: QC Manager in Western Pharmaceutical Industries
Mobile: 01287170717
C.V of Mohamed Shawky Page VI of 8
24- Responsibility for revision and confirming all stability study of the finished
products and products under registration (accelerated and long term stability
studies ……… as to insure the stability of the dugs (active material) and the formula
of the drugs is the suitable one for application)
25- Revision and approval of analytical method validation, product stability testing,
trend analysis for the chemical and microbiological testing.
26- Analysis experience for different types of samples water, raw materials, packaging
materials, stability,
3- Responsible for R&D Department (R&D)
27- Ensure that newly designed products in the pipeline passed by the normal
sequence till pass similarity study.
28- Check & approve all products manufacturing formulas and processing instructions
and ensure that batch records is complying with it.
29- Following up and evaluation of R&D department formulation of new drugs and
development of old products
Job Description as Assistant QC Manager: From 1/6/2006 till 01/06/2014
Job Description:
1- Responsibility for follow up analysis of finished products.
2- Responsible for all stability study of the finished products and products under
registration (accelerated and long term stability studies ……… as to insure the
stability of the dugs (active material) and the formula of the drugs is the
suitable one for application)
3- Certification of confirmed data.
4- Follow up the due time for validation and calibration of lab equipment.
5- Following the documentation required for controlling the responsibilities sops
(standard operation procedures) and to comply the requirement of GMP and
ISO9001 system.

7. Current Job: QC Manager in Western Pharmaceutical Industries
Mobile: 01287170717
C.V of Mohamed Shawky Page VII of 8
6- Designing new stability indicating methods for analysis of new products with full
items of analytical method validation
7- Follow up and performing the on job training plan in QC department.
8- Controlling and following up all IPC department activities concerning IPC tests
for all production steps.
9- Responsible for application of cleaning validation protocol and process
validation [by reviewing and approving the protocols to be applied and
confirming the result data]
10- Performing of all invitro studies for drugs to analysis the invitro dissolution of
the active material comparing with the original drug registered in the FDA
11- Responsible with QA Manager to prepare and review all data concerned with
MOH visits [food supplement – pharmaceutical …….. etc]
12- Following up the microbiology department and processing the work plan and
designing the department strategy
13- Performing and following up the QC Department development plan [cost
against benefit]
14- Formulation of new drugs and development of old products
15- Following up the toll products in different companies outside the company
JEDCO International Pharmaceutical Company: 01/06/2002-01/06/2006
Job Description as Finished Product Senior in QC Lab:
1- Supervision of production activity and raw material activity till finished product
delivery
2- Dealing with the instruments as HPLC, spectrophotometer, dissolution ……….etc.
3- Preparing of S.O.Ps for the cleaning, operating, calibrating and handling of
different instruments

8. Current Job: QC Manager in Western Pharmaceutical Industries
Mobile: 01287170717
C.V of Mohamed Shawky Page VIII of 8
4- Qualitative and quantitative analysis of different finished drugs released by the
company to ensure acquiring the characters in the method of analysis placed in each
drug file during and after drug production
5- Stability analysis of the finished products for company
ATOS Pharmaceutical Company:
Job Description as Analytical specialist in R&D Department: 01/10/2001-01/05/2002
1- Qualitative and quantitative analysis of different medicinal plants cultivated by the
company to ensure acquiring the high characters in the different pharmacopeias
such as the British and European pharmacopoeia
2- Qualitative and quantitative analysis of different drugs produced and released by
the company to produce a complete file of that drug to be registered in the
Egyptian ministry of health to have the permission in being produced in the market
3- Analytical research and developing new qualitative and quantitative analysis
methods for new medicinal plants or drugs working with professors from the Cairo
pharmaceutical university
References:
Will be available upon request.