Deputy General Manager / General Manager-Production

Job Summary
Sex type: Both
Job Nature:Full Time
Age:Na
Experience:At least 20 yearsThe applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Educational Requirements: M. Pharm from a reputed public/private university.
Job Location:Dhaka
Salary Range: --
Published: 14 Jul 2026
Deadline: 27 Jul 2026
Vacancy: --
Job Description

One of the top ten pharmaceutical companies is looking for an experienced Pharmacist for the position of Deputy General Manager/General Manager-Production at their Manufacturing unit. Qualified and interested professionals are highly encouraged to apply and explore this opportunity.

Major Duties and Responsibilities.

  • Lead, supervise, and control overall production operations of the solid dosage manufacturing facility, ensuring safe, efficient, and compliant operations.

  • Manage end-to-end manufacturing and packaging operations, including dispensing, granulation, blending, compression, encapsulation, coating, primary packaging, and secondary packaging, ensuring smooth execution in full compliance with approved SOPs, BMR/BPR, cGMP guidelines, and regulatory requirements.

  • Oversee production planning, scheduling, and capacity planning, ensuring optimum utilization of manpower, machines, materials, and other production resources to achieve production targets on time.

  • Drive productivity improvement, yield improvement, process optimization, waste reduction, and cost control initiatives to achieve operational excellence.

  • Monitor machine performance, equipment utilization, line efficiency, downtime, and production KPIs; coordinate maintenance and troubleshooting of production machinery and equipment.

  • Lead investigations into deviations, non-conformances, process failures, yield variation, product defects, and market complaints, ensuring timely and effective implementation of CAPA, change control, risk assessment, and continuous improvement actions.

  • Ensure proper GMP documentation (BMR, BPR, logbooks, status labels, equipment and cleaning records) and prepare the production facility and team to attend and support regulatory inspections by authorities such as DGDA, PIC/S, UK MHRA, WHO-GMP/EU GMP, ANVISA, TGA and other relevant regulatory bodies.

  • Support technology transfer, process validation, cleaning validation, qualification activities, and new product introduction as required.

  • Ensure effective coordination and collaboration with QA, QC, R&D, Warehouse, International Business, PMD, Supply Chain, Validation, Engineering, Regulatory Affairs, and other cross-functional departments.

  • Develop, train, coach, and motivate production team members to build a strong culture of health, safety, environment, quality, compliance, discipline, accountability, and operational excellence.

Job Location: Dhaka Division

Job Requirements

Minimum 20 years of practical experience in production operations of a reputed large pharmaceutical company.Practical experience in handling local and international regulatory audits is essential.Experience in facing audits by DGDA, PIC/S, UK MHRA, WHO-GMP/EU GMP, ANVISA, TGA, or similar stringent regulatory authorities will be highly preferred.

Job Source

https://bdjobs.com/h/details/1509496

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