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Salah Elden Emad Ali

Quality Control Supervisor at Hikma Pharmaceuticals

Nasr City, Cairo, Egypt

Work Experience

  • Quality Control SupervisorFull Time

    Hikma Pharmaceuticals

    Oct 2022 - Present -2 yrs, 8 months

    Egypt , Cairo

    • Job Details:1- Responsible for training and following up new junior quality analysts in the probation period. 2- Assist in ISO requirements preparation to ensure documents completion, Monitor ISO system application in all branches to maintain company standards, prepare audits checklists to ensure the efficiency of ISO implementation and working as an internal auditor. 3- Prepare and setting SOPs of newly installed instruments such as GC and Polarimeter and training new employee on it. 4- Ensure implementation of CAPAs and risk assessments related to QC department. 5- Reviewing COA, OOS, and NCR of junior analysts and reporting it to the section-head to confirm it. 6- Responsible for a project of setting complete Specifications and test methods for all raw materials over (250 different raw material) according to the latest (BP, USP, JP, Handbook of Pharmaceutical Excipients, In-House). 7- Setting specifications for packaging materials, reviewing and following up its ordinary analysis. 8- Control chemicals and reagents (in and out) and setting excel sheets to calculate the balance of stock and rate of consumption and contact with suppliers to supply chemicals to the plant. 9- Coordinating with the planning department for arrangement priorities of the raw materials within the production plan. 10- Responsible for the Quality section head tasks in his absence.
  • Quality control supervisorFull Time

    EGPI

    Mar 2014 - Sep 2022 -8 yrs, 6 months

    Egypt , Cairo

    • Quality Control AnalystFull Time

      EGPI (Egyptian Group for Pharmaceuticals Industries)

      Mar 2014 - Feb 2017 -2 yrs, 11 months

      Egypt , Cairo

      • Job Details:1- Routine analysis of raw materials available on time & with high accuracy. 2- Working on HPLC, UV, IR and other instruments according to official references (BP and USP). 3- Routine Analysis of Water Samples. 4- Handling of the reagents & volumetric solutions. 5- Routine analysis of In-Process Control tests for Solid, Syrup Production Lines. 6- Daily calibration and monitoring of lab instruments. 7- Training and supervising the Investigation of the OOS (Out of Specifications) results and reporting directly to the section head in case of non-conforming results to take the required measures. 8- Documentation of the performed tests, calculations, results, issuing certificates and keeping the lab. documents stored and indexed.
    • Over the counter PharmacistFull Time

      Military hospital

      Aug 2012 - Sep 2013 -1 yr, 1 month

      Egypt , Cairo

      • Education

        • Technical Diploma in TQM

          American University in Cairo (AUC)

          Jan 2014 - Jan 2015 - 1 Year

        • Bsc. in Pharmaceuticals Sciences

          Cairo University (CU)

          Jan 2007 - Jan 2011 - 4 yr

        • High School - Thanaweya Amma

          Alsayeda Aisha Language school

          Jan 2006 

        Achievements

        - Setting specifications for packaging materials, reviewing and following up its ordinary analysis. - Control chemicals and reagents (in and out) and setting excel sheets to calculate the balance of stock and rate of consumption and contact with suppliers to supply chemicals to the plant. - Coordinating with the planning department for arrangement priorities of the raw materials within the production plan. - Responsible for the Quality section head tasks in his absence.

        Skills

        • Research
        • Microsoft Office
        • Pharmacopoeia
        • Sales and Marketing

        Languages

        • English

          Fluent

        Training & Certifications

        • ISO 9001:2015

          EGPI·2017
        • GMP

          EGPI·2016
        • LSSYB

          AUC·2015
        • TQM

          AUC·2015
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