SABRI MOHAMMED SABRI ELHESSOUN, Total Quality Management Manager

SABRI MOHAMMED SABRI ELHESSOUN

Total Quality Management Manager

Saudi Bio-Acids Company

Lieu
Arabie Saoudite - Jeddah - Al Waziriyah
Éducation
Master, MBA - Organization Management
Expérience
31 années, 1 mois

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Expériences professionnelles

Total des années d'expérience :31 années, 1 mois

Total Quality Management Manager à Saudi Bio-Acids Company
  • Arabie Saoudite - Jeddah
  • Je travaille ici depuis avril 2018

Company Details: Under construction in Jeddah to producing Citric Acid and its salts, the first factory in Arab countries.

Responsibilities:
* • Preparing all necessary documents for ISO & GMP Certificates. Preparing Policies / BMR / Creation more than 100 SOP (s).
* Furnishing laboratories to be suitable for chemical, physical, and
microbial tests and preparing documents.
* To issue registration certificates process for Factory /products from
Authorization Regulations.
* Planning Controlling of HSE for Employees and Planning Program
to avoid any risk against the environment in keeping the workplace
safe.
* Management of R & D in their work by studying manufacturing
process miniature of raw materials and bacteria developed (Growth
& Harvesting) into Laboratory, a study of the stability of products,
and study validation of analysis & manufacturing.
I have a good experience through my working in Bio Acids
Manufacturing Company and my working in
Pharmaceutical Industry to creating documents and
monitor quality processes to ensure that equipment,
instruments, and people produce products and services
by company and industry regulatory requirements by
providing & developing the quality strategy, policies,
processes, standards, forms, objectives, and systems for
the Company.

Position: Assistant Manager at Regulatory Affairs Lasts three years. / Assistant QA Manager for two à Pharmaceutical Solutions Industry
  • Arabie Saoudite - Jeddah
  • mars 2001 à mars 2018

Department: QC / QA and finally to Regulatory Affairs Department.

Company Details: Lead in pharmaceutical industry in Middle East.

Responsibilities:
• Setting for Drug license variations and renewal registrations.
• Self-Inspection Leader. Follow the Guidelines of GMP.
• Supervised all documents related to Manufacturing Operations.
• Manufacturing Monitoring, monitoring all Filling Machines, monitoring all Packing Lines, and Controlling QC / QA samples.
• Training new staff.
• Chemist at In-process Chemistry Lab. For releasing batches (during Preparations, filling). Testing physical of manufacturing bottles & Calibration of some Instruments.

Salesman Supervisor à Saudi Plastic Cards
  • Arabie Saoudite - Jeddah
  • avril 1999 à mars 2001

Company Details: Lead in manufacturing of plastic cards in KSA.

Responsibilities:
* During this period, I got experience in quotation, collecting money,
and making contracts with most Hospitals, Polyclinics, and
Insurance companies in Jeddah / Tief.

Chemist à Pharmaceutical Solutions Industry
  • Arabie Saoudite - Jeddah
  • mars 1993 à avril 1999

Analyze & Releasing Batches / Raw Materials (during
preparations, filling, and passing to Quarantine Store) in changing
shifts.
* Physical testing of manufacturing bottles & Calibration of some
Instruments.

Éducation

Master, MBA - Organization Management
  • à Cambridge International Collage
  • août 2012

I made a questionnaire as graduation research, the subject o was ... Assessment Success of the administrative type of any organization and I got a very good mark.

Baccalauréat, Bachelor of Science – Biochemistry
  • à King Abdul Aziz University
  • février 1993

I edited the Vancomycin Effects as graduation research, and I got a very good mark.

Specialties & Skills

Document Control
Registration
Quality Inspection
ISO Auditor
Manufacturing & laboratories training
Negotiate Contracts & Quotations
Safety & Healthy Management
Control Documents
Building strong team and developing communications ways with them.
Developing and writing clear arguments and explanations for new product licenses and license renewal
Quality Operation & Product by reducing the cost & time
MATERIALS MANAGEMENT
CALIBRATION
FILE MANAGEMENT
CONTRACT MANAGEMENT
ISO Inspection Leader

Langues

Anglais
Expert

Formation et Diplômes

ISO CERTIFICATE (Certificat)
Date de la formation:
January 2007
PROJECT MANAGEMENT (Formation)
Institut de formation:
ALFALAH
Date de la formation:
July 2020
Durée:
35 heures

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