Karim Atef Email & Phone Number | * Vendor Qualification & Evaluation and follow it up. * Executive communications skills with all concerned departments related to VQ. * Submission of API-New sources to FDA. * Experienced Quality Control with a demonstrated history of working in the pharmaceuticals industry. * Skilled in Manufacturing, Quality System, GxP, Pharmaceutical Industry, and Standard Operating Procedure (SOP). * Knowledge and understanding of OOS, Risk assessment management and CAPA. In addition, carry out the required report for each of them. * To ensure compliance with established procedures relevant to the EHS management system in line with the organization. * Knowledge and understanding of analytical methodologies and instrumentation and Possession of good communication, trouble-shooting and function skills * Separation & analysis of RM & FP using GC (Agilent, Thermo), HPLC (Shimadzu, Agilent and Waters) in addition to Dissolution tester and Potentiometer and determine the assay for each one, Furthermore using (U.V. and FTIR Absorption), Karl Fischer, Disintegration, PSD by (Sieving, Malvern and Microscope) , Polarimeter, Penetrometer, T.L.C, Kjeldahl and pH meter.

Karim Atef

* Vendor Qualification & Evaluation and follow it up. * Executive communications skills with all con...
Riyadh, Riyadh, Saudi Arabia

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Karim Atef’s Phone Numbers +966 11 402 ****

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Karim Atef’s Location Riyadh, Riyadh, Saudi Arabia

Karim Atef’s Current Industry Riyadh Pharma

Karim Atef’s Prior Industry

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Vendor Relations Specialist

2021-01-01 00:00:00 - Present

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Karim Atef is a * Vendor Qualification & Evaluation and follow it up. * Executive communications skills with all concerned departments related to VQ. * Submission of API-New sources to FDA. * Experienced Quality Control with a demonstrated history of working in the pharmaceuticals industry. * Skilled in Manufacturing, Quality System, GxP, Pharmaceutical Industry, and Standard Operating Procedure (SOP). * Knowledge and understanding of OOS, Risk assessment management and CAPA. In addition, carry out the required report for each of them. * To ensure compliance with established procedures relevant to the EHS management system in line with the organization. * Knowledge and understanding of analytical methodologies and instrumentation and Possession of good communication, trouble-shooting and function skills * Separation & analysis of RM & FP using GC (Agilent, Thermo), HPLC (Shimadzu, Agilent and Waters) in addition to Dissolution tester and Potentiometer and determine the assay for each one, Furthermore using (U.V. and FTIR Absorption), Karl Fischer, Disintegration, PSD by (Sieving, Malvern and Microscope) , Polarimeter, Penetrometer, T.L.C, Kjeldahl and pH meter.