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BEXIMCO PHARMACEUTICALS LIMITED
TONGI - 1711, GAZIPUR, BANGLADESH
JOB DESCRIPTION
Name of the employee: Md. Khalid Hossain
Qualification: MBA, M.Sc. (Biochemistry) Designation: Assistant Manager,QA
Department: Quality Assurance Experience: 08 years and 08 Months
Date of Joining: 31/08/2006 Employee code: 08593
Reporting To: Executive Director, Quality Span of Control: Nil
Responsibility
 To monitoring of GMP at various stages of Production to meet the regulatory requirements.
 Online review of Batch Production records.
 Conduct training for incumbent of QA department related to IPQA system.
 To check temperature, Humidity & Pressure differential records/charts and other operational
records in production area.
 In-process inspection, line clearance and sampling of products (Intermediate and Finished stage).
 Operational support & co-ordination to IPQA activities, process validation, cleaning validation &
any other validation, relevant SOPs meeting cGMP and regulatory requirements.
 Requisition and management of inventory and other necessary support to maintain the GDP of QA
department.
 Analysis of in-process quality assurance sample.
 To check proper labeling of the product container and status labeling of equipment and area.
 Preparation of calibration master list, calibration master plan before beginning of each year and
when required.
 Calibration of all IPQA instruments as per Calibration Master Plan.
 Preparation of QA SOPs, Calibration Master Plan, In-process Sampling Plan etc.
 Ensure the update of all IPQA specifications, sampling plan & ensure supply of all IPQA
intermediate, finished, control & stability sample to QC on time.
 Any additional responsibilities as per the work requirement of the department from time to time.
I accept
Name/Signature Date :
Head of Department
FRM No.: FTR/002-03

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Job Description (KHD)

  • 1. BEXIMCO PHARMACEUTICALS LIMITED TONGI - 1711, GAZIPUR, BANGLADESH JOB DESCRIPTION Name of the employee: Md. Khalid Hossain Qualification: MBA, M.Sc. (Biochemistry) Designation: Assistant Manager,QA Department: Quality Assurance Experience: 08 years and 08 Months Date of Joining: 31/08/2006 Employee code: 08593 Reporting To: Executive Director, Quality Span of Control: Nil Responsibility  To monitoring of GMP at various stages of Production to meet the regulatory requirements.  Online review of Batch Production records.  Conduct training for incumbent of QA department related to IPQA system.  To check temperature, Humidity & Pressure differential records/charts and other operational records in production area.  In-process inspection, line clearance and sampling of products (Intermediate and Finished stage).  Operational support & co-ordination to IPQA activities, process validation, cleaning validation & any other validation, relevant SOPs meeting cGMP and regulatory requirements.  Requisition and management of inventory and other necessary support to maintain the GDP of QA department.  Analysis of in-process quality assurance sample.  To check proper labeling of the product container and status labeling of equipment and area.  Preparation of calibration master list, calibration master plan before beginning of each year and when required.  Calibration of all IPQA instruments as per Calibration Master Plan.  Preparation of QA SOPs, Calibration Master Plan, In-process Sampling Plan etc.  Ensure the update of all IPQA specifications, sampling plan & ensure supply of all IPQA intermediate, finished, control & stability sample to QC on time.  Any additional responsibilities as per the work requirement of the department from time to time. I accept Name/Signature Date : Head of Department FRM No.: FTR/002-03