Md. Enamul Hasan

Md. Enamul Hasan

In-Plant Trainee

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  • Timeline

  • About me

    Quality Compliance Officer at ACI Pharmaceuticals Ltd.

  • Education

    • Govt. K. C. College, Jhenidah-7300, Bangladesh.

      2014 - 2016
      H.S.C. Science GPA: A (4:67 out 5.00)
    • Khalishpur Secondary School

      2009 - 2014
      S.S.C. Science A+ (GPA: 5:00 out of 5:00)
    • Noakhali Science and Technology University

      2021 - 2022
      Master of Science - MS Applied Chemistry and Chemical Engineering First Class (CGPA: 3.34 out of 4.00)

      Major modules: Pharmaceutical Technology | Chemical Engineering | Environmental Chemistry and Pollution Control | Biodegradable Polymer.

    • Noakhali Science and Technology University

      2017 - 2022
      Bachelor of Science - BSc Applied Chemistry and Chemical Engineering First Class (CGPA: 3.20 out of 4.00)

      Major modules: Instrumental Method of Analysis | Analytical Chemistry | Chemical Technology | Chemical Engineering | Pharmaceutical Process and Technology | Organic Chemistry | Environmental Chemistry| Fuel Technology| Material Science and Engineering.

  • Experience

    • Globe Pharmaceutical Group of Companies Ltd

      Feb 2021 - Mar 2021
      In-Plant Trainee
    • Training Institute for Chemical Industries (TICI)

      Mar 2021 - Apr 2021
      Industrial Trainee

      I have successfully completed the course named " Industrial Process Unit Operation & Process Control Technique" and obtained grade A+ in the final evaluation.

    • ACI Limited

      Jun 2023 - now
      Quality Compliance Officer

      (a) Daily In process inspection and other activities:1. Cleaning clearance (Room, machine, Line, Area, Tools, Equipment etc.)2. Change over clearance (Mfg and packing area)3. Labeling work for maintaining segregation in various stages quarantine/ release etc.4. Environmental clearance (Temperature, Humidity, pressure diff.)5. Dispensing(solid, liquid, injectables)6. Liaison /communication with QC for arranging release label.7. IPC analytical tests8. Performing daily calibration of IPC instruments.9. Compression clearance10. Intermediate and bulk and finished product clearance 11. Clearance of preparatory work for injection items(autoclave, de-pyrogenation, filter integrity, particle count, pH meter check, balance performance etc.)12. In process during manufacturing (covering 3 times each batch)13. In process during packing (covering 3 times each batch)14. Sample collection (chemical, microbiological, visual and Retention, Real time & Validation)15. Final check of finished production before dispatch into WH.16. Documentation work related in process inspection17. Reporting of non compliance issues through mailing/pictorial presentation.18. Attaching ‘release label for sale’ in finished warehouse (b) Documentation work and other activities:1. Preparation of Monthly in-process inspection report2. NCR handling activities and reporting3. Deviation investigation and reporting 4. Annual Product Quality Review(APQR)5. Change Control review and related activities6. Customer Complaint investigation and reporting 7. Training Management 8. Checking of Retention Samples and reporting 9. Performing vendor audit and reporting10. Preparation/revision of SOP11. Self inspection/internal audit and reporting12. Refurbishing activates(Depot/Factory) 13. Destruction and write off activates 14. Validation activities(HVAC, autoclave, oven) Show less

  • Licenses & Certifications

    • In-Plant Training

      Globe Pharmaceutical Group of Companies Ltd
      Feb 2021
    • Industrial Process Unit Operation and Process Control Technique

      Training Institute for Chemical Industries (TICI)
      Apr 2021
    • Excel Skills for Business: Essentials

      Coursera
      Oct 2020
      View certificate certificate