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.
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
https://bdjobs.com/h/details/1535855
Category:Medical & Pharmaceuticals
Published:16 Sep 2026
Deadline:10 Oct 2026
Category:Medical & Pharmaceuticals
Published:16 Sep 2026
Deadline:10 Oct 2026
Category:Medical & Pharmaceuticals
Published:20 Sep 2026
Deadline:30 Sep 2026
Category:Medical & Pharmaceuticals
Published:20 Sep 2026
Deadline:30 Sep 2026