Md. Isha Tareque

Experience

• 

  Eskayef Bangladesh Ltd.

  Jul 2004 - Dec 2009

  Production Pharmacist/ Sr. Production Pharmacist

  Worked as Production Pharmacist and Senior Production Pharmacist in Eskayef Bangladesh Ltd. And also perform active role to achieve MHRA accreditation.Be responsible for all the technical activities of Solid and Liquid Manufacturing Area as per GMP.Be responsible for the production planning concerning production program.Be responsible for that the awarded technical resources are used in a correct way and they always are in good condition.Be responsible for that the staffs under my jurisdiction are introduced and instructed in a good way to be able to fulfill their duties.To monitor, organize and document the intermediate bulk store, finished goods according to specified method.Be responsible for monthly statement and yearly auditBe responsible for the protection of the staff within the section concerning both chemical and mechanical risks and that all safety instructions are followed.Be responsible for the hygienic standard within the section.Be responsible for dispensing RM in FIFO basis following MO & BMR.Be responsible for all the batch records are filled in a correct way.Receive Raw materials and Packing materials as per MO and FO.Be responsible for that all equipment is cleaned in accordance with Cleaning instructions.Be responsible for productivity with quality.Be responsible for monthly statement and yearly audit.Be responsible for doing any other job assigned by Production Management.Be responsible for the preparation of documents like BMR, BPR and SOP.Be responsible for the management of RM store, PM store and FG store.Be responsible for the perfect utilization of Man-hour, equipment and facility. Show less

• 

  Healthcare Pharmaceuticals Limited

  Dec 2009 - Dec 2015

  Supervised all activities of the Cephalosporin production area including operation and planning of production, future expansion of facilities and improvement of productivity.Played important role in the design phase of Cephalosporin project in Healthcare Pharmaceuticals Ltd. Prepared URSs of major manufacturing machineries.Monitor that the staffs under my jurisdiction are introduced and instructed in a good way to be able to fulfill their duties.Monitor that the awarded technical resources are used in a correct way and they always are in good condition.Responsible for the protection of the staffs within the section concerning both chemical and mechanical risks and that all safety instructions are followed.Prepare daily, weekly, monthly, quarterly and yearly production plan based on marketing forecast and also monthly production statement and graphical presentation of comparison of productivity vs. capacity according to marketing forecast.Working as a member of “Validation & Documentation Team” to implement Process Validation, Equipment Qualification and Cleaning Validation.Engaged in the preparation and execution of Validation Documents like PQ Protocol and Reports. And establish Production SOPs, covering entire operation and their regular updating by incorporating changes where necessary.Carryout both routine and non-routine Validation & Documentation jobs in time to help smooth establishment of Quality Management System (QMS).Working in the implementation systems like Deviation and Deviation Report, Change Request and Change Request Report.Help Developing New Product with Product Development Dept. after formulae/manufacturing order authorization from Plant Head and QA Head.Arrange GMP training program for Production Personnel on different topics like Personnel Hygiene, Quality Housekeeping etc. as well as motivational training like Leadership training. Show less Supervised all activities of the Oral Solid manufacturing area including operation, planning, future expansion and improvement of productivity.Working as a member of “Validation & Documentation Team” to implement Process, Equipment and System Validation, including Cleaning Validation.Engaged in the preparation and execution of Validation Documents like IQ, OQ, PQ Protocol. And Reports.Carryout both routine and non-routine Validation & Documentation jobs in time to help smooth establishment of Quality Management System (QMS).Establish Production SOPs, covering entire operation and their regular updating by incorporating changes where necessary.Help Developing New Product with Product Development Dept. after formulae/manufacturing order authorization from Plant Head and QA Head.Arrange GMP training program for Production Personnel on different topics like Personnel Hygiene, Quality Housekeeping, Sterile Product, Processing, Water System, and HVAC system etc.Report Production activities to Production In-charge and to help to take decision in critical situation.Monitor that the staffs under my jurisdiction are introduced and instructed in a good way to be able to fulfill their duties.Prepare daily, weekly, monthly and quarterly production plan based on marketing forecast and also monthly production statement and graphical presentation of comparison of productivity vs. capacity according to marketing forecast.Keep close liaison with engineering department for day-to-day engineering problem.Responsible for the protection of the staffs within the section concerning both chemical and mechanical risks and that all safety instructions are followed.Help other Production Officer(s) when he/she is loaded with works. Show less

  • Assistant Manager, Production

    Jan 2014 - Dec 2015

  • Senior Executive

    Dec 2009 - Dec 2013
• 

  Beacon Pharmaceuticals PLC

  Aug 2016 - Aug 2023

  Supervise all activities of the Oral Liquid Facility including Operation, Planning, Future Expansion and Improvement of Productivity.Prepare Daily, Weekly, Monthly, Quarterly and Yearly Production Plan based on marketing forecast and also prepare Monthly Production Statement.Monitor Process Validation, Equipment Qualification and Cleaning Validation as a member of a multidisciplinary “Validation & Documentation Team”.Ensure process optimization either by introducing new ideas or by changing existing old system or facilities.Work closely with senior GMP consultants to implement their suggestion and observation in practice.Arrange GMP training program for Production Personnel on different topics like Personal Hygiene, Quality Housekeeping etc. as well as motivational training like Leadership& QCC training.Successfully completed Qualification of all Production Machineries, including the Qualification of Water and HVAC system of the Oral Liquid Project. Also successfully completed the Technology Transfer from the toll side.As additional job responsibility, prepared Equipment Foot Print Layout, Room Data Sheet, Qualification Documents (URS, DQ, IQ, OQ & PQ) of all Process Equipment, Cleaning Validation Protocol of Cephalosporin Project. Show less

  • Production Manager

    Jan 2022 - Aug 2023

  • Deputy Manager Production

    Aug 2016 - Dec 2021