Finished Goods QC Analyst – GMP/GLP Stability

Tamer Group Site; Jeddah; On-site; SAR 100,000 - 167,000; Full time

Job summary

SAJA plant is seeking a meticulous QC Analyst to join our quality team in Jeddah. You will perform analyses of stability studies, finished products, and raw materials in compliance with GMP and GLP standards, and prepare reports for management.

The role requires a Diploma in Pharmacy or a BSc in Science/Pharmacy, at least one year in related work, and strong attention to detail. Proficiency in MS Office and teamwork are essential.

Qualifications

• Diploma in Pharmacy or equivalent.
• 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.

Responsibilities

• Apply GMP and GLP regulations consistently.
• Analyze all Finished Product samples in accordance with the approved QCSM.
• Conduct regular daily and periodic analyses.
• Perform analysis of all raw materials based on 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.
• Record all analytical results in 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.

Skills

Teamwork

Attention to detail

Work under pressure

Microsoft Office

Education

Diploma in Pharmacy

Bachelor’s degree in Science or Pharmacy

Tools

Microsoft Office

Job description

SAJA plant is seeking a meticulous QC Analyst to join our quality team in Jeddah. You will perform analyses of stability studies, finished products, and raw materials in compliance with GMP and GLP standards, and prepare reports for management.

The role requires a Diploma in Pharmacy or a BSc in Science/Pharmacy, at least one year in related work, and strong attention to detail. Proficiency in MS Office and teamwork are essential.