Basic Info

Mohamed Matter

More than 15 years

Egypt

Bachelor's Degree

Manager

Work Experience

Plant Manager at Delta Pharma

Experience Details

Plant Manager

Pharmaceutical

Manager

• overseeing the production process, drawing up a production schedule;
• ensuring that the production is cost effective;
• making sure that products are produced on time and are of good quality;
• working out the human and material resources needed;
• drafting a timescale for the job;
• estimating costs and setting the quality standards;
• monitoring the production processes and adjusting schedules as needed;
• being responsible for the selection and maintenance of equipment;
• monitoring product standards and implementing quality-control programmes;
• liaising among different departments, e.g. suppliers, managers;
• working with managers to implement the company's policies and goals;
• ensuring that health and safety guidelines are followed;
• supervising and motivating a team of workers;
• reviewing worker performance;
• identifying training needs.


Company Details

Delta Pharma

Cairo, Egypt

501-1000 employees

Manufacturing, Pharmaceuticals

www.deltapharmaegypt.com

Apr 2012 to present (5 years 9 months)
Quality Manager at Al debeiky Pharma

Experience Details

Quality Manager

Quality

Manager

• liaising among different departments, e.g. suppliers, managers;
• working with managers to implement the company's policies and goals
• overseeing the production process, drawing up a production schedule;
• ensuring that the production is cost effective;
• responsible for establishing the Quality Assurance / control systems, including designing of the Validation & Qualification programs,
• heading the Quality Control functions to direct QC operations & analytical method validations
• guiding the Qualifications / Validation Protocols & Reports preparation, Change Control documentation, Specs & OOS documentation, Market complaints handling, Deviation reports investigation & approvals and Stability studies programs
• Coordinating with Research for new product developments & analytical method Validations as per process / regulatory requirements,
• Handling Regulatory agencies visits and External customer visits / audits abroad
• Established the Quality Assurance / control systems,
• Designed the Validation Master Plan & all Validation protocols / schedules as well as Equipment Qualification protocols / schedules
• Supervising approval & release of the Non-sterile Dosage Form batches production
• Review and approval of Qualifications / Validation Protocols & Reports, Change Control documents, Specs & OOS documentation, Market complaints handling, Deviation reports investigation & approvals
• Review and approval of Stability studies data for shelf life determinations


Company Details

Al debeiky Pharma

Cairo, Egypt

501-1000 employees

Manufacturing, Pharmaceuticals

www.dbk-eg.com

May 2007 to Mar 2012 (4 years 10 months)
QA Section Head at MEPACO

Experience Details

QA Section Head

Quality

Manager

• Head of QA department,/ Validation Section involving production of Tablets, capsules, , Liquids,
• Established the Quality Assurance systems,
• Designed the Validation Master Plan & all Validation protocols / schedules as well as Equipment Qualification protocols / schedules
• Review and approval of Qualifications / Validation Protocols & Reports, Change Control documents, Specs & OOS documentation, Market complaints handling, Deviation reports investigation & approvals


Company Details

MEPACO

Sharqia, Egypt

501-1000 employees

Manufacturing, Pharmaceuticals

N/A

May 2004 to Apr 2007 (2 years 11 months)
Quality Section Head at Global Napi for Pharmaceutical ( GNP )

Experience Details

Quality Section Head

Quality

Manager

• Follow the work of analysis of all activity in the Qc lab.
• Supervise and follow the validation project of Merck sharp products manufactured by GNP company (Vioxx, singulair and zocor tablets )
• Approve or reject the released documentation of raw materials and products after their analysis.
• Supervise and follow the work of analysis of raw materials, packaging materials, bulk and finished products and insure the verification of approved specification.
• Assist the plan work through the lab. To precisely follow the production schedules and adhere to the lead times agreed.
• Coordinate with other departments ( production , quality assurance , planning and purchasing departments) for control of the company total quality policy through the application of the GMP rules
• Developing new methods of analysis for new products.
• Preparation and updating the specification of raw materials , packaging materials and finished products


Company Details

Global Napi for Pharmaceutical ( GNP )

Giza, Egypt

501-1000 employees

Manufacturing, Pharmaceuticals

N/A

Oct 2001 to Apr 2004 (2 years 6 months)
Quality Supervisor at Alkan / Lilly Egypt Pharmaceutical

Experience Details

Quality Supervisor

Quality

Manager

• Preparation of standard operating procedure dedicating to the operation and calibration of all lab. Instruments, All quality procedures concerning all departments including QA, Warehouse ,Engineering ,Administration , …etc
• Check and participate in the investigation of all product complaints related to chemical and microbiological tests of the active materials
• assisted as an quality & environmental internal auditor in the company
• Supervise and follow the work of analysis of raw materials, packaging materials, bulk and finished products and insure the verification of approved specification.
• Training the QA/QC personnel in the specialized analytical areas.
• Reviewing QA/QC and Plant Documentation for adequacy for filing of Drug Master Files



Company Details

Alkan / Lilly Egypt Pharmaceutical

Giza, Egypt

501-1000 employees

Manufacturing, Pharmaceuticals

N/A

Dec 1999 to Sep 2001 (1 year 9 months)
Research and Quality Specialist at EIPICO FOR PHARMACEUTICAL

Experience Details

Research and Quality Specialist

Quality

Experienced (Non-Manager)

• Developing new methods of analysis for new products.
• Preparation and updating the specification of raw materials , packaging materials and finished products
• Preparation of standard operating procedure dedicating to the operation and calibration of all lab. Instruments, All quality procedures concerning all departments including QA, Warehouse ,Engineering ,Administration , …etc
• Check and participate in the investigation of all product complaints related to chemical and microbiological tests of the active materials
• Perform & Follow the work of analysis of all activity in the Qc lab


Company Details

EIPICO FOR PHARMACEUTICAL

Cairo, Egypt

More than 1000 employees

Manufacturing, Pharmaceuticals

N/A

Sep 1992 to Oct 1999 (7 years 1 month)

Education

B.SC Science. (Chemistry) in Chemistry

Education Details

B.SC Science. (Chemistry)

Chemistry

Zagazig University, Egypt

C / Good / 65 - 75%

Chemistry Physics Math. Boteny

N/A

Zagazig University
1986 - 1989
High School - Thanaweya Amma

High School Details

Thanaweya Amma

abouhamad sec. school

Egypt

1985

B / Very Good / 75 - 85%

N/A

abouhamad sec. school
1985

Training and Courses

Training/Course Details

Mini MBA

Dec 2014

Knowledge Trees

• Attended course of Mini MBA by Knowledge Trees Company including:- Strategic management ( 2 sessions) Professional and soft skills ( 4 sessions) HR ( 4 sessions) Finance managment ( 3 sessions) Project management ( 5 sessions)

Training/Course Details

Performance management system

Feb 2015

Levarage

N/A

Training/Course Details

Axepta 2012 microsoft ERP system

Apr 2013

Bayanat Co.

N/A

Jobseeker photo

Profile Skills and Keywords

Axepta 2012 Microsoft ERP SystemChallangeChemistryManagmentManufacturingMini MBAPerformance Management SystemPharmaceuticalPharmaceutical ManufacturingPharmaceuticalsPlant ManagerQA Section HeadQualityQuality AssuranceQuality ControlQuality ManagerQuality Section HeadQuality SupervisorResearch And Quality SpecialistSuccessSupport OthersTeam Work

Self-assesed Skills

Fields of Expertise

Quality

Quality

: Advanced

: High

:

More than 7 years

Managment

Managment

: Advanced

: High

:

More than 7 years

Pharmaceutical Manufacturing

Pharmaceutical Manufacturing

: Advanced

: High

:

5-7 years

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