Officer- Quality Control (Compliance & Validation)

Job Description

Title: Officer- Quality Control (Compliance & Validation)

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)
• Bachelor of Science (BSc) in Chemistry, Biochemistry
• Master of Science (MSc) in Chemistry, Biochemistry

• B. Pharm/ M. Pharm/B. Sc/ M. Sc in Chemistry/Biochemistry 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 IPQC & Documentation and Validation

• 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 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.

• Salary Negotiable, based on experience and qualifications

• Three Festival Bonuses yearly

• Contributory Provident Find

• Gratuity

• Profit Sharing (WPPF)

• Group Insurance

• Mobile Phone Allowance