Join EVA Pharma, a leading pharmaceutical company committed to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are dedicated to fostering a supportive and innovative environment for our team members.

We are looking for a meticulous and dedicated QA Specialist - Document Control to join our Quality Assurance team at EVA Pharma's factory in Hautat Sudair, Riyadh Province, Saudi Arabia..

The ideal candidate will play a crucial role in ensuring that all quality-related documents are managed effectively, adhering to regulatory requirements and best practices.

Key Responsibilities:

• Establish and maintain a robust document management system for all quality assurance documentation, ensuring compliance with applicable regulations and internal standards.
• Review and approve quality documents, including SOPs, change controls, and validation packages, ensuring accuracy and completeness.
• Coordinate the training and distribution of updated quality documents to relevant stakeholders within the organization.
• Monitor document changes and ensure proper version control, archiving, and retrieval of documents as needed.
• Assist with internal and external audits related to document control processes and maintain audit readiness.

Requirements

• Bachelor's degree in a related field such as Life Sciences, Pharmacy, or Quality Management.
• 1-3 years of experience in quality assurance or document control within the pharmaceutical or related industry.
• Strong understanding of regulatory requirements (cGMP, GDP, etc.) and quality management principles.
• Excellent organizational skills with high attention to detail and accuracy.
• Strong communication skills and ability to work collaboratively with cross-functional teams.
• Proficient in Microsoft Office Suite; experience with document management systems is a plus.