QA Specialist - Document Control

About the role

EVA Pharma is seeking a meticulous QA Specialist focused on Document Control to join its Quality Assurance team at the factory in Hautat Sudair, Riyadh Province. The role ensures that all quality‑related documentation is managed, reviewed, and distributed in line with regulatory standards and internal policies.

Key responsibilities

• Establish and maintain a robust document management system for all QA records.
• Review, approve, and version‑control SOPs, change controls, validation packages, and other quality documents.
• Coordinate training and distribution of updated documents to relevant stakeholders.
• Monitor document changes, ensure proper archiving, and facilitate easy retrieval.
• Support internal and external audits by providing required documentation and maintaining audit readiness.

Required profile

• Bachelor’s degree in Life Sciences, Pharmacy, Quality Management or a related field.
• 1‑3 years of experience in quality assurance or document control within the pharmaceutical industry.
• Strong understanding of regulatory requirements such as cGMP and GDP.
• Excellent organizational abilities with high attention to detail.
• Effective communication skills and ability to work collaboratively across functions.

Required skills

• GDP
• cGMP
• Microsoft Office Suite
• Document management systems