Md. Nazmul Hasan

Experience

• 

  Active Fine Chemicals Limited

  Oct 2014 - Mar 2017

  Officer, Quality Control

  • Checking, analyzing & documenting all sorts of incoming sample and supplies of raw materials, intermediates and finished products of commercial, process validation, process optimization and product development batches.• Preparing and standardizing test and volumetric solutions.• Preparation of working standard and management of chemical reference standards.• Performing and documenting daily function check of QC Equipment.• Sampling of incoming raw & packaging materials.

• 

  Navana Pharmaceuticals Limited

  Mar 2017 - Sept 2021

  Executive, Product Development

  • New analytical method development, validation of raw material and finished product and reporting • New product Specification, TP, TR preparation. • Method transfer protocol preparation and execution.• Preparation of Dossier & other relevant documents.• Performing & documenting accelerated stability test & real time stability test of new & existing product.• STP, STR, SRS preparation. • Preparation of Drug Master File (DMF) of Active Pharmaceutical Ingredients (API). • Ensuring that safety equipment/dresses are worn in accordance with GLP.• Performing cleaning validation.• Establishing expiry dates and shelf life specification on the basis of stability test related to storage condition.• Reporting & investigating deviation, abnormal results, Out of Trend (OOT), and incident in QC laboratory.• Support to maintenance and troubleshooting of stability chamber. Show less

• 

  Renata Limited

  Oct 2021 - now

  • Preparation of Dossier & other relevant documents.• Excel sheet validation’s protocol and report preparation. • Ensuring that safety equipment/dresses are worn in accordance with GLP.• Project wise audit trail (HPLC, GC, UV, Potentiometer, etc.) review and reporting.• Development, validation and reporting of Cleaning validation’s analytical method. • OEL study.• Audit trail review and Data locking.• Performing risk assessment.• Deviation, CCR, CAPA, Incident, Out of specification (OOS) and Out of Trend (OOT) status sharing with departmental head/ In-Charge.• Troubleshooting of equipment. Show less • Reporting & investigating deviation, abnormal results, Out of Trend (OOT), and incident. • Method transfer protocol preparation and execution.• Performing & documenting accelerated stability test & real time stability test of new & existing product.• Receiving, Analysis and Reporting of cleaning validation samples.• STP, STR, SRS preparation. • New instrument method development. • Analysis and reporting of comparative dissolution profile.• Establishing expiry dates and shelf life specification on the basis of stability test related to storage condition.• Development, analysis and documentation of solubility profile, decontamination study.• Stability sample reconciliation.• Support to maintenance and troubleshooting of stability chamber. • New employees training need preparation and training coordination. Show less

  • Assistant Manager, Quality Control

    Jan 2023 - now

  • Senior officer. Quality Control

    Oct 2021 - Jan 2023