Md Abu Taleb

Experience

• 

  Kohinoor Chemical Company (BD) Ltd.

  Dec 2007 - Feb 2009

  Production & Quality Control Officer

  OutlineSupervised and controlled effectively all manpower for the production in manufacturing floors.Key Responsibilities• Ensured operation of designated machines to its maximum permitted level and helped to organize manpower accordingly. Paid attention the capacity to run the production operation smoothly for achieving employer target.• Established priorities and revised overall schedules where necessary to ensure efficiency.• Confirmed all equipment is maintained and run properly.• Tested of raw materials, IPC products and monitored of IPC products during production of soap and cosmetics in the production floor.• Worked for the development of soap & cosmetics in lab process.• Tested samples for numerous chemical analysis. Show less

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  The ACME Laboratories Ltd.

  Mar 2009 - Aug 2009

  Quality Control Officer

  OutlinePerformed analytical activities of IPC products for solid dosages form and raw materials according to SOP.Key Responsibilities• Performed analytical chemistry based assays on new and existing methodologies.• Sampled, inspected and evaluated of incoming raw materials and bulk products. • Tested physical and chemical characteristics of new active pharmaceutical ingredients. • Carried out analytical activities of IPC products according to GLP.• Worked in a cGMP laboratory with strong emphasis on data handling.• Identified risks and key control activities. Show less

• 

  Popular Pharmaceuticals Limited

  Aug 2009 - now

  OutlineI am leading stability study branch in Quality Control Department.Key Responsibilities• To ensure stability study of finished products, supervising, organizing and monitoring of analysis and assuring the completeness of all activities accurately. • To prepare stability study protocol, program, yearly plan, monthly schedule, data sheet (TRS/ARS) and report for international and domestic market on time.• To confirm proper storing and removing of all stability study samples inside the stability room/chamber for mentioned storage condition and timely monitoring.• To check and review all types of stability study/QC analytical data, documents, reports and log books for test solution, volumetric solution and analytical log books.• To evaluate the stability and shelf life of products by assessing analytical test reports of analyst.• To maintain proper communication, co-ordination, co-operation and liaison with all other relevant departments for smooth operation. • To monitor strictly the regulatory compliance and perform any other QC related assignment as per requirement of the department head.Note: I have developed many analytical method as research work, however could not publish in any journal since it highly prohibited to disclose to public because company is the owner of the developed method. Show less • Preparing and maintaining of stability study report according to internal and external auditor’s standards and communicate with international marketing department. • Checking and reviewing all types of stability study/QC analytical data, documents, reports and log books for test solution (TS), volumetric solution (VS) and analytical log books.• Analytical method development of products, preservatives and related substances.• Performing validation and cleaning validation as well as establish their recovery study.• Conduct analytical activities and troubleshooting of analytical instruments in accordance with others requirement.• Performing calibration of analytical instrument as per requirement of superior.• Monitoring the preparation and standardization of volumetric solution and test solutions.• Performing re-analysis of intermediates, final and stability study products while existing analyst found unsatisfactory result and handling of laboratory incidents and deviation for the evaluation of product quality. Show less • Performed analytical chemistry assays based on new and existing methodologies.• Analysis of various pharmaceutical products including solid and liquid doges form (e.g. Tablet, Capsule, , Oral saline, FPS, PFI , Insulin, Amino Acid, Ophthalmic, Inject-able, Infusion & Dialysis fluids). Performed analytical chemistry assays based on new and existing methodologies.• Sampled, inspected and evaluated of incoming raw materials and bulk products. • Tested physical and chemical characteristics of new active pharmaceutical ingredients. • Performed analytical activities of IPC products according to GLP.• Recorded and archived of documents & reference samples of IPC products.• Worked in a cGMP laboratory with strong emphasis on data handling.• Analysis of process validation sample and documentation timely.• Identified risks and key control activities. Show less

  • Assistant Manager Quality Control

    Jan 2021 - now

  • Senior Executive-Quality Cotrol

    Jan 2014 - Dec 2020

  • Executive-Quality Control

    Jan 2013 - Dec 2013

  • Quality Control Officer

    Aug 2009 - Dec 2012
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  East Texas A&M University

  Aug 2024 - now

  • Graduate Research And Teaching Assistant

    Aug 2024 - now

  • Graduate Teaching Assistant

    Aug 2024 - now