Quality Assurance Specialist - Documentation

About the role

This full-time, on-site position is based in 10th of Ramadan and focuses on maintaining accurate, up-to-date quality assurance documentation. The specialist will ensure all records comply with GMP, GDP and the company’s Quality Management System while supporting audits and continuous improvement.

Key responsibilities

• Prepare, review, issue, and maintain controlled quality documents such as SOPs, work instructions, forms, and specifications.
• Manage document version control, periodic reviews, archival activities and change-control updates.
• Maintain document control logs and ensure all quality records are accurate and current.
• Support internal, customer and regulatory audits by providing required documentation.
• Coordinate training documentation for newly issued or revised procedures.
• Collaborate with cross-functional teams to guarantee documentation accuracy and regulatory compliance.
• Participate in continuous-improvement initiatives related to document control and quality systems.

Required profile

• Bachelor’s degree in quality management, science or a related field (preferred).
• 2–4 years of experience in Quality Assurance, preferably in documentation control or regulated industries such as pharmaceuticals, manufacturing or FMCG.
• Strong knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Excellent attention to detail, organizational and communication skills.

Required skills

• Proficiency in Microsoft Office.
• Experience with document management systems.