Ayham Mufti

Berufserfahrung von Ayham Mufti

• Bis heute 2 Jahre und 9 Monate, seit Jan. 2022

  Project Manager

  MSKI Pharma

• Bis heute 4 Jahre und 10 Monate, seit Dez. 2019

  Cofounder / Purchasing & Project Manager

  TAJADOUD Drug Store & Pharmaceutical Business Company

  -Purchasing the RM from the suitable and approved source for the local market. -Managing the machines and new pharmaceutical projects orders.

• 2 Jahre und 7 Monate, Juni 2017 - Dez. 2019

  Consultant and Trainer in The Pharmaceutical Projects Department

  ISO Cert Company

  -As consultant for Pharmaceutical Audits. -As Trainer for Pharmaceutical GMP & Validation Courses.

• 2 Jahre und 9 Monate, Apr. 2017 - Dez. 2019

  Project Manager in The Pharmaceutical Projects Department

  Pharmacated International Consultancy & Services

  -Taking responsibilities to supply: #Turnkey project for Dawak Pharma Project. #Machines for: Shifa, Dimas, Thameco. #Requalification for AWK. #Qualification for Zein Pharma. #Qualification for ML Drug Store. -Working on new clients: #Syringe Manufacturing Plant. #Cosmetic Manufacturing Plant. #Kidney Dialysis Fluid Solution Manufacturing Plant. #Shampoo Manufacturing Plant. #New Sterile Pharmaceutical Company in GCC. #New 4 Turnkey Projects in Syria. -As an agent for Austar & Tofflon in Syrian Market.

• 1 Jahr und 5 Monate, Nov. 2015 - März 2017

  Management System Supervisor in QA & Management System Department

  UltraMideca Pharmaceutical Industry

  -Complying with ISO Management Systems for all parts of the company. -Preparing for ISO audit. -Complying with cGMP for all parts of the company. -Preparing for MOH audit. -Issuing & developing BMRs. -Training Supervisor. -Health & Safety Supervisor.

• 4 Jahre und 1 Monat, Juli 2011 - Juli 2015

  QA - Validation Coordinator in QA Department

  ASIA Pharmaceutical Industry

  -Coordinate, conduct, and facilitate the activities of the validation that will include qualification of equipment, systems for both new and legacy equipment. -Develop and generates IQ/OQ/PQ documents for direct/indirect impact machines and utility systems. -Coordinate the implementation of process and cleaning validation activities. -Prepare and develop all protocols needed for manufacturing process and cleaning validation. -Develop and/or review validation policies, plans, SOP’s, protocols and programs.

• 9 Monate, Okt. 2014 - Juni 2015

  On-Line QA - Registration Coordinator in QA Department

  Farmex Company SRL in Romania (Part of ASIA Group)

  -Coordinate and conduct the Master Batch Manufacturing Record to comply with WHO and Romanian Requirements.

• 3 Monate, Juli 2014 - Sep. 2014

  Project Supervisor

  Alma Pharma (Part of ASIA Group)

  -Coordinate, conduct, and facilitate the activities of the qualifying & repairing or modifying of equipment’s & systems. -Complying with cGMP for all parts of the company. -Preparing for ISO & MOH audit.

• 5 Monate, Nov. 2013 - März 2014

  On-Line QA - Validation Coordinator in QA Department

  International Pharma in Russia (Part of ASIA Group)

  -Coordinate, conduct, and facilitate the activities of the validation that will include qualification of equipment, systems for both new and legacy equipment. -Develop and generates IQ/OQ/PQ documents for direct/indirect impact machines and utility systems. -Coordinate the implementation validation activities. -Prepare, develop & review all protocols needed for manufacturing process and cleaning validation. -Develop and/or review validation policies, plans, SOP’s, protocols and programs.

• 4 Monate, März 2011 - Juni 2011

  Analytical Supervisor in R&D Department

  ASIA Pharmaceutical Industry

  - Calibration supervisor for lab Instruments. - Preparing the Product Master File for some products. - Preparing the Product Development File for some products. - Preparing the analytical method validation for the product. - Establishing the Cleaning Validation in the company.

• 1 Jahr und 7 Monate, Aug. 2009 - Feb. 2011

  Analyst in the Physical and Chemical Laboratory in R&D Department

  National Company for Pharmaceutical Industry (NCPI)

  -Calibration Supervisor for lab Instruments. - R&D Warehouse Responsible. -Internal Auditor. -Analyzing drug products for Stability. -Analyzing drug products for Development section. -Comparing the competitor (company product) and the original product (brand) "Comparative Test". -Analyzing samples for suppliers to build vender list. -Analyzing Raw Materials and R&D finish product for R&D release. -Making the analytical method validation for the product. -Preparing standard operation procedure (SOPs).

• 1 Jahr und 6 Monate, Juli 2007 - Dez. 2008

  Marketing and Sales Supervisor

  Natuline (French Cosmetic Brand) Aleppo Branch

  -A marketing team player, organizing long-term tactics for the team. -Dealing with a large range of customers. Solving marketing & sales issues and making decisive decisions.