Experience

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  One Pharma Ltd.

  • Bogra District, Rajshahi, Bangladesh

  • Senior Executive Product Development

    • Oct 2020 - Present
    • Bogra District, Rajshahi, Bangladesh

    1. To perform Examine and analyze raw materials, lab batch & PV batch finished products according to written procedure/BP/USP & prepare analytical reports.2. To perform analytical method validation of the finished product and raw material.3. To prepare Working Standards by Standardizing with Analytical reference standards.4. To maintain GLP and housekeeping in the laboratory and to take corrective measures for any deviation.5. To initiate any other activities, reports related to QC/QA6. To write and review other quality documents7. Prepare Reagents and Standardization.8. To perform Method verification Analysis.9. To perform analytical method Validation.10. To perform cleaning validation analysis.11. Maintain proper requisition channel with headquarters on time.12. Decide on and order the resources that are required and ensure stock levels remain adequate.13. Execute factory manufacturing strategic plan and align it with general plant strategy.14. Organize the repair of any damaged equipment.15. Collaborate with other factory managers to find best practices and the best solution.

• 

  SUN PHARMA

  • Gazipur District, Dhaka, Bangladesh

  • Quality Control Officer

    • Dec 2017 - Sep 2020
    • Gazipur District, Dhaka, Bangladesh

    1. To perform all Quality Control Equipment Calibration like HPLC, UV Spectrophotometer, Dissolution FTIR, etc.2. To perform Examine and analyze raw materials, intermediates & finished products according to written procedure/BP/USP & prepare analytical reports.3. To perform analytical method validation of the finished product and raw material.4. To prepare Working Standards by Standardizing with Analytical reference standards.5. To maintain & check various reagents in the QC lab.6. To maintain GLP and housekeeping in the laboratory and to take corrective measures for any deviation.7. To initiate any other activities, reports related to QC/QA8. To write and review other quality documents9. Prepare Reagents and Standardization.10. To perform Method verification Analysis.11. To perform analytical method Validation.12. To perform cleaning validation analysis.

• 

  UniMed UniHealth Pharmaceuticals Ltd.

  • Gazipur

  • Quality control officer

    • Sep 2016 - Dec 2017
    • Gazipur

    1. Be responsible to perform routine work such as sampling & analyzing testing of RM, PM & Products according to the approved written procedures i.e. specific STPs.2. Be responsible to ensure that the reagents are properly prepared & labeled according to written instructions, maintained specific storage conditions, standardized & revalidated if necessary, discarded after the shelf life, and maintained necessary records.3. Be responsible for operating the Equipment of HPLC, UV, FTIR, etc., and regular and proper maintenance of the analytical labs and analytical equipment/instruments. 4. Be responsible for daily performance checks of balances & pH meter and calibration of all measuring equipment/ instruments at fixed intervals according to the Calibration Program.5. Be responsible to ensure that all generated data (accurate, clear & truthful) must be fully documented and recorded in specific formats, log books & registers.6. Be responsible to ensure that the cGMP, GLP (Good Laboratory Practice), Environment, Health & Safety (EHS) guidelines.