Planning and Organizing to solve day to day technical issues related to Production and Formulation. Technical evaluation of Equipments related to Production , Process, Quality Control and Engineering.Planning and Designing of New Pharmaceutical Facility to comply cGMP. Coordinating the in-house team and vendor to complete the project within stipulated time and budget. Preparation of URS for new equipment necessary for the pharmaceuticals in respect to complying GMP requirements. Design Evaluation, Men-material flow logic, Cleanroom for sterile, aseptic products and for LVP., cleanroom for Ophthalmic products. Staff training and evaluation. Internal and self Inspection. Staff motivation and Productivity improvement.

Design Review, Contract to consultant, technical evaluation of Design and documents provided by consultant. Supervision of Product Development and document preparation. Project team management . Coordination and logistic support to the project team to complete the project timely within budget. Coordination to Bangladesh Drug Administration regulatory affair . Equipment selection , evaluation , conduct factory acceptance test of production and processing machine. SOP and other GMP documentation preparation and execution and review. Staff training. Technical meeting with the overseas technical team. Appraisal. Face GMP Audit. Conduct Self and Internal Inspection. CAPA.

Organizing planning production, processing, packaging. Product development, staff taring. Documentation. Annual product review. For ISO 9000-2001 program, I was management Representative.