Production Compliance & Process Improvement Administrator

Al-Dawaa Medical Services Company; Saudi Arabia; Sur place; SAR 100 000 - 167 000; Plein temps

Résumé du poste

Al-Dawaa Medical Services Company in Saudi Arabia is seeking to administrate and control production documentation in line with ISO 13485 and SFDA requirements. The role focuses on optimizing resources, improving process efficiency, and ensuring full regulatory compliance.

You will manage Device History Records, BOM preparation for assembly lines, and maintain batch records and production logs while driving continuous improvement and operational excellence.

Qualifications

• Experience implementing ISO 13485 and SFDA requirements.
• Strong documentation and record-keeping capabilities.
• Ability to monitor KPIs and drive continuous improvement.

Responsabilités

• Administrate and control production documentation per regulatory requirements.
• Ensure Device History Records (DHR) for raw materials and batch records are complete.
• Plan daily activities on production lines and monitor performance against schedules.
• Identify process improvements to enhance productivity and reduce waste.
• Maintain safety, cleanliness, and proper working conditions on the production floor.

Connaissances

Regulatory compliance

Documentation

Quality control

Description du poste

Al-Dawaa Medical Services Company in Saudi Arabia is seeking to administrate and control production documentation in line with ISO 13485 and SFDA requirements. The role focuses on optimizing resources, improving process efficiency, and ensuring full regulatory compliance.

You will manage Device History Records, BOM preparation for assembly lines, and maintain batch records and production logs while driving continuous improvement and operational excellence.