Experience

TAJADOUD®

• Syrian Arab Republic
• International Trade and Development
• 1 - 100 Employee

• Co-Founder / Project Manger

  • Mar 2020 - Present



ISO-CERT company

• Syrian Arab Republic
• Business Consulting and Services
• 1 - 100 Employee

• Consultant & Trainer

  • Jun 2017 - Feb 2020

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



Pharmacated international Consultancy & Services

• Damascus, Syria

• Project Manager

  • Mar 2017 - Feb 2020

  - Taking responsibilities to supply: # Turnkey Cleanroom for Dawak Pharma. # Turnkey Machinery for Dawak Pharma. # Full Documentation, Registration and Training for Dawak Pharma. # Machines for Shifa Pharma. # Machines for Dimas Pharmaceutical Industries. # Machines for Thameco Pharmaceutical Industries. - 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. Show less



Ultramedica Pharma

• Damascus, Syria

• Management System Supervisor at QA & Management System Department

  • Nov 2015 - Mar 2017

  - 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. - 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.



Asia Pharmaceutical Industries

• Pharmaceutical Manufacturing
• 1 - 100 Employee

• • Jul 2011 - Jul 2015

  - Coordinate, conduct, and facilitate the activities of the validation that will include qualification of equipment, systems for both new and legacy ones.- Develop and generates IQ/OQ/PQ documents for indirect impact facility and building support systems (HVAC, water systems… etc) &manufacturing equipment.- Coordinate the implementation of process and cleaning validation activities and create final conclusions.- Prepare and develop all protocols needed for manufacturing process and cleaning validation.- Develop and/or review validation policies and projects master plans.- Review and develop SOP’s, protocols and programs in assistant of validation officers.- Interact and coordinate activities with support groups (Engineering, calibration… etc).- Prepare summaries of validation testing for regulatory submissions and present validations to regulatory agencies.- Review document and equipment changes requests related to validated system.- Assist in conducting audits focusing on validation programs and protocols.- Set plans for following up the monitoring of validated systems and revalidation activities.- Develop and coordinate environmental and water monitoring programs execution.- Set and agree validation time-scales and then ensure they are held on.- Mentoring and coaching members of the validation team as is necessary.- Participate in validation presentations and training programs.- Coordinate and supervise the efforts & activities of outside contractors and vendors in the commissioning & validation activities, (like: Pharma Access, Fabtech, IMA, Brevetti Angela, Rommelag & Bosch).- Work related duties and responsibilities as requested by the position manager and aim to develop the company.- The Projects that had been supervised:• New Solid Dosage Form Plant.• BFS Plant includes:* LVP Section.* SVP Section.• 100 ml Vial Plant.• Insulin & Prefilled Syringe Plant.• New Laboratory building. Show less

• • Mar 2011 - Jun 2011

  - 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.



Farmex Company SRL in Romania (Part of ASIA Group)

• Bucharest, Romania

• On-Line QA - Registration Coordinator at QA Department

  • Oct 2014 - Jun 2015

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



Alma Pharma in Homs (Part of ASIA Group)

• Homs, Syria

• Project Supervisor

  • Jul 2014 - Sep 2014

  - Coordinate, conduct, and facilitate the activities of the qualifying & repairing or modifying of equipments & systems. - Complying with cGMP for all parts of the company. - preparing for MOH audit. - Coordinate, conduct, and facilitate the activities of the qualifying & repairing or modifying of equipments & systems. - Complying with cGMP for all parts of the company. - preparing for MOH audit.



International Pharma in Russia (Part of ASIA Group)

• Nalchik, Russia

• On-Line QA - Validation Coordinator at QA Department

  • Nov 2013 - Mar 2014

  - Coordinate, conduct, and facilitate the activities of the validation that will include qualification of equipment, systems for both new and legacy equipment. - Develop, generate & review IQ/OQ/PQ documents for indirect impact facility and building support systems (HVAC, water systems… etc). Page 7 of 11 - Develop, generate & review IQ/OQ/PQ for direct impact manufacturing equipment. - Coordinate the implementation validation activities and create final conclusions. - Prepare, develop & review all protocols needed for manufacturing process and cleaning validation. - Develop and/or review validation policies and projects master plans. - Review and develop SOP’s, protocols and programs in assistant of validation officers. Show less



National Company for Pharmaceutical Industry (NCPI)

• Aleppo, Syria

• Physical and Chemical Laboratory Analyst at R&D Department

  • Aug 2009 - Feb 2011

  - Calibration Supervisor for lab Instruments. - Warehouse Responsible for raw materials and standards warehouse. - Internal Auditor with the company`s internal auditing Team. - Dealing with NaraTech & Escorting Them With their Developmental Visit. Page 4 of 11 - Analyzing drug products for Stability for multi dosage form and following up them during the stability study including make a protocol for stability study, entering and emitting samples from chambers and preparing certificates of analysis for stability study. - Analyzing drug products for Development section for multi dosage form. - Comparing the competitor (company product) and the original product (brand) "Comparative Test". - Analyzing rely 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). Show less



Natuline Cosmetics

• Aleppo, Syria

• Marketing and Sales Supervisor

  • Jul 2007 - Dec 2008

  - 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. - 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.