Navana Pharmaceuticals PLC

Responsibilities & Context Conduct quality analysis of raw materials, packaging materials, bulk products, and finished pharmaceutical products. Perform testing and analysis for ongoing stability studies of finished pharmaceutical products. Operate and maintain QC analytical instruments such as IR spectroscopy, UV-Vis spectroscopy, HPLC, GC, and other chromatographic equipment. Prepare, update, and maintain laboratory documentation in accordance with cGMP requirements. Follow laboratory SOPs, GLP, GMP, safety procedures, and applicable quality standards. Ensure accurate recording, reporting, and documentation of analytical test results. Perform other quality control and laboratory-related duties assigned by management to support departmental and organizational objectives.