Yousef Mohamed

Experience

• 

  EGPI (Egyptian Group for Pharmaceutical Industries)

  Sept 2016 - Nov 2018

  QA Specialist

  In solid area-During process checks following things needs to be checked -following and checking problems during granulation and compression-checking appearance tablet during compression and coating -checks physical parameters and attributive features physical parameters as:Temperature ,Time,pressure,weight,hardness,disintegration time,particle size,loss on drying,viscosity,PHAttributive features:visible impurity,colour,integrity,fractional part-checking cleanliness of area ,equipment and line clearance -Checking the weights of in process materials-checking labelling status of quarantine materials-Ensure correct materials are brought for manufacturing correct--verification of status labels on area ,equipment and process containers In semi solid area -Ensure hygiene operators according to GMP-Insepection of different packing materials in production area as tubes ,bottles -follow up during prepration in production area according batch record and procdures -check weight of tubes during filling -Sampling of all IPC test and finished product sampling -Testing on tubes during process as weight ,leakage-ensure batch number on tubes In Syrup area:-follow up prepration according to batch-following prepration and filling -checks volumes of bottles and leakage during filiing -checking cleanliness of machines before filling and correct labelling during prepration and filling-following CIP after end processing -Sampling water for ensuring conductivity and PH results Centeral packaging -(Inspection of different packaging material (1ry and 2ry-Ensure batch number correct on boxes during packaging according to batch record -enure leaflet in boxes folding correctly- Sampling finished product for retained and stability according to plan-ensure warnings and price on boxes before packaging عرض أقل

• 

  Hikma Pharmaceuticals

  Nov 2018 - Nov 2020

  QA Officer

  • Ensure GMP Compliance for daily activities during batch manufacturing (cleaning, Line clearance, Deviation handling, calibration, Preventive maintenance)• Review each batch record & initiate investigation for observations found in batch records.• Review QA SOP’s prepared by QA and other related departments• Follow-up implementation of CAPAs resulted from failure investigations• Participate in preparing for receipt of external audits.• Perform daily rounds in production area and warehouses to ensure implementing GMP during daily activities.• Review and approve Manufacturing and Packaging formula, manufacturing and packaging Instructions• Review and approve artworks design proofs عرض أقل

• 

  Dulex Lab

  Nov 2020 - Oct 2022

  QA Supervisor

  • Arrange, perform and follow up self-inspection activities.• Receive and assess deviations and identify relevant corrective and preventive actions• Receive and assess change controls and identify implementation requirements, and follow up implementation • Perform failure investigations to identify root causes and necessary CAPAs• Follow-up implementation of CAPAs resulted from failure investigations• Manage complaints, perform investigations to identify root causes and CAPAs• Participate in implementation of corrective actions resulted from external audits• Participate in GMP training lectures• Perform daily rounds in production area and warehouses to ensure implementing GMP during daily activities.• Review and give final approval of batch records when delegated by QA manager. عرض أقل

• 

  Gypto Pharma

  Oct 2022 - May 2024

  Quality Operation

  Devaiton management systemOOS/OOT management systemCAPA management systemAuditing ProcessAPQRChange control management system