Ziska Pharmaceuticals Limited is one of the fastest growing Pharmaceutical companies in Bangladesh. It is ISO 9001:2000 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 above position.

Job Responsibilities:

• Assist in formulation development, analytical method development, method validation, product optimization, and stability studies for various pharmaceutical dosage forms under the guidance of senior team members.
• Perform routine laboratory testing, raw material and finished product analysis, sample preparation, and maintain accurate records in accordance with GMP, GLP, and data integrity requirements.
• Prepare and maintain R&D documentation, including specifications, analytical methods, validation protocols, reports, product development records, and regulatory documents.
• Coordinate with Production, QA, QC, Engineering, Warehouse, Commercial, MSD, and Regulatory Affairs to support product development, technology transfer, process validation, and commercial manufacturing activities.
• Ensure proper use, cleanliness, calibration, and maintenance of laboratory equipment while complying with company SOPs, quality standards, safety regulations, and ISO 14001:2015 Environmental Management System (EMS) requirements.
• Perform any other duties assigned by the Department Head or Reporting Manager to support the objectives of the Research & Development Department.