Mostafa Refaee

Quality Control Section Head at Interpharm
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Contact Information
us****@****om
(386) 825-5501
Location
Cairo, Cairo, Egypt, EG

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5.0

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Eman Ateia

I worked with Dr. Mostafa for short time, but during this period, He was keen on his job and didn't hesitate to help anyone. Very patient when it comes with investigation. Scientifically strong and has very good knowledge of analytical pharmaceutical skills. I would recommend him to any company looking for a team leader with strong technical background.

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Experience

    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Quality Control Section Head
      • Nov 2019 - Present

    • Saudi Arabia
    • Pharmaceutical Manufacturing
    • 400 - 500 Employee
    • Methodology Senior Analyst
      • Dec 2018 - Oct 2019

      Prepare test method of analysis for new products (R&D trials). Perform analytical test method validation, Protocol & report. Perform cleaning validation protocol. Perform Dissolution Profile for different types of products "Tablet, Capsules and Suspension" Perform accelerated stability studies for R&D trials. Troubleshoot and resolve operations issues. Conduct training to fresh analyst. Prepare SOP related to methodology department. Contribute with other departments ( QC , QA & RA ) Maintains laboratory supplies inventory required for Stability analysis. Responsible for handling the global changes affecting stability and methodology. Responsible for fulfilling all regulatory requirements related to stability and methodology. Participate in stability out-of-specification and failure investigations. Responsible for following up stability equipment calibration & maintenance and ensure appropriate documentation and archiving. Show less

    • Egypt
    • Pharmaceutical Manufacturing
    • 400 - 500 Employee
    • Methodology Analyst
      • Mar 2017 - Nov 2018

      • Preparing test methods for new products. • Validate the assay methods of finished products. • Performing Dissolution Profile for different types of products "Tablet, Capsules and Suspension" • Troubleshoot and resolve operations issues. • Review calibration and validation of all devices at the lab • Preparing test methods for new products. • Validate the assay methods of finished products. • Performing Dissolution Profile for different types of products "Tablet, Capsules and Suspension" • Troubleshoot and resolve operations issues. • Review calibration and validation of all devices at the lab

    • Egypt
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Quality Control Specialist
      • Nov 2013 - Feb 2017

      - Analysis all raw materials. - Preparing chemical reagents & indicators. - Prepare volumetric solutions. - Perform analytical test method validation, Protocol & report. - Perform stability intervals on finished products. - Handling with instruments like (HPLC, UV, Balance and PH meter). - Analysis all raw materials. - Preparing chemical reagents & indicators. - Prepare volumetric solutions. - Perform analytical test method validation, Protocol & report. - Perform stability intervals on finished products. - Handling with instruments like (HPLC, UV, Balance and PH meter).

Education

  • Ain Shams University
    Science

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