Summary
Overview
Work History
Education
Skills
Availability
References
Languages
Timeline
Generic

NAIMUL ISLAM

Maribyrnong,VIC

Summary

Aspiring as an overseas Industrial Pharmacist with 3.8 years’ experience in Analytical Research & Development having consistently strong academic results and ambition to secure a position at Pharmaceutical Industry. Primed to apply theoretical knowledge gained at university and skills acquired through work experience in a practical environment while learning from experienced professionals.

Overview

4
4
years of professional experience

Work History

Senior Officer (Analytical Research & Development)

Renata PLC, Bangladesh
03.2021 - 05.2024
  • Duration: 3.3 Years
  • Develop and optimize analytical methods for new pharmaceutical products or processes to meet specific quality and regulatory requirements
  • Analytical Method Development & Validation (Dissolution, Assay, Related Substances, Cleaning Method of Finished Product)
  • Development batch optimization analysis (Dissolution Profile, Multimedia Dissolution, Alcohol Dose Dumping Dissolution, Fesif/Fasif Media Dissolution)
  • Perform various quality control tests on raw materials for vendor approval
  • Working Standard Qualification & Preparation
  • Assessing and approving proposed changes to manufacturing processes, excipients
  • F Finished Product
  • Daily and schedule Calibration of laboratory instruments and equipment
  • (Weighing Balance, pH Meter, HPLC, IR, Centrifuge Machine, Hot Water Bath, Karl Fisher Tritrator)
  • Preparation of SOP, COA, Product Specification, Stability Study Protocol
  • Collect, record, and organize experimental data using laboratory equipment, software, and instrumentation
  • Monitor the stability of pharmaceutical products under different environmental conditions to determine shelf life, storage recommendations, specification

Officer (Analytical Research & Development)

General Pharmaceuticals Ltd., Bangladesh
10.2020 - 02.2021
  • Duration: 5 Months
  • Long Term and Accelerated Stability Batch Analysis By HPLC, UV, Karl Fisher Tritrator
  • OS, LIR report preparation, LIR investigation and solution
  • Managing the CAPA process by identifying, investigating, and resolving deviations, non- conformances, and other quality issues
  • Managing and controlling all relevant documents, including standard operating procedures (SOPs), batch records, and other quality records

Education

Bachelor of Pharmacy -

North South University
01.2018

Masters of Biotechnology Management -

La Trobe University, Melbourne

Masters of Pharmacology and Clinical Pharmacy -

North South University
01.2023

Skills

  • HPLC (Waters, Shimadzu, Agilent, Dionex)
  • FTIR (Shimazdu)
  • Dissolution apparatus
  • Karl Fisher(Metrohm)
  • RI
  • Melting point apparatus
  • UV-Spectrophotometer
  • PH meter
  • Centrifuge machine
  • Vacuum Oven
  • Shaking hot waterbath
  • Software: Empower3, Lab solution, Open lab, Chromeleon
  • Microsoft Office
  • Microsoft excel & PowerPoint
  • Team Management
  • Training in SOP
  • Problem solving related to HPLC and other instruments

Availability

I am holding an Austrian Student (Subclass 500) visa with Part-time/Casual work rights.

References

Dr. Abhiram Das, Deputy General Manager, ARD, SPD Renata PLC, Bangladesh, abhiram.das@renata-ltd.com, linkedin.com/in/abhiram-dash-ph-d-1a961034

Languages

English
Professional Working

Timeline

Senior Officer (Analytical Research & Development)

Renata PLC, Bangladesh
03.2021 - 05.2024

Officer (Analytical Research & Development)

General Pharmaceuticals Ltd., Bangladesh
10.2020 - 02.2021

Bachelor of Pharmacy -

North South University

Masters of Biotechnology Management -

La Trobe University, Melbourne

Masters of Pharmacology and Clinical Pharmacy -

North South University

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