Summary
Overview
Work history
Education
Skills
References
Timeline
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Mohammad Tanvir Hasan

Mohammad Tanvir Hasan

London,London

Summary

Accomplished Industrial Pharmacist with 5 years of experience in pharmaceutical manufacturing, quality control, and regulatory compliance. Expertise in manufacturing processes. Adept at performing physical and chemical tests of in-process materials and finished products, following GLP. Skilled in leading production teams, optimizing workflows to reduce downtime and increase yield. Proficient in preparing regulatory documents (SOPs, BMRs, BPRs) in line with GDP guidelines, and working with validated systems like QMS, LIMS, and BME. Experience in equipment qualification and maintaining audit-readiness for FDA, GMP, and other regulatory inspections. Strong commitment to safety protocols, particularly in handling hazardous materials, and consistently ensuring compliance across operations.

Overview

5
5
years of professional experience

Work history

Senior Production Pharmacist

Eskayef Pharmaceuticals Ltd.
Gazipur
2020.06 - 2024.08
  • Ensures precision in formulation, dosing, and manufacturing processes, minimizing errors in production.
  • Manufacturing of products following FDA, GMP, and other regulatory guidelines to ensure the production of safe, compliant pharmaceutical products.
  • Leading production teams, coordinating between departments, and working collaboratively to meet production goals.
  • Working in improving production workflows, reducing downtime, and increasing yield.
  • Manage multiple projects and deadlines efficiently, ensuring timely production without compromising quality.
  • Preparing SOP, BMR, BPR and validation documents following GDP guideline.
  • Working in different validated software like QMS, LIMS, BME etc.
  • Performing qualification of different equipment.
  • Prepare and maintain production floor for facing audit & inspection.

Management trainee officer

Incepta Pharmaceuticals Ltd.
Dhaka
2019.09 - 2020.06
  • Perform physical and chemical tests of in-process materials, and finished products for quality testing following Good Laboratory Practices (GLP).
  • Maintain detailed records of all testing procedures, results, and deviations.
  • Perform laboratory equipment calibration and ensuring accurate and reliable results.
  • Participate in internal and external audits, ensuring the facility and practices are audit-ready.
  • Maintaining and enforcing protocols for handling hazardous materials and chemicals.

Education

Master of Science - Pharmaceutical Science and Drug Delivery Systems

London Metropolitan University
London
2024.09 -

Bachelor of Pharmacy - Pharmacy

University of Asia Pacific
Dhaka, Bangladesh
2015.04 - 2019.03

Skills

  • Strong verbal communication
  • Pharmaceutical manufacturing
  • Sterile compounding
  • Leadership and Teamwork
  • GDP, GLP and Data integrity
  • Audits and Inspections
  • Quality control testing
  • Regulatory compliance
  • QMS, LIMS, BME proficiency
  • Good manufacturing practice
  • Batch record reviewing
  • Risk assessment conducting
  • Laboratory equipment operation
  • Hazardous waste management
  • Laboratory safety protocols

References

References available upon request.

Timeline

Master of Science - Pharmaceutical Science and Drug Delivery Systems

London Metropolitan University
2024.09 -

Senior Production Pharmacist

Eskayef Pharmaceuticals Ltd.
2020.06 - 2024.08

Management trainee officer

Incepta Pharmaceuticals Ltd.
2019.09 - 2020.06

Bachelor of Pharmacy - Pharmacy

University of Asia Pacific
2015.04 - 2019.03
Mohammad Tanvir Hasan