Rajib Bhowmik

Results-driven planning and operations management professional with exceptional communication, problem solving, leadership skills & project planning. Focused on developing a healthcare system that meet people expectation and have a global impact on digital healthcare management.

• Selected and worked as a SME (Subject matter expert) by the GSK authority for taking active participation in the Remediation exit plan & QIP (Quality Improvement Plan) project.
• Investigate and implement ideas for quality improvement, increased productivity and cost reduction through CIF (Continues Improvement Framework) and Operational excellence by increasing OEE (Overall equipment effectiveness) of packing line (55% to 64%), OT reduction (35% from previous year) and Batch size optimization.
• Implemented six different standards of GPS (GSK Production system) to ensure zero waste, zero defect and zero accident. (Reduced OPEX by 15% compared to last year).
• Perform General risk assessment, CRA (Chemical risk assessment) and Ergonomic risk assessment for routine activity, FMEA (Failure mode effect analysis) and Method statement for non-routine activity.

• Debate
• Sports (Cricket and Badminton)
• Event organizing capability
• Travelling

• Plant Manager, 3 years, Royal Pharmaceuticals Ltd, Chittagong, Production/ Operation Management (1 yr), Project Management (2 yrs), Audit readiness for any kind of GMP or regulatory audit., Make the project ready for operation., Preparing URS for purchasing new equipments and instruments., Preparation of annual budget plan and CAPEX., Production plan and execution., Operation expenditure reduction., Lead all the sections (production, Engineering, QA, QC, PD, Warehouse etc.) with dynamic decisions and strong leadership., Vendor selection & Dealing with the external supplier., Sourcing of RM, PM and required equipment., Launching activity of new generics., Facility expansion plan and execution.
• Deputy Manager, 0.8 year, Healthcare Pharmaceuticals Ltd, Gazipur, Leading the Production & QA team in right direction, SOP review and revision as per standard guideline, Preparation of Site Master File & Quality Manual and Training Manual, Implementation of Self Inspection/Internal Quality Audit, Deviation management & Change control management., Manage product quality to guarantee compliance with quality policies, procedures and systems. Identify QMS gap with analysis., Ensure readiness for DGDA audit and other external audit., Management & closing activity of CAPA and JDI which are generated from different audits and risk assessments., Perform six steps RCA & Investigation, Proper handling of market complaints., Process Validation and protocol preparation., Data integrity practitioner., Risk Management and risk assessment, Training management
• Senior Officer, Production (Grade-2) / (Eqv to Asst Manager), 4.4 years, GlaxoSmithKline Bangladesh Ltd, Chittagong, Cephalosporin, Topical (Cream & Ointment), Successfully managed production activities to adhere with weekly and monthly CTP., Investigate and implement ideas for quality improvement, increased productivity and cost reduction through CIF (Continues Improvement Framework) and Operational excellence., Manage documentation and training on production procedures and work instructions., Procurement of required manufacturing equipment and parts through ERP system., Plan, direct, coordinate and assign manpower to meet aggressive production schedules., Perform sectional KPI management through daily TIER meeting., Define manufacturing performance standards and review the outcome of performance goals to set future targets., Perform General risk assessment, CRA (Chemical risk assessment) and Ergonomic risk assessment for routine activity, FMEA and Method statement for non-routine activity., Drove daily production activities with effective communication and leadership., Direct improvements in process safety by implementation of LOTO, PTW and PPE’s., Manage product quality to guarantee compliance with quality policies, procedures and systems. Identify QMS gap with analysis., Escalate safety and quality issues and initiate remedial actions promptly. e.g: ZAP reporting., Perform L-1, L-2 Audit & ensure audit readiness for L-3 & L-4 audit., Management & closing activity of CAPA and JDI which are generated from different audits and risk assessments., Use six different standards for GPS (GSK Production system) to ensure zero waste, zero defect and zero accident., Perform six steps RCA & Investigation for Deviation & Change control management., To prepare the SOP’s and instructions for the production floor and ensure timely review., To take part in process validation., Use of different software, e.g: QWF, CERPS, BPCS, CDMS, CMMS etc., Analysis monthly Man Hour Utilization & Finding the root cause of variation.
• Senior. Production Officer, 1.8 years, ACI Ltd, Narayangonj, Pharmacist (1.8 yrs), Co ordinate the whole solid manufacturing section., To design the production plan and organize the production activities according to the production plan., To prepare the daily and monthly production report., To increase the productivity by the highest utilization of man & machine., To maintain the GMP into the production area., To initiate the regulatory guidelines into the production area., Troubleshooting during the production (if any)., To keep and maintain all kinds of documentary work., Preparation of SOP`s and instructions for GMP., To maintain discipline into the section.
• Production Officer, 2.1 years, ACI Limited, Narayangonj, To ensure GMP in all area of production., To handle the manpower for timely production., To increase the productivity by proper utilization of man & machine., To produce the product according to ROFO , DPP & MPP., To take necessary action when there is any difficulties or any problem in the production., To take part in process validation.
• Product Development Officer, 1 year, Silva Pharmaceuticals Ltd, Maijdee, Noakhali, Formulation, Carry on /Monitor trial, pilot batch production as per new formulation, Establish new formulation by process validation of minimum three consecutive batches & its report., To prepare & establish the Pilot Batch Manufacturing sheets & records before commercial production and analyze the physico-chemical test parameters of raw materials, packaging materials & finished products., Handle primary QC instruments including UV-Visible spectrophotometer., Proper handling of market complaints., Implement the accelerated & real time stability study of new molecules & existing product., Establish & review raw materials source validation., Review old formulations to minimize production cost as well as set the quality parameters within the limit., Design and establish new formulation of pharmaceutical dosage form., To prepare technical data sheet and annexure of pharmaceutical dosage form., To prepare necessary documents, forms and records of new products related to pre-registration/ inclusion to Drug Administration., To validate the existing process for better output/ productivity., Analysis of specimen sample (raw & packaging goods) and report these accordingly in time., Keep and maintain all records accordingly in the register files.

• Royal Pharmaceuticals Ltd, Project In Charge, 3 years, Project Operation, Chittagong
• Healthcare Pharmaceuticals Ltd, Deputy Manager, Production, 0.8 year, Overall Production, Gazipur
• GlaxoSmithKline Bangladesh Ltd, Senior Officer, Production (G-1) & Senior Officer, Production (G-2) (Equv. to Asst Manager), 4.4 years, Cephalosporin, Topical (Cream & Ointment), Chittagong
• ACI Limited, Senior Production Officer & Production Officer, 4 years, Solid (Tablet, Capsule, Dry syrup), Narayangonj
• Silva Pharmaceuticals Ltd, Product Development Officer, 1 year, Formulation, Maijdee, Noakhali

• Junior Scholarship-1997
• B.S.C scholarship - 2003, offered by NIPPON FOUNDATION-JAPAN.

• ID Number: 1920522412
• Total Experience: 13.7 years
• Passport Number: A11269899
• Blood Group: O (- ve)
• Date of birth: 07/15/85
• Marital status: Married
• Religion: Hindu

• Nakibur Rahman, Country Manager, Novartis Bangladesh Ltd, 01713-174050
• Mr Omar Faroque, General Manager, Production, ACI Limited, 01714 - 092743

• EDM (Excellence in deviation management), 1 week, GSK global expert
• PCCE (Physical contamination cause and elimination) through FMEA (Failure Mode Effect Analysis), 1 week, GSK global expert, True
• TQM (Total Quality Management), 3 days, HIDA & GSK, True
• FLL (First line leadership), 2 days classroom + 6 months online, GSK
• EHS, QMS & LSOP, More than 300 online trainings
• GPS (GSK Production System), Training
• GMP training, 7 days, Cleaning Validation, Site Master Plan, Change Control, Process Control, People & Dept Development, Mr Wayne McKenzie, Pharmaceutical Specialist Trainer, Asia Pacific Consultants Pvt Ltd, Australia
• Handling of Customer Compliance, 1 Day

Registered Pharmacist (A Grade)