Ahmed Alaa El-Din

Product Development Manager at Danone

• Egypt - Cairo
• My current job since January 2018

Product Development Technologist at Danone

• Egypt - Cairo
• October 2016 to December 2017

Operational QA Officer at GlaxoSmithKline

• Egypt - Cairo
• May 2016 to September 2016

Technical Services Lab Analyst at GlaxoSmithKline

• Egypt - Cairo
• March 2014 to April 2016

 Management of Calibration routines in the Analytical laboratories.
 Analytical Method Transfer of Products introduced into or out GlaxoSmithKline El-Salam Site
 Analytical Method Validation of Newly Developed Method & its Periodic Review.
 Analytical Method Development for New Products introduced to the Site.
 In-vitro bioequivalence testing according to Periodic and regulatory Routines.
 Managing Chemical Stores.
 Cleaning Validation
 Issuing Technical Documentations on various Analytical techniques, Equipment Calibration and operation routines.

Quality control analyst at Glaxosmithkline

• Egypt - Cairo
• September 2013 to March 2014

 Analysis of GlaxoSmithKline's Finished Products of Different Dosage forms (Capsules, Syrups, Tablets, Ampoules, Suspensions and Semisolids) according to Weekly Plan.
 Analysis of 3rd Party Products "Novartis & Sandoz"
 Analysis of Stability Samples along with the Release Samples.
 Analysis of Some Purchased Raw Materials and APIs According to GlaxoSmithKline’s Specifications
 Working on UPLC & HPLC (Waters & Agilent), GC (Agilent), Atomic and UV Spectroscopy instruments (Agilent).
 Performing Method, Process & Cleaning Validation
 Responsible of Chemical Reagents Inventory and its Management
 Member of The Process Validation Project “Validation of all GlaxoSmithKline’s Current Products on all Production’s machinery”

Quality Control Analyst at Eva Pharma

• Egypt - Cairo
• October 2012 to September 2013

Analysis of Eva Pharma's Finished Products of Different Dosage forms (Capsules, Syrups, Tablets, Ampoules, Powders & Semisolids) according to Daily Plan.
 Analysis of 3rd Party Products "Pfizer"
 Scale up Analysis of R&D's New Products.
 Analysis of Some Purchased Raw Materials and APIs.
 Working on UPLC & HPLC (Agilant & Merck LaChrome), GC (Agilant & Varian), Atomic and UV Spectroscopy instruments.
 Troubleshooting and resolving operations issues.
 Internal Calibration of instruments according to work instructions to ensure compliance to standards. (Responsible of The Daily Calibration of the pH meter)
 Preformed Method Validation for both the assay and Dissolution methods of finished Products to ensure products’ compliance to standards. (Deslorat Tab., Prazolam Tab.)
 Preformed Process Validation (CTD) of Finished Products (Thiotacid 600mg tab.)
 Introduced the Labelling system to the Whole quality Department throughout all the Labs