Experience

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  Hikma pharmaceuticals

  May 2008 - Feb 2014

  responsible for comparative dissolution studies and analytical methods validation and method development in cooperation with my team , Maintain reference standards system ( developing and inventory ) carry out internal auditing activities responsible for raw material suppliers qualification in cooperation with procurement department participate in cleaning validation , and equipment qualification activities Updated and created the QC SOPs in accordance to the local regulatories and international guidelines , Performed daily tour in the QC to assure compliance to the specifications,maintained Hikma pharma training system in the QC by delivering training and creating training plans for the on-job and new-hired training. Tested and evaluated pharmaceutical finished product and raw material samples according to Hikma pharma specifications, and licensor companies specifications like Eli Lilly, J&J and BAYER .Participated in analytical method development and method validation activities

  • QC Compliance and validation Supervisor

    Jan 2013 - Feb 2014

  • Quality Control Compliance senior

    Jan 2011 - Dec 2012

  • Quality Control analyst

    May 2008 - Dec 2010
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  Natural wellness industries sdn bhd

  Mar 2014 - Apr 2015

  Research project manager

  Project Leader for the company's mission to produce high value herbal products through a group of research projects thank includes standardization of herbal extracts, preclinical pharmacological and toxicological studies, and clinical trials (Phases I, Phase II and Phase III)My role included all the project management activities from scope setting till execution and controlling of activities and outputs.

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  Makin research center

  May 2015 - May 2017

  Executive technical manager

  Managing and controlling ongoing studies and research activities to insure compliance to the international guidelines and local authorities and meeting customers due dates

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  Inad pharmaceuticals

  Jun 2017 - Dec 2020

  Quality control & analytical research manager

  Managing the Quality Control department responsible for inspection and release of raw materials, packaging materials and finished products. Various processes are designed in compliance with GXP and regulatory and requirements. Assuring the implementation of carefully constructed SOPs for routine processes and for date integrity, deviation control, OOS and OOT handling, CAPA followup, and continuous improvement processes. Managing the analytical and assessment aspects of products development, from analytical method development using various techniques such as HPLC and GC, to final product evaluation using QC tests according to pharmacopoeias, and the conduction of evaluation studies which includes comparative in-vitro dissolution and stability as per international guidelines such as ICH and, EMA and FDA guidelines.Hiring and performance management of key personnel in both departments. Show less

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  Riva pharma

  Jan 2021 - Jun 2023

  Qc an analytical research manager
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  Hayyan scientific

  Jul 2023 - now

  Managing director

  Hayyan Scientific offers a wide spectrum of products and services to the pharmaceutical and scientific communities, from contract research to high quality products like reference standards and lab consumables and instruments