Kashab das Jiku

Kashab das jiku

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location of Kashab das JikuChattogram, Bangladesh
Followers of Kashab das Jiku823 followers
  • Timeline

  • About me

    Assistant Manager-Pharma at Reckitt ǁ Manufacturing ǁ FMCG ǁ Pharmacist ǁ Ex-GSK ǁ Ex-Square Pharmaceutical

  • Education

    • University of science & technology,chittagong.(ustc)

      2010 - 2011
      Master of pharmacy (m.pharm.) pharmacy
    • University of science & technology,chittagong.(ustc)

      2006 - 2009
      Bachelor of pharmacy (b.pharm.) pharmacy
  • Experience

    • Square pharmaceuticals

      Feb 2013 - Feb 2014
      Executive,quality complience

      Job Summary: To ensure that drug products are produced in SPL,pabna unit in accordance with the established procedures & condition which comply to the regulation of WHO cGMP standards & meet the specifications established by the company.Major Duties & Responsibilities:1.Monitor that routine batch manufacturing processes are being followed according to predefine guidelines as stated in the Batch Manufacturing Record(BMR) & Batch Packaging Record(BPR) in New Liquid manufacturing,MDI & general production areas including batch dispensing.2.Responsible to ensure manufacturing & packaging line clearance in New Liquid manufacturing,MDI,& general production areas.3.Monitor bulk & finished product IPC of New Liquid manufacturing MDI & general production areas & retention sample collection of those areas.4.Identitying constraintd of existing manufacturing,packaging & testing operation in compliance with cGMP & counseling with concerned personn in-site on root cause & find out the possible solution.5.Maintain discipline & favorable working environment in the organization & assist subordinates on technical matters. Show less

    • Square herbal and nutraceuticals ltd

      Feb 2014 - Jan 2016
      Executive,quality compliance

      Job Summary: To ensure that drug products are produced in SHNL in accordance with the established procedures & condition which comply to the regulation & meet the specifications established by the company.Major Duties & Responsibilities:1. Monitor that routine batch manufacturing processes are being followed according to pre- defined guidelines as stated in the Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR) of oral liquid, Capsules, Oral Powder & other products that are manufactured in SHNL Plant including batch dispensing of these dosage forms. 2. Responsible to ensure manufacturing and packaging line clearance in manufacturing of SHNL plant. 3. Monitor bulk and finished product IPC of Liquid, Capsules, Oral powder & other products in SHNL plant and ensure collection of Retention Sample from each batch of packed product. 4. Conduct visual cleaning inspection of processing areas and equipments to ensure that appropriate cleanliness is maintained according to relevant SOPs. 5. Identifying constraints of existing manufacturing, packaging and testing operations in compliance with cGMP and counseling with concerned personnel in-site on root cause(s) and find out the possible solutions.6. Preparation and revision of SOPs, Formats, Protocols and compilation of batch dossier.7. Maintain discipline & favorable working environment in the organization and assist subordinates on technical matters. 8. RM, PM & products analysis & release. Show less

    • Gsk

      Jul 2017 - Oct 2018
      Production officer

      Major Duties & Responsibilities:•Ensure & maintain quality at every stage of production according to cGMP, QMS, and SOP.•Implement the production plan to produce desired output through highest capacity utilization.•Ensure all the machine and equipment are regularly maintained for their highest performance.•Ensure good housekeeping.•Ensure all safety measures taken during product manufacturing and handling as and when required.•Carry out Quality & EHS L1 & L2 audit as per schedule.•Implementation of EHS Standards & Policies.•Implement operational excellence.•Ensure proper utilization of manpower.•Conduct Training Programme•Preparation and review of SOP•To ensure proper implementation of SOP, BMR & BPR•Ensure Departmental Risk Management and maintaining Risk Register.•To ensure proper PPEs are used and maintained by the employee’s•Any other job assigned by the manager. Show less

    • Reckitt

      Jul 2019 - now

      Job Summary:Responsible for Supervision, checking and ensuring overall Manufacturing and Packing activities of Pharma, DLS ,DBW & Trix units by ensuring Safety & Quality using different RPS tools.1.Ensure line wise OEE, productivity & Monthly target of for individual SKU's (Pharma, Trix,DLS,DBW) according to plan.2.Develop, ensure & review the Monthly in-house production plan based on S&OP demand and sales forecast for all sku’s in factory.3.Conducting training for new employees as well as refreshers training for existing staffs regarding the Safety Induction, EHS, process check, overall quality, SOP and cGMP.4.To maintain documentation such as URS, IQ, OQ, PQ and validation protocols with reports for new machineries.5..Prepare & Reviews of BMRs, BPRs, SOPs and formats along with QA department.6.Manpower handling, Continuous quality assurance, Production targets, EHS etc.7.Ensure overall RPS activity & using different RPS tools to improve productivity. Show less Job Summary:Responsible for Supervision, checking and ensuring overall Manufacturing and Packing activities of Pharma, DLS & Trix units by ensuring Safety & Quality. Major Duties & Responsibilities:1.Ensure all manufacturing (Pharma, DLS & Trix) posting in the JDE Edwards (ERP Software) on time as per production plan.2.Ensure line wise OEE, productivity & Monthly target of for individual SKU's (Pharma, Trix & DLS) according to plan3.Develop, ensure & review the Monthly in-house production plan based on S&OP demand and sales forecast for all sku’s in factory.4.Conducting training for new employees as well as refreshers training for existing staffs regarding the Safety Induction, EHS, process check, overall quality, SOP and cGMP.5.To maintain documentation such as URS, IQ, OQ, PQ and validation protocols with reports for new machineries.6.Prepare & Reviews of BMRs, BPRs, SOPs and formats along with QA department.7.Manpower handling, Continuous quality assurance, Production targets, EHS etc.8.Ensure cleanliness of hard to clean parts of equipment’s during cleaning for product -changeover and also to ensure cleaning between batch to batch of the same product.9.Preventive maintenance and calibration according to schedule with maintenance. Show less Job Summary:Responsible for Supervision, checking and ensuring overall Manufacturing and Packing activities of Pharma, DLS & Trix units by ensuring Safety & Quality. Major Duties & Responsibilities:1.Ensure all manufacturing (Pharma, DLS & Trix) posting in the JDE Edwards (ERP Software) on time as per production plan.2.Ensure line wise OEE, productivity & Monthly target of for individual SKU's (Pharma, Trix & DLS) according to plan3.Develop, ensure & review the Monthly in-house production plan based on S&OP demand and sales forecast for all sku’s in factory.4.Conducting training for new employees as well as refreshers training for existing staffs regarding the Safety Induction, EHS, process check, overall quality, SOP and cGMP.5.To maintain documentation such as URS, IQ, OQ, PQ and validation protocols with reports for new machineries.6.Prepare & Reviews of BMRs, BPRs, SOPs and formats along with QA department.7.Manpower handling, Continuous quality assurance, Production targets, EHS etc.8.Ensure cleanliness of hard to clean parts of equipment’s during cleaning for product -changeover and also to ensure cleaning between batch to batch of the same product.9.Preventive maintenance and calibration according to schedule with maintenance. Show less

      • Assistant Manager-Pharma

        Apr 2024 - now
      • Senior Production Officer

        Jul 2022 - Mar 2024
      • Production Officer

        Jul 2019 - Jun 2022
  • Licenses & Certifications