Md. Shariful Islam

Experience

• 

  Beximco Pharmaceuticals Ltd.

  Jan 2008 - Dec 2009

  Production Officer

  1. To ensure line clearance before execution of any manufacturing step, proper labeling, logbook update.2. To develop and ensure right packaging materials and information materials of finished drugs products.3. To ensure proper storage of in-process and finished drug products.4. To monitor, follow-up and co-ordinate routine environmental monitoring studies.5. To plan, organize and carryout cleaning validation activities and necessary documentation.6. To ensure preparation and routine revision of necessary GMP documents.7. To ensure and conduct required training for relevant staff.8. To ensure adequate housekeeping, personnel and product safety. Show less

• 

  Square Pharmaceuticals Limited

  Jan 2010 - Nov 2015

  Production Executive and senior Production Executive

  1. To plan, co-ordinate and carry out production operation in term of output, quality, cost, available time and labor requirements to ensure continuous supply of products.2. To co-ordinate and participate in formulation development of new drug products.3. To ensure stability study and hold time study of newly formulated drug products.4. To plan and execute scale up and commercial manufacturing of newly formulated drug products.5. To carryout process optimization and process validation of newly formulated drug products in production facility.6. Commercial manufacturing, troubleshooting and scale up of existing drug products.7. To ensure all quality parameters including efficacy, potency, integrity and purity of drug products both in in-process stages and finished products.8. To ensure cGMP and GDP in every stage of manufacturing and packaging operations following necessary regulatory guidelines.9. To ensure line clearance before execution of any manufacturing step, proper labeling, logbook update.10. To develop and ensure right packaging materials and information materials of finished drugs products.11. To ensure proper storage of in-process and finished drug products.12. To monitor, follow-up and co-ordinate routine environmental monitoring studies.13. To plan, organize and carryout cleaning validation activities and necessary documentation.14. To ensure preparation and routine revision of necessary GMP documents.15. To ensure and conduct required training for relevant staff.16. To ensure adequate housekeeping, personnel and product safety.17. To report deviation and ensure change control before execution of any change.18. To participate and co-ordinate investigation against deviation and market complaint, recommendation of CAPA, their implementation, follow up.19. To ensure qualification of existing and new machines (IQ, OQ, PO).20. To prepare production report, analyze capacity utilization of existing facilities and plan for future expansion Show less

• 

  NIPRO JMI PHARMA

  Dec 2015 - Mar 2020

  Deputy Manager

  Major Responsibilities:1. To plan, co-ordinate, conduct and actively participate in the manufacturing of newly formulated drug products, process optimization and process validation in his area of responsibilities.2. Commercial manufacturing, troubleshooting and scale up of existing drug products manufactured in General Production Unit.3. To ensure quality of drug products manufactured under his supervision (including all quality parameters of both in-process and finished products ensuring efficacy, strength, integrity and purity of drug products).4. To maintain cGMP and GDP standard following the international and local regulatory requirements in the manufacturing and packaging area.5. To ensure work place safety and legal safety requirements within the production area.6. To monitor, follow-up and co-ordinate routine environmental monitoring, cross-contamination studies and cleaning validation activities.7. To ensure adequate training of process personnel on process and procedures.8. To raise change control, report deviation on timely fashion, participate in investigation, and implement appropriate recommendation CAPA and follow-up effectiveness of CAPA.9. To co-ordinate internal and external inspection in production area, follow-up inspection report, implement the required CAPA.10. To execute and follow up actions related to OOS, stability study, market complaint, deviation and inspection findings in order to ensure safety and efficacy of drug products.11. Production planning and execution all routine production activities and assist Production Manager.12. To co-ordinate and carry out machine qualification including FAT, IQ, OQ and PQ activities.13. To execute and follow up actions related to OOS, stability study, market complaint, deviation and inspection findings in order to ensure safety and efficacy of drug products.14. Any other tasks assigned by higher management when required. Show less

• 

  SHARIF PHARMACEUTICALS LIMITED

  Mar 2020 - Jan 2024

  Production Manager
• 

  BEXTER PHARMACEUTICALS

  Feb 2024 - now

  Production Manager