Officer- Quality Assurance

Job Description

Title: Officer- Quality Assurance

Company Name: Ziska Pharmaceuticals Ltd.

Vacancy: --

Age: At least 25 years

Job Location: Gazipur

Salary: Negotiable

Experience:

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

• Bachelor of Pharmacy (B.Pharm)
• Master of Pharmacy (M.Pharm)

• B. Pharm/ M. Pharm from any reputed public/private University.

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

• Age At least 25 years

• 1 – 2 years of relevant experience in quality functions.

• Strong communication, collaboration skills

• Analytical Problem-solving and decision-making ability

• Integrity and continuous improvement mindset

• MS-Office and report preparation

• Ability to work under pressure and manage multiple operational requirements

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.

• Salary Negotiable, based on experience and qualifications

• Three Festival Bonuses yearly

• Contributory Provident Find

• Gratuity

• Profit Sharing (WPPF)

• Group Insurance

• Mobile Phone Allowance