Healthcare
Document Controller Dammam, Saudi Arabia
Direct Employer / Verified Recruiter
Dammam
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HealthcareFull-time
Quality Manager open to all nationalities
Abdulghani Hussain Group
LocationAll KSA, KSA
SalaryNegotiable
Vacancies1 Open Role
Views43 views
Role at a Glance
Abdulghani Hussain Group has an opening for Quality Manager open to all nationalities in Saudi Arabia. This is a Full-time position in the Healthcare category. Salary is not disclosed in this posting, so confirm the full package with the employer before you accept. Apply directly by email using the buttons on this page. Khaleej Rozgar never charges candidates a fee. Posted on 10 Nov 2026 and valid until 10 Dec 2026.
Job Description & Details
Abdulghani Hussain Group is seeking a Quality Manager to lead quality assurance activities within its medical supplies or device manufacturing operations. The role involves ensuring compliance with regulatory standards and maintaining the quality management system. Responsibilities include: Registering medical products with the Saudi Food and Drug Authority (SFDA) and preparing MDMA files; Applying ISO 13485 requirements and managing the quality management system; Ensuring compliance with GMP and ISO 14971 risk management standards; Preparing and reviewing technical files, internal audits, verification and qualification procedures; Conducting CAPA, non‑conformity investigations and quality control activities; Communicating with regulators and preparing technical documentation in English. The position is open to all nationalities, with immediate recruitment and a remunerative salary to be determined after a personal interview.
Candidate Requirements
- ✓Bachelor of Biomedical Engineering
- ✓Industrial Engineering
- ✓Pharmacy or a related discipline
- ✓At least two years of experience in quality
- ✓preferably in medical supplies or device factories
- ✓Practical experience in quality within medical factories
- ✓Experience registering medical products with the Saudi Food and Drug Authority (SFDA) and preparing MDMA files
- ✓Good knowledge of ISO 13485 requirements and quality management system application
- ✓Familiarity with GMP requirements and ISO 14971 risk management standards
- ✓Experience preparing and reviewing technical files
- ✓internal audit
- ✓verification and qualification procedures
- ✓Experience in CAPA
- ✓non‑conformity investigation and quality control
- ✓Proficiency in English
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