Officer- Quality Control (Compliance & Validation)

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 sampling, testing, and inspection of raw materials, packaging materials, in-process, finished, stability, and retention samples as per approved specifications and SOPs.

• Conduct IPQC activities including dispensing, line clearance, status labeling, process monitoring, and changeover cleaning checks.

• Inspect production, warehouse, and QC areas to ensure compliance with GMP, GLP, SOPs, and required environmental conditions.

• Perform analytical testing using approved methods and ensure accurate documentation, review, and reporting of QC results.

• Maintain proper control of QC samples, laboratory records, instruments, logbooks, and other relevant documentation.

• Investigate and support the resolution of OOS/OOT, deviations, complaints, non-conformities, and CAPA related to quality activities.

• Prepare and review PQRs, QC reports, investigation reports, and other quality-related documents.

• Ensure compliance with GMP, ISO 9001, ISO 14001, data integrity, and applicable regulatory requirements.

• Plan, execute, and document equipment, facility, utility, process, cleaning, and computerized system qualification/validation activities.

• Prepare, review, and execute validation protocols and reports for DQ, IQ, OQ, and PQ, including revalidation and continued process verification.

• Support validation of critical utilities such as HVAC, purified water/WFI, compressed air, gases, and steam systems.

• Coordinate with QA, Production, Warehouse, Engineering, and other departments to resolve quality issues and ensure continuous compliance and improvement.

1 – 2 years of relevant experience in IPQC & Documentation and ValidationStrong 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/1535844

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