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
