Assistant QC Manager

Job Description

Title: Assistant QC Manager

Company Name: M/s Super Power Pharmaceuticals Ltd.

Vacancy: 02

Age: Na

Job Location: Narsingdi (Belabo)

Salary: Negotiable

Experience:

  • 4 to 5 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies


Published: 2026-02-17

Application Deadline: 2026-03-19

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

  • Candidate must have computer skill & well conversant with Microsoft Office applications.

  • Candidate should have registration number given by Bangladesh Pharmacy Council (In case of Graduate Pharmacist).



Requirements:
  • 4 to 5 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies


Skills Required: Quality assurance and control,Quality Control

Additional Requirements:

Candidate should have profound knowledge on Standard Operating Procedure (SOP), Pharmaceutical Analysis, Pharmaceutical Calibration/Validation, Process Validation, Proper Documentations, Regulatory Affairs etc. Candidate should be skilled on HPLC, FTIR, UV, ASS, GC, TLC & others QC Equipment’s. Enable to prepare MOA, COA, Method Verifications and Specifications, Method Validations. Coordinate pharmaceutical-related activities for all products.



Responsibilities & Context:
  • Support regulatory inspections and compliance audits.

  • Oversee daily testing operations, including the analysis of raw materials, in-process samples, and finished products using advanced instruments like HPLC, GC, UV, and FTIR.

  • Ensure all lab activities strictly adhere to cGMP (current Good Manufacturing Practices) and GLP (Good Laboratory Practices) guidelines.

  • Review and approve Standard Operating Procedures (SOPs), batch records, and analytical reports to ensure data integrity and traceability.

  • Lead investigations into Out of Specification (OOS), Out of Trend (OOT), and deviations, identifying root causes and implementing CAPA (Corrective and Preventive Actions).

  • Organize and monitor the calibration of QC instruments and the validation of analytical methods to ensure high precision.

  • Participate in and prepare the department for internal audits and external inspections from regulatory bodies like the local drug administrations (DGDA).

  • Manage stability testing programs to determine the shelf-life and storage conditions of various drug formulations

  • Performs other duties as assigned by QC/QA Manager & Plant Manager/In charge.



Job Other Benifits:
  • Salary Review: Yearly
  • Festival Bonus: 2
    • Salary & other benefits will be considered as per company rules & policies.

    • Special preference will be given to the candidates who have practical knowledge & experience in launching injectable/Sterile Products and attractive salary will be offered to such candidates.



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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