Job Summary
Sex type: Both
Job Nature:Full Time
Age:Na
Experience:1 to 2 yearsThe applicants should have experience in the following business area(s): Pharmaceutical/Medicine CompaniesFreshers are also encouraged to apply.
Educational Requirements: Bachelor of Pharmacy (B.Pharm)Master of Pharmacy (M.Pharm)B. Pharm/ M. Pharm from any reputed public/private University.
Salary Range: Negotiable
Published: 20 Sep 2026
Deadline: 30 Sep 2026
Vacancy: --
Job Description

Ziska Pharmaceuticals Limited, is one of the reputed pharmaceutical companies in Bangladesh. It is ISO 9001:2015 certified and has a fully GMP compliant factory which follows the USFDA guidelines. The phenomenal growth of Ziska Pharma offers suitable candidate not just a job but also the opportunity for rapid career growth. To support our rapidly expanding business, the company is looking for smart, ambitious, result-oriented & enthusiastic individuals for the positions

Job Location: Shofipur, Gazipur

Key Responsibilities:

  • Perform routine QA activities in production, warehouse, QC laboratory, and other GMP areas to ensure compliance with approved procedures and regulatory requirements.

  • Review and ensure compliance of batch manufacturing, packaging, and other relevant records before product release.

  • Perform line clearance, area clearance, and in-process checks during manufacturing and packaging operations.

  • Review and approve SOPs, specifications, batch records, protocols, reports, and other GMP-related documents.

  • Monitor and ensure compliance with GMP, GLP, GDP, data integrity, and company quality procedures.

  • Handle and review deviations, OOS/OOT, change controls, CAPA, market complaints, and non-conformities and ensure timely closure of assigned activities.

  • Conduct internal audits, self-inspections, and follow-up activities to identify gaps and ensure effective corrective actions.

  • Support validation and qualification activities, including process, cleaning, equipment, facility, utility, and computerized system validation.

  • Prepare and review Product Quality Reviews (PQR), quality reports, trend analysis, and other QA-related documents.

  • Ensure proper control and management of controlled documents, SOPs, logbooks, records, and other quality documents.

  • Coordinate with Production, QC, Warehouse, Engineering, and other departments to resolve quality issues and maintain continuous GMP compliance.

  • Support regulatory inspections, customer audits, and implementation of quality improvement initiatives within the organization.

Job Requirements

1 – 2 years of relevant experience in quality functions. Strong communication, collaboration skillsAnalytical Problem-solving and decision-making abilityIntegrity and continuous improvement mindsetMS-Office and report preparationAbility to work under pressure and manage multiple operational requirements

Job Source

https://bdjobs.com/h/details/1535855

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