Executive/ Sr. Executive, Quality Assurance

Job Description

Title: Executive/ Sr. Executive, Quality Assurance

Company Name: One Pharma Limited

Vacancy: 1

Age: At most 30 years

Job Location: Bogura

Salary: Negotiable

Experience:

  • At least 3 years


Published: 2026-05-06

Application Deadline: 2026-05-31

Education:
  • B. Pharm/ M. Pharm from any reputed University.



Requirements:
  • At least 3 years


Skills Required:

Additional Requirements:
  • Age At most 30 years
  • At least 3 - 5 years of experience in Pharmaceutical Quality Assurance Department.

  • Practical experience in production/QA activity.

  • Must have computer knowledge (MS Word, Excel).

  • Quick decision-making and problem-solving capabilities.

  • Proactive, Smart and positive attitude.



Responsibilities & Context:

Context:

One Pharma Ltd. embarked on its pioneering journey in November 2015 with a focus on incorporating cutting-edge manufacturing technology and producing globally acclaimed pharmaceutical products for the patients of Bangladesh and beyond. One Pharma Limited is looking for some experienced, reliable, honest & dedicated candidate for the position of Executive/ Senior Executive, Quality Assurance department for its factory (BSCIC, Bogura).

Job Responsibilities:

  • Ensuring line clearance for all processing stages of manufacturing & packaging operations (i.e. Dispensing, granulation, blending, compression, coating, Encapsulation, Liquid processing & filling-sealing, PFS filling-sealing, primary and secondary packaging) and perform In process Quality Assurance check to ensure the compliance .

  • Dossier Preparation.

  • Step wise BMR & BPR Review to ensure the completeness of document.

  • Arrange batch release after evaluation of all batch documents for distribution & sale at toll site .

  • Sampling of Intermediate, Bulk & Finished products.

  • Retention sample management

  • To prepare and update SOP’s & EOP’s related to QA and others department.

  • Investigation of Non conformances.

  • Investigate customer complaints in order to identify the root cause.

  • Handling of Deviation. 

  • Handling of Return goods.

  • Change control Management

  • Archive, storage, retrieval, disposal of Records and documents.

  • APQR Preparation

  • Participation in Process Validation, Equipment Qualification activities.

  • Ensuring the implementation of CAPA recommendation.

  • Ensure proper monitoring to avoid cross contamination.

  • Any other tasks assigned as & when required.



Job Other Benifits:
  • Provident fund,Mobile bill,Over time allowance
  • Lunch Facilities: Partially Subsidize
  • Salary Review: Yearly
  • Festival Bonus: 2


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: Production/Operation

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