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Assistant Manager- Quality Control

Job Description

Title: Assistant Manager- Quality Control

Company Name: Astra Biopharmaceuticals Ltd.

Vacancy: 1

Age: Na

Job Location: Dhaka, Dhaka (Ashulia), Mymensingh (Gouripur)

Salary: Negotiable

Experience:

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


Published: 2026-03-12

Application Deadline: 2026-04-11

Education:
    • Bachelor of Pharmacy (B.Pharm)
    • Master of Pharmacy (M.Pharm)
  • M.Pharm / B.Pharm / M.Sc in Chemistry or Applied Chemistry.



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


Skills Required:

Additional Requirements:
  • 6–8 years’ experience in QC in a pharmaceutical company.

  • The applicant should have experience in the following business area(s): Pharmaceutical/Medicine Companies

  • Must have registration under the Bangladesh pharmacy Council

  • Strong analytical and leadership skills.

  • Good communication and documentation ability.



Responsibilities & Context:

Company Overview

Astra Biopharmaceuticals Ltd. is a growing pharmaceutical company committed to providing high-quality, safe, and affordable medicines to improve healthcare standards in Bangladesh. The company follows international quality standards and modern manufacturing practices.

Job Responsibilities

  • Distribute daily jobs among junior colleagues and take feedback after completing the job.

  • Check different log books of QC laboratory are updated and Preparation of working standard and laboratory reagent as per procedure.

  • Monitor daily analysis of Raw material, Purified Water, in-process sample and finished product analysis.

  • Ensure instrumental calibration and validation for QC laboratory along with maintain qualification documents for existing instruments.

  • Able to prepare documents like machine operation and cleaning SOP, forms, Standard Test Procedures, Process validation related analysis, COA etc.

  • Lead the team for handling Out of Specification (OOS)/ Out of Trend (OOT) incidence with justification and maintaining proper documentation procedure.

  • Take initiative for analytical method validation/verification of different generics raw material and finished products.

  • Perform CAPA completion of QC department or other department if it is related with QC laboratory activity.



Job Other Benifits:
    • Attractive salary package (Negotiable)

    • Other benefits as per company policy.



Employment Status: Full Time

Job Work Place:

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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