Mahmoud Samy

Mahmoud Samy

Pharmacist

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location of Mahmoud SamyEgypt

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  • Timeline

  • About me

    product QA Manager

  • Education

    • Sakr Koresh experimentaly language school

      1992 - 2005
      General secondary certificate
    • Cairo University

      2005 - 2011
      Bachelor's degree Pharmaceutical Sciences

      Activities and Societies: Shabeb Misr family

  • Experience

    • Normandy pharmacy

      Sept 2011 - May 2012
      Pharmacist

      Selling drugs to patients.

    • EIMC Pharmaceuticals

      Jul 2012 - Aug 2014
      QA specialist

      • Record and document results and compare to expected results.• Monitoring the manufacturing process from A to Z.• Implementing and revising SOPs.• Creating compliance department inside QA department.• Making annual product review for all products.• Making data trending analysis and study their results.

    • Sanofi

      Sept 2014 - now

      • Managing Clearance & materials planning team.• Setting the MRP on Weekly basis based on Forecast changes & Sales momentum.• Follow with the clearance agent the clearance process for the imported materials till being received at the site.• Supervising the issuance & the updates for the annual importation plans at the EDA.• Responsible for the exportation process for some products.• Ensure local coordination on all Sanofi Group (internal) and third-party (external) sourcing issues.• Review local inventory levels to meet business requirements, ensuring effective forecasting systems are in place which guarantee reactivity to the market demands, in line with business forecasts turnovers and investment objectives.• Build a teamwork atmosphere to ensure proper flow of work in the department and its effectiveness.• Build together with the team members and HR development plans to further enhance the skills and competencies of the team, through coaching, delegation and training. Show less • Setting the production plan for all the production departments taking into consideration customer delivery requirements, production capacities, materials availability & maintenance schedules. • Follow-up with all departments (Production, Quality & warehouse) the implementation of the production plan, the release & setting priorities in order to have the required SKUs available for sales in the right time.• Setting MRP for packaging materials, APIs & Auxiliary materials for covering the production plan & the sales Forecast.• Maintain and analyse with the Market SC the DRP (Demand Requirement Planning) on Monthly Basis to be able in implementing the MPS (Master Production Schedule).• Implementation of MPS and discuss with all IA Parties (Production, QC, QA,…) the possibility of achieving it • Liaise with the production manager & each production Section Head to establish the production and delivery program of the Month on daily level• Divide the Monthly MPS to Weekly Production & Delivery Plan according the Production Capacities.• Creating all the Process orders concerning manufacturing & Packaging processes• Creating all the Purchase Orders (PO) for all the Toll-Out Manufacturing Products for All Sub-contractor• Controlling all the Production Deliveries & Schedules according to the Sales Accuracy in order not to affect our Inventory Level and Value.• Implement the Safety Stock Coverage Policy for all our Products to cope with the Service Level Agreement between Plant Logistics and Market SC• participate for achieving all the Plant Logistics KPI’s related to the FG Stock Coverage and Schedule Adherence and Customer Compliances with the Market SC• Follow up with the Quality Operations all the releases and set Priorities for the urgently Needed SKU's to be Ready and available for Sales.• Project Leader for Kinaxis Rapid Response Going live on Cairo Site => Done on May 2022. Show less - From march 2017 promoted to be senior QA shopfloor officer.- Responsible for organizing the tasks on the shopfloor team.- Performing annual product review for Sanofi products & organizing its annual plan with the shopfloor team.- Initiating process validation protocols for new & current products.- Leading investigations for all kinds of deviations, OOS & OOTs.- Performing quality tours in the production areas to ensure the implementation of the cGMP.- Dealing with the MOH inspectors for the finished goods & materials destruction issues.- Act as a qualified officer for the final release of the sterile & non-Sterile finished goods using SAP ATHENA.- Act as a qualified officer for the final release of the imported goods using SAP CEP system. Show less

      • Product QA Manager

        Apr 2024 - now
      • Section head for Logistics & Material planner

        Jul 2022 - Apr 2024
      • Senior Production Planner

        Apr 2020 - Jul 2022
      • QA Senior QA shopfloor officer

        Mar 2017 - Mar 2020
      • QA Specialist

        Sept 2014 - Mar 2020
      • QA Officer

        Sept 2014 - Mar 2017
  • Licenses & Certifications

    • Bachelor degree in pharmaceutical science

    • General TQM

      AUC - School of Continuing Education