RM, Analyst

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

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

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.