Production Operations
End-to-end production from raw material dispensing through finished-product packaging.
Production Manager · Operational Excellence · GMP & Quality Leadership
A pharmaceutical production professional with 16+ years of experience across production and quality assurance, combining manufacturing expertise, regulatory discipline, process optimization and people leadership.

I lead pharmaceutical production with a practical balance of business delivery, regulatory compliance and workforce performance.
My background spans end-to-end manufacturing operations, production planning, GMP and quality standards, machinery qualification, documentation, risk management, CAPA, budgeting and cross-shift team leadership.
My career objective is to contribute in senior pharmaceutical production leadership where operational excellence, manufacturing expertise and people management directly support sustainable organizational growth.
Production schedules, performance monitoring, documentation and control.
GMP, audits, inspections, CAPA, SOP/BMR/BPR and quality systems.
Manpower planning, coaching, evaluation, training and industrial relations.
Capacity expansion, productivity improvement and process optimization.
End-to-end production from raw material dispensing through finished-product packaging.
Production schedules, capacity planning, performance reporting and annual budgeting.
Quality standards, regulatory requirements, audit readiness and controlled documentation.
Productivity improvement, manpower optimization, risk management and CAPA initiatives.
URS, TSR, commercial specifications, machinery selection, qualification and FAT support.
Multi-shift supervision, training, delegation, performance management and industrial relations.
Operational reporting and enterprise-system discipline supporting production visibility.
In-process controls, batch reconciliation, process verification and continuous compliance.
Leading end-to-end production operations, schedules, multi-shift teams, GMP compliance, equipment procurement specifications, qualification, documentation, budgeting, CAPA, risk management and people development.
Progressed into broader production leadership and supported major scale-up, productivity and manufacturing-line initiatives.
Managed manufacturing and packaging of Cephalosporin products, production planning, material control, in-process quality, reconciliation, productivity tracking and regulatory audits.
Prepared export dossiers and regulatory documents for 28+ international markets while supporting in-process quality control, final inspection and GMP process verification.
Expanded production capability at SMC Enterprise Ltd.
Operational improvement through workforce and process focus.
Workforce optimization at SMC Enterprise Ltd.
New-line capability established in 2020.
Supported facility establishment at The Acme Laboratories Ltd.
International-market documentation during early career.
University of Development Alternative (UODA)
CGPA 3.60Khulna University
CGPA 3.14Bangladesh Skill Bank · 1 Year
Business & ManagementProfessional development spanning AI for business, finance, labor law, ISO quality systems, negotiation, leadership communication, project management and GMP practice.
My approach is to create clarity around standards, ownership around execution and measurable improvement around capacity, productivity and compliance.
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For professional discussions around pharmaceutical manufacturing, production leadership, operational excellence and organizational growth.