Experience

Pharmaceutical Marketing

• United Kingdom
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• • Jan 2023 - Present

  • Supervise FPP and Stability section• Queries of Regulatory Department• Lead role on NME.• SOP, STM, Protocol, Reports. • Comparative Dissolution Profile.

• • Jun 2022 - Dec 2022



Indus Pharma (Pvt.) Ltd.

• Pakistan
• Pharmaceutical Manufacturing
• 300 - 400 Employee

• Assistant Manager

  • Mar 2017 - May 2022

  • Lead role in ISO 17025:2017 project • Documentation related to ISO 17025:2017 • Internal Audit • Method Validation/ Verification • Instrument Performance Qualification • Quality Control Risk Assessment. • Department Training Coordinator. • Lead role in ISO 17025:2017 project • Documentation related to ISO 17025:2017 • Internal Audit • Method Validation/ Verification • Instrument Performance Qualification • Quality Control Risk Assessment. • Department Training Coordinator.



Macter International Limited

• Pakistan
• Pharmaceutical Manufacturing
• 700 & Above Employee

• QC Executive

  • May 2016 - Mar 2017

  • Analysis of Finished Products and Stability. • To perform physical and chemical analysis of Inhaler. • Method validation. • To Check the Performance of new HPLC Columns. • To post all analytical results on SAP and to update the changes in specification on SAP. • Analysis of Finished Products and Stability. • To perform physical and chemical analysis of Inhaler. • Method validation. • To Check the Performance of new HPLC Columns. • To post all analytical results on SAP and to update the changes in specification on SAP.



Bosch Pharmaceuticals (Pvt) Ltd.

• Pakistan
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Quality Control Analyst

  • Mar 2014 - May 2016

  • Analysis of Semi-Finished products & Finished Products. • Analysis of water. • Regeneration of old HPLC Columns. • Analysis of Semi-Finished products & Finished Products. • Analysis of water. • Regeneration of old HPLC Columns.



Alina Combine Pharmaceuticals Pvt. Ltd.

• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Chemist

  • Mar 2011 - Feb 2014

  Analysis of Raw Materials. *Analysis of Semi-Finished products & Finished Products. *Analysis of water testing. *Line clearance *In-process inspection *Handling of Physical Instruments. *Maintain all Q.C Documentation Records. Analysis of Raw Materials. *Analysis of Semi-Finished products & Finished Products. *Analysis of water testing. *Line clearance *In-process inspection *Handling of Physical Instruments. *Maintain all Q.C Documentation Records.



Lexicon Pharmaceuticals, Inc.

• Pharmaceutical Manufacturing
• 200 - 300 Employee

• As a Trainee in Quality Control Department

  • Nov 2010 - Jan 2011

  Analysis of Raw Materials whether they fulfill USP/B.P specification & Packaging Material. Analysis of Finished Products. Maintain all the Q.C Documentation Records. Analysis of Raw Materials whether they fulfill USP/B.P specification & Packaging Material. Analysis of Finished Products. Maintain all the Q.C Documentation Records.