Executive, Quality Operations (QA, QC)

Job Description

Title: Executive, Quality Operations (QA, QC)

Company Name: Popular Pharmaceuticals PLC.

Vacancy: --

Age: At most 32 years

Job Location: Gazipur (Tongi)

Salary: Negotiable

Experience:

  • At most 2 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
  • Freshers are also encouraged to apply.


Published: 2026-09-09

Application Deadline: 2026-09-19

Education:
    • Master of Pharmacy (M.Pharm)
    • Master of Science (MSc) in Chemistry, Applied Chemistry, Biochemistry


Requirements:
  • At most 2 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
  • Freshers are also encouraged to apply.


Skills Required:

Additional Requirements:
  • Age At most 32 years
  • Good proficiency in MS Office with basic knowledge of GMP, GLP, SOPs, and pharmaceutical quality standards

  • Strong analytical, problem-solving, and decision-making skills

  • Proactive, positive, responsible, and detail-oriented attitude

  • Good communication and teamwork skills, with sincerity, honesty, and professional integrity



Responsibilities & Context:

Popular Pharmaceuticals PLC is a leading pharmaceutical company in Bangladesh, with a state-of-the-art manufacturing facility in Tongi, Gazipur, around 10,000 employees, and exports to 34 countries worldwide.

Ready to make an impact? Join our winning team and grow with a company driven by innovation, excellence, and global ambition.

Job Description:

  • Implement, monitor, and ensure compliance with applicable GMP requirements, SOPs, and established quality standards.

  • Ensure proper documentation, change control, deviation management, risk assessment, and other quality management processes in accordance with company procedures and regulatory requirements.

  • Support regulatory inspections, internal and external audits, and ensure timely implementation of corrective and preventive actions (CAPA).

  • Conduct and review testing of raw materials, packaging materials, in-process samples, and finished products in accordance with approved specifications and analytical procedures.

  • Execute and monitor stability studies and support analytical method validation/verification activities as per approved protocols and regulatory requirements.

  • Ensure laboratory operations comply with GLP, safety requirements, data integrity principles, and applicable regulatory standards.

  • Collaborate with Production, R&D, and other relevant functions to investigate and resolve quality-related issues and support continuous improvement initiatives.

  • Perform any other duties and responsibilities assigned by the Supervisor/Management from time to time.



Job Other Benifits:
    • Provident Fund

    • Gratuity

    • Festival Bonus: 3 (Yearly)

    • Earn Leave Encashment

    • Leave Fare Assistance

    • Profit Bonus

    • Weekly holiday: 2 days

    • Pick & drop facility

    • Group Life Insurance

    • Subsidized lunch facility



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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