exeutive director
wleedpack company
مجموع سنوات الخبرة :16 years, 3 أشهر
-Develop the organization's annual budget plan and allocate this budget
-Responsible for purchasing production machines to achieve the necessary quality,
productivity and increase profitability
-make production plan according to capacity of productivity to achieve customer request
-Creating job opportunities and setting administrative policies
-Establish and maintain good relationships with various department in organizations
-Reporting to the owner and working closely with it for decision-making
-Supervising and cooperating with the organization's staff members
-Developing and implementing strategic plans
-Supervising the organization's board of directors and its meetings
-Overseeing the marketing process and other communications efforts
-Reviewing and approving service contracts
-Responsible for all research and development of raw materials, product development
and new products according to customer requirements and marketing
-achieve customer needs&expectation
-implement lean and six sigma tools to make cost saving
-Coordinate and perform all vendor qualification and compliance audits.
-Perform lot release activities and insure proper delegation,
-issuing all compliance reports as per the Regulatory authority requirements.
-Provide oversight for Quality Control activities performed by testing laboratories and
manufacturing companies.
-Oversee investigations of all non-conformances (deviations, OOS).
-Ensure that GMP, GLP and GSP requirements and quality standards are recognized,
understood and maintained across the Company.
Implement six sigma black and lean systems to reduce (cost, defect cycle-time and waste)
-Improve all production line according to the requirements of food packaging,
Responsible for all research and development of raw materials, product development and new products according to customer requirements and marketing
achieve customer needs & expectation
implement lean and six sigma tools to make cost saving in all departments
Supervising all Quality Assurance & Quality Control responsibility with the following main objectives:
-Develop, implement, manage, audit and maintain quality systems
-Coordinate and perform all vendor qualification and compliance audits.
-Perform lot release activities and insure proper delegation,
-issuing all compliance reports as per the Regulatory authority requirements.
-Provide oversight for Quality Control activities performed by testing laboratories and manufacturing companies.
-Develop, manage and maintain ISO systems such as (ISO9001/2015-1SO22000/2005-BRC-17025-14001-18001-Yum).
-Oversee investigations of all non-conformances (deviations, OOS).
-Ensure that GMP, GLP and GSP requirements and quality standards are recognized, understood and maintained across the Company.
Implement six sigma black and lean systems to reduce (cost, defect cycle-time and waste)
-Improve all production line according to the requirements of food safety,
-Spokes persons to the relevant regulatory authority in situation need communication.
-Ensure in-process and finished products and processes conform to in-house policies and
procedures as well as other applicable regulations and guidelines.
-Budgetary and managerial responsibility for Quality Assurance and Quality Control.
-Work across all disciplines (e.g. manufacturing, Engineering, IT, etc.) to ensure that the Company maintains a state of readiness for inspection by regulatory agencies.
-Keep abreast of changes to quality regulations and guidelines, advising the management team of any business implications of these changes.
-Lead, manage and ensure proper training and its adequacy in case of any relevant change management programs throughout the company.
Supervising all Quality Assurance & Quality Control responsibility with the following
main objectives:
-Develop, implement, manage, audit and maintain quality systems
--Follow up and improve the performance of lab, IPC and create specification for raw /
packaging materials and finished product
-make validation of test method and stability studies for finished product
-Coordinate and perform all vendor qualification and compliance audits.
-Perform lot release activities and insure proper delegation,
-issuing all compliance reports as per the Regulatory authority requirements.
-Provide oversight for Quality Control activities performed by testing laboratories and
manufacturing companies.
-Develop, manage and maintain ISO systems such as (ISO9001/2015-1SO22000/2005).
-Oversee investigations of all non-conformances (deviations, OOS).
-Ensure that GMP, GLP and GSP requirements and quality standards are recognized, understood and maintained across the Company.
-Implement six sigma black and lean systems to reduce (cost, defect cycle-time and waste)
-Improve all production line according to the requirements of food safety,
-Spokes persons to the relevant regulatory authority in situation need communication
-Ensure in-process and finished products and processes conform to in-house policies and
procedures as well as other applicable regulations and guidelines.
-Budgetary and managerial responsibility for Quality Assurance and Quality Control.
-Work across all disciplines (e.g. manufacturing, Engineering, IT, etc.) to ensure that the
Company maintains a state of readiness for inspection by regulatory agencies.
-Keep abreast of changes to quality regulations and guidelines, advising the management team of any business implications of these changes.
-Lead, manage and ensure proper training and its adequacy in case of any relevant change
management programs throughout the company.
-Provide quality guidance to different company areas, projects and programs.
-Lead several Quality improvement initiatives in the company i.e Quality culture and first
path quality, ..etc
-Train and assure the GMP, GLP &GSP implementation
-Implement six sigma black and lean systems to reduce (cost, defect, cycle-time and waste)
-Manage and establish the issues of procedures and work instructions for the various departments of the company
-Follow-up preparation of the annual plan of internal audit for quality system .
-Follow-up quality objectives and Performance achieved (KPIs’) in various departments and sectors
- Ensure the Sustainability and effectiveness of the quality system
- Provide quality reports to board management and check further requirements for continuous development and improvement .
-Follow up and improve the performance of lab, IPC and create specification for raw /packaging materials and finished product
- Measuring and monitoring the efficiency and effectiveness of all processes for quality within the various departments
- Follow-up/quick responding to customer complaints then analyzing the results
- Supervise the implementation of a management review to fulfill the different quality systems
- managing the documentation process in accordance with the requirements of international standard ISO 9001/2000, ISO FSSC22000, ISO14001, 18001, BRC, Globle GAP, ISO 17025, BSCI, ISO22000
,
-Train and assure the GMP &GSP implementation
-Implement six sigma black and lean systems to reduce (cost, defect, cycle-time and waste)
-control of issues and establishment of Procedures and work instructions for the various departments of the company
-Follow-up operations of distribution of documents in force places of employment and supervision to withdraw canceled .
-Follow-up preparation of the annual plan of internal audit for quality system .
-Supervision of the internal audits and follow-up of non-compliance cases detected
-Follow-up quality objectives and Performance achieved (KPIs’) in various department and sectorss
- Ensure the Sustainability and effectiveness of the quality system
- Provide quality reports to top management and the requirements for continuous development and improvement .
- Maintain awareness of the importance of workers to meet the desires and needs of customers
- Measuring and monitoring the efficiency and effectiveness of processes for quality within the various departments
- Follow-up corrective actions to customer complaints and make analysis and record the results
- Supervise the implementation of a management review in different quality systems
- establish, preparation, maintenance and preservation on documents andthe quality management system in accordance with the requirements of international standard
ISO 9001/2000, ISO FSSC22000, ISO14001, ISO18001
Implement six sigma black and lean systems to reduce (cost, defect, cycle-time and waste )
Train and assure the GMP &GSP implementation
Reviewing standard specifications for raw materials and supplies
Reviewing the implementation of quality system in the suppliers place
Participate in approving new suppliers
Cooperate with marketing in order to design/ develop a product
Represent the company in external audit on suppliers
Determine the quality requirements when contracting the supplier
Weekly reports on problems of supply from the production line
follow up corrective actions record for the problems of supplies and make preventive action on it
Define the standard specifications for the packaging material and confirm their efficiency and whether it’s enough or not
Review and develop test method for packaging material
Provide technical support to rapidly solve any branch “outlet” complaints
follow up storage method of the raw materials and finished product
Monitor the implementation of ISO 9001/2008 in different Departments
Work hazard and risk assessment and reduced it
Develop the quality of product
Review of chemical, physical and Microbiology analysis to take the appropriate decision for the product launch
take samples of the finish product and compare it with the standard specification
Assistant project manager for ISO 17025/2005(General requirements for
the competence of testing and calibration laboratories)
, ISO 18001/2007(management systems for Occupational health and safety), 14001
(environmental protection), ISO9001/2008
in (Memphis pharmaceutical Company , CARAS (Bioequivalent lab)in
pharmacy Cairo university, Siver Egypt Powered Air Conditioners, GRC
(Bioequivalent lab), NILE pharmaceutical Company , NASR
Pharmaceutical Company, Soils, waters Environment Research Institute
Egyptian Research and Development Company, Arab Pharmaceutical company
, Arab company for electronic(Panasonic), CID
Pharmaceutical company, Cairo Pharmaceutical company
and NODCAR)
Working as analyst on HPLC and UV spectrophotometer
and make validation study for test method
Working as medical representative
make different project to make cost saving and improve performance of quality in: reduce rework by using six sigma tools reduce waste time of production filp off by using lean tools make ISO 17025:2017 project by using PMP tools Contemporary Management Quality Assurance Concepts & Systems . Statistics for Management Decisions Competing in Global Environment Quality Management Management Information Systems Statistical Quality Control Research Methodology Customer Relationship Management Group Dynamics Business Process Reengineering Advanced Topics in Quality Management PMP Six sigma lean management business continuity .