Specialist - QA

Ras Al Khaimah, United Arab Emirates

The position is responsible for ensuring manufacturing and packaging operations meet cGMP, SOP and product requirements through shop-floor quality oversight, accurate batch documentation and effective handling of quality issues.

• Perform line clearance and release activities, and timely in-process checks during manufacturing and packaging.
• Verify correct materials/components, gowning, cleanliness, environmental conditions and calibration of in-process equipment.
• Document and verify results; maintain traceable, accurate batch records, logbooks and labels. Review SOPs, batch manufacturing records (BMRs) and batch packaging records (BPRs).
• Investigate deviations and market complaints. Manage corrective and preventive actions (CAPA) and change control reports (CCR) in Ampelogic.
• Prepare Annual Product Quality Reviews (APQR); support audits and audit readiness, site gap assessments, GEMBA walks, sampling adherence follow-up and facility/process quality risk assessments.
• Follow environmental, health and safety requirements, use appropriate PPE and contribute to risk reduction and continual improvement.

3+ years in quality operations or manufacturing.

Bachelor’s degree in Pharmacy, Science or Chemical Engineering.

• GMP
• SOPs
• batch records
• Quality Management Systems (QMS)

Full Time

A pharmaceutical manufacturer based in Ras Al Khaimah producing generic medicines, diabetes care, consumer health and nutrition products. Its facilities supply markets across the Middle East, Africa and Asia, supported by production, quality, research and commercial teams.

Pharmaceutical

Quality Assurance

Not mentioned (apply as soon as possible)