Executive - Quality Control

Job Description

Title: Executive - Quality Control

Company Name: Sun Pharmaceuticals (EZ) Limited

Vacancy: --

Age: 28 to 38 years

Job Location: Narayanganj

Salary: Negotiable

Experience:

  • 6 to 10 years


Published: 2026-07-26

Application Deadline: 2026-08-20

Education:

Requirements:
  • 6 to 10 years


Skills Required:

Additional Requirements:
  • Age 28 to 38 years


Responsibilities & Context:
  • Calibration Management:

  • Prepare and maintain the calibration schedule for all Quality Control laboratory instruments.

  • Perform calibration activities as per approved schedules, SOPs, and regulatory requirements.

  • Ensure proper documentation and timely review of calibration records.

  • Instrument Qualification & Maintenance:

  • Maintain qualification status (IQ/OQ/PQ) of all QC instruments.

  • Coordinate and ensure preventive maintenance of laboratory instruments as per schedule.

  • Maintain complete and compliant documentation related to qualification and maintenance activities.

  • Working Standard & Reference Standard Management:

  • Prepare and maintain the Working Standard (WS) schedule.

  • Prepare Working Standards as per approved SOPs and protocols.

  • Maintain and control all documentation related to Working Standards, CRS, and Impurity CRS, including usage, storage, validity, and reconciliation records.

  • Instrument Troubleshooting & Monitoring:

  • Perform troubleshooting and calibration of HPLC systems.

  • Monitor performance and ensure proper functioning of all QC laboratory instruments.

  • Escalate instrument-related issues and support corrective actions.

  • EDAMS / Data Management Activities:

  • Perform EDAMS-related activities for the Quality Control laboratory.

  • Ensure data accuracy, integrity, and compliance with applicable data integrity guidelines.

  • Regulatory & Departmental Support:

  • Carry out any other duties as assigned by superiors in support of departmental objectives, audit readiness, and regulatory compliance.

  • To Support internal and external audits by providing required documentation and explanations.

  • Compliance & Quality Responsibility:

  • Ensure all activities are conducted in compliance with cGMP, GLP, SOPs, and regulatory guidelines by Maintaining a high level of data integrity, documentation accuracy, and laboratory discipline.



Job Other Benifits:
  • Provident fund,Over time allowance,Gratuity,Insurance
  • Salary Review: Yearly
  • Lunch Facilities: Partially Subsidize
  • Festival Bonus: 2
  • LTA (Additional Bonus)



Employment Status: Full Time

Job Work Place: Work at office

Company Information:

Gender: Both 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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