Deputy Manager - Quality Control Department

Job Description

Title: Deputy Manager - Quality Control Department

Company Name: Al SAFA Pharmaceuticals

Vacancy: 1

Age: At least 38 years

Job Location: Gazipur

Salary: Negotiable

Experience:

  • 8 to 12 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Medical Equipment


Published: 2024-12-21

Application Deadline: 2024-12-31

Education:
    • Master of Pharmacy (M.Pharm) in Chemistry
    • Bachelor of Pharmacy (B.Pharm) in Chemistry
  • B. Sc. in Chemistry/Applied Chemistry/Biochemistry (From reputed Universities)



Requirements:
  • 8 to 12 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Medical Equipment


Skills Required: Pharmaceutical Product Management,Pharmaceutical Production,Pharmaceuticals

Additional Requirements:
  • Age At least 38 years


Responsibilities & Context:
  • Responsible to prepare, approve and review all QC documents like Standard Operating Procedures (SOPs) for analysis of incoming raw and packaging material, analysis of specimen sample for source approval, in-process materials analysis, finished goods analysis, QC Laboratory equipment operation and cleaning procedure.

  • Distribute daily jobs to the QC Officers and provide them supports like necessary SOPs for analysis, monitor their activity and to guide them to complete their job accurately in time.

  • Review the test results produced by QC Officers against specification and make decision on approval or repetition of the test or rejection of the sample.

  • Monitor the analytical method validation program in QC Laboratory. Actively participate to develop any cost effective analytical method and validation of this method.

  • Provide training to QC personnel on QC activity, techniques to increase their potentiality and on QC related theoretical knowledge.

  • Monitor the calibration and maintenance activity of QC laboratory equipment done as per schedule.

  • Maintain GLP and housekeeping in the C laboratory and implement corrective measure for any deviation.

  • Participate in investigation activity against any unwanted incidence.

  • Evaluate and review the performance assessment of the junior colleagues of QC department.

  • Develop the junior colleague of QC department so that in emergency situation he can run the activity consulting with head of QA department.

  • Reduce the time of analysis and testing of finished products and raw materials by developing technical methods and also preparing alternative method in a cost effective way.



Job Other Benifits:

    As Per Company policy.



Employment Status: Full Time

Job Work Place: Work at office

Company Information:

Gender: Male and Female can apply

Read Before Apply: Please apply only who are fulfilling all the requirements of this job

Category: Pharmaceutical

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