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QA Specialist - Document Control
وصف الوظيفة
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.
المسؤوليات
- Establish and maintain a robust document management system for all quality assurance documentation
- Review and approve quality documents, including SOPs, change controls, and validation packages
- Coordinate the training and distribution of updated quality documents
- Monitor document changes and ensure proper version control, archiving, and retrieval
- Assist with internal and external audits related to document control processes
المؤهلات
- 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
- Proficient in Microsoft Office Suite