RM, Analyst

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.

• 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.

• 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

• Arabic: Mandatory
• English: Important