Address: 21 El Weehda El Arabia st., Mob: 012-02212622

Gesr El Suez Ain Shams, Cairo. Mob: 010-09164862

E- mail :

Peter Nagy Sheath

Objective Seekinga position through which, my academic background, personal skills and experience can be applied, developed and challenged.

Personal Data

Nationality:Egyptian

Place of birth:Cairo

Date of birth:22/12/1984

Marital Status:Married

Military Status :Exempted

Driving License: Valid

Passport: Valid

Education

  • 2005 - 2001 Ain-shams University

B.SC of Chemistry / Zoology from the faculty of science in 2005 with

Finalgrade: Good

  • Diploma in Total Quality Management TQM from AUC (from January 2008 to January 2009 Saturday only).

(Six sigma, ISO9001, 14001, Audit, planning for top quality, statistical quality control, project management, managing the quality functions)

Training

  1. Lead Auditor (OHSAS 18001:2007) registered from IRCA (BUREAU VERITAS) 12/2013
  2. Lead Auditor (ISO 9001-2008) registered from IRCA (BUREAU VERITAS) 11/2011
  3. Certified Manager of Quality / Organization Excellence (CQM) from American Society for Quality

Certification Number 13052 (November 2009)

  • Internal Audit training for Quality system ( ISO:9001)from engineering and quality experts (30/6/2008)
  • Certificate of completion Quality Control Circle Course (KAIZEN productivity QualityImprovement center –Ministry of trade & industry) Feb , 2009
  • Certification green belt of six sigma from Quality America INC (90 hours).

Experience

April 2014 till now:

Quality Assurance Manager at Univest group for cosmetics industries

Specific duties

  1. Develop, implement, communicate, follow up and maintain the Quality Health ,Safety and Environmental quality plans, Quality Systems ,Quality Objectives and Policies
  2. MaintainQuality achievement and performance improvement throughout the organization using statistical tools
  3. Ensuring the execution of corrective action and preventive action in QHSE and GMP
  4. Implement, Communicate and Follow the GMP requirements.
  5. Monitoring daily performance for QHSE and GMP by gathering relevant data and producing statistical reports.
  6. Conduct GMP training in a daily bases according to training plan.
  7. Setting up and maintaining controls and documentation procedures.
  8. Internal Auditor for GMP ISO 9001, 14001and OHSAS 18001 ,
  9. prepare for time meeting understand the requirements of other departments
  10. Implement, maintain and follow the management review and it’s outputs.
  11. Develop, implementand maintainAudit Check List in order to check on the various departments
  12. Prepare daily, monthly and yearly reports about the status of GMP, QHSE overall department contain an assessment and the needs for improvement
  13. Prepare the budget for QHSE department every year
  14. Conduct risk assessment in daily basis for every place and implement an action plans for every issue
  15. Conduct Job Safety Analysis for every activity and reviewed in daily basis
  16. Work with production in setting SOP, Batch Record and prepare IPC work instructions documents.
  17. Prepare calibration plan (External and Internal calibration plan)

April 2012 till April 2014:

Senior Quality Assurance Engineer at Franke Kitchen systems in Egypt Multinational company

Specific duties

  1. Develop, implement, communicate, follow up and maintain the Quality Health ,Safety and Environmental objectives
  2. promoting safety achievement and performance improvement throughout the organization using statistical tools
  3. Ensuring the execution of corrective action and preventive action in QHSE
  4. Monitoring daily performance for QHSE by gathering relevant data and producing statistical reports.
  5. Conduct QHSE training in a daily bases according to training plan
  6. Setting up and maintaining controls and documentation procedures.
  7. Internal Auditor for ISO 9001, 14001and OHSAS 18001 ,
  8. prepare for time meeting understand the requirements of other departments
  9. solving problem and improve the systems
  10. Develop, implementand maintainAudit Check List in order to check on the various departments
  11. Prepare monthly report about the status of QHSEoverall department contain an assessment and the needs for improvement
  12. Prepare the budget for QHSE department every year
  13. Conduct risk assessment in daily basis for every place and implement an action plans for every issue
  14. Conduct Job Safety Analysis for every activity and reviewed in daily basis

November 2009 till April 2012:

Assistant Quality Assurance Manager at spice kingdomfor medical herbsand seeds industries

Specific duties

  1. Develop, implement, communicate and maintain a quality plan to bring the Company’s Quality Systems and Policies into compliance with quality system requirements
  2. promoting quality achievement and performance improvement throughout the organization using statistical tools & Lean six sigma
  3. ensuring the execution of corrective action and compliance with customers' specifications;
  4. Monitoring performance by gathering relevant data and producing statistical reports.
  5. persuading reluctant staff to change their way of working to incorporate quality methods
  6. ensuring tests and procedures are properly understood, carried out and evaluated and that product modifications are investigated if necessary
  7. identifying relevant quality-related training needs and delivering training
  8. Setting up and maintaining controls in documentation procedures.
  9. Internal Auditor for ISO 22000 ,HACCP , BRC,14001 and 18001
  10. prepare for time meeting understand the requirements of other departments

, solving problem and improve the systems

  1. Maintainand implement HYGIENE plans and food safety.

12. Develop, implement and maintain KPI's.

13. Identify pesticides certificatesaccording to the customers need's

14.Develop, implementand maintainAudit Check List in order to check on the various departments.

15. Review packaging materials and implement supplier audit.

16. Prepare weekly report about the status of the Q.A department, people and overall department contain an assessment and the needs for improvement

17. Check the reconciliation of the lots identify the rework and scrap time and goods from the lot setting the preventive actions.

April 2007 till November 2009:

Quality Assurance officer in Marcyrl for Pharmaceutical industries

Marcyrl manufacturing under license for (ALTANA, MERZ, MULTIAPEX, QUINE and EPIC MISR)

In the Quality Control and Quality Assurance lab .

Specific duties:

  1. Monitors deviations from GMP in production and warehouse and reports there deviations as monthly report & for calculation performance measurement.
  2. Work with production in setting SOP, Batch Record & production improvementand prepare IPC documents.
  3. Receiving complaint and work with production in investigation and prepare the final report.
  4. Monitors and inspect the rework batches.
  5. Review of manufacturing & packaging records, cleaning & environmental control records and reports his comments to Q.A. manager.
  6. Checks and monitor calibrations & implements calibration plan & performs calibration of equipment( e.g. balances)
  7. Checks the use of components against the bill of materials
  8. Takes samples of the raw materials and intermediates and finished products, for release testing , stability and retention , inspect and sampling of returned goods
  9. Observe there execution of corrective and preventive action, incident report and NCR effectively.
  10. Quality Auditor ISO 9001:2008
  11. Observes the effectiveness of control of procedures and in process checks performed by production staff
  12. Followupof utilities like water station and HVAC
  13. Checks overprinted details for correctness and readability

In process Control in:

  • Wet And Dry Granulation, Tablet Compression,Tablet Coating.
  • Capsule Filling.
  • Blistering Process.
  • SyrupSemi-Solid Dosage Preparation & Filling.
  • Suppository FillingPreparation.
  • Packaging Process and sampling
  • get rid of reject material
  • Dispensing unit
  • Labeling the Hold and Released Labels in hold and released unit.
  • Cleaning process and line clearance for(solid, semisolid, syrup and suppository ) all stages of manufacture
  • Internal Auditor for ISO 9001

Experience in Equipments:

  • Shimadzu U.V.
  • Hardness Tester.
  • Friability tester.
  • Tablet & Capsule Disintegration Tester.
  • Conduct-meter.
  • PH-meter.
  • Torque Tester.
  • suppository Disintegration Tester
  • Total Organic Carbon (TOC) analyzer

July 2006 till April 2007:

Quality Assurance officer in EVA Pharma

In the Quality Control and Quality Assurance lab.

  1. In routine Analysis.

In process Control in:

  1. Checking the quality of all Packaging Lines in EVA Pharma (Solid , Semi Solid , Liquid)
  2. Checking the Hold and Released Labels in hold and released unit.
  3. Checking the quality of Printing unit(Batch no, Mfg.D, Exp.D …etc)
  • Inspection the quality of Dispensing Unit and operation.
  • Sampling
  • documentation: Annual Files

August 2005 till November 2006

Chemist in Segma Lab Dr: Iman Kamel

  1. In routine Analysis.

Experience in using:

  • Photometer.
  • Incubator , sterilization Apparatus , Micro pipettes
  • Cultures

Computer:

Application / Win 9X, Xp / MS Word / MS Excel / MS Power Point / Mini Tab / MS Project / ERP system / MS
Outlook / Lotus notes &Sage
Status / Good / Very Good / Good / Good / Good / Very Good / Good / Very good / Very good
Languages
understood / spoken / read / Write / Language
Very good / Good / Very good / Very good / English

Skills

Active, ambitious, hard worker, Welling to travel abroad, dynamic Personality

And ability to learn.

Hobbies

Basketball, Reading, Music, Chess, Walking.

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