About this role
Position: QC Analyst Location: Jeddah, Plant Job Summary: Responsible for the analysis of all SAJA Stability Studies, Finished Products, and Raw Materials received at the SAJA plant, in compliance with GMP and GLP standards. Objectives:
• Apply all GMP and GLP regulations consistently. • Analyze all SAJA Finished Product samples in accordance with the approved QCSM. • Conduct regular daily and periodic analyses. • Perform analysis of all raw materials received at SAJA, based on the latest pharmacopeial monographs and GLP guidelines. • Carry out stability study analyses for all products. • Prepare comprehensive reports based on analytical results. • Submit analysis and test reports to the direct manager. • Accurately record all analytical results in compliance with the QC system. • Record and monitor the conditions of stability chambers. • Calibrate balances and pH meters. • Manage and reserve retained samples. • Control and monitor the inventory of chemicals and solvents. • Perform other duties as assigned by the direct supervisor or manager. Requirement :
• Diploma in Pharmacy • Bachelor’s degree in Science or Pharmacy • Minimum of one year in a related field • Team-oriented with strong collaboration skills • Ability to work under pressure • High level of accuracy and attention to detail • Proficient in Microsoft Office and related computer applications Languages :-
• Arabic: Mandatory • English: Important