Mijanur Rahman

• Review and approve analytical reports (RM, PM, Bulk & FG).
• Authorize finished product release based on compliance.
• Conduct reagent preparation and standardization.
• Lead investigations for non-conforming products.
• Implement CAPA and continuous improvement initiatives.
• Ensure GMP, hygiene, pest control, and regulatory compliance.
• Maintain controlled documentation and laboratory records.

• Verified analytical reports and ensured product compliance.
• Conducted retention sample testing and reporting.
• Prepared rejection investigation reports.
• Coordinated laboratory calibration and safety drills.

• Performed RM, PM, FG sampling and laboratory analysis.
• Ensured ISO compliance and documentation control.
• Managed non-conforming materials and rework processes.

• Monitored production processes and in-process QC.
• Ensured defect-free production for local & export markets.
• Verified labeling, coding, and packaging compliance.

• Conducted quantitative analysis of RM & FG.
• Maintained sanitation and GMP standards.
• Monitored pre, in-process and post-production quality.