Quality Control Analyst – Finished Product/Stability

About the role

The Quality Control Analyst – Finished Product/Stability will perform in‑process, finished‑product and stability testing of pharmaceutical products at our Al‑Qastal Industrial Area facility in Amman. Working under GMP and GLP guidelines, the analyst ensures product quality, safety and regulatory compliance through accurate testing, data recording and sample management.

Key responsibilities

• Conduct in‑process, finished‑product and stability tests following approved methods and SOPs.
• Execute and monitor stability studies, manage sample storage conditions and schedule withdrawals.
• Record, analyze and document test results in compliance with GMP, GLP and data‑integrity principles.
• Investigate deviations or out‑of‑specification results together with cross‑functional teams.
• Participate in method validation, transfer activities and SOP updates.
• Mentor and train junior staff on testing techniques and compliance requirements.
• Communicate study findings and progress to supervisors and relevant departments.

Required profile

• Bachelor’s degree in Chemical Engineering or related field.
• Minimum 1 year of Quality Control experience in pharmaceutical manufacturing.
• Strong command of written and spoken English.
• Good understanding of GMP, GLP and data‑integrity principles.
• Excellent analytical, documentation, communication, teamwork and time‑management abilities.

Required skills

• GMP
• GLP
• Data Integrity