Ayham Mufti

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

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

-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.

-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.

-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.

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

-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.

-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.

- 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.

-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).

-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.