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 seeking a detail-oriented and organized QA Administration & Document Review Specialist to join our dynamic Quality Assurance team.The ideal candidate will ensure that the documentation and records adhere to regulatory standards, while contributing to the overall quality management system.Key Responsibilities:Review and approve Quality Assurance documents, including SOPs, specifications, and validation protocols, ensuring compliance with regulatory standardsMaintain an organized document control system to manage the lifecycle of quality documents from creation to archivingSupport ongoing training initiatives by ensuring that relevant documentation is accessible and up to dateCoordinate internal audits for documentation practices and assist in preparation for external auditsCollaborate with cross-functional teams to address any documentation-related issues and promote a culture of qualityRequirementsBachelor's degree is a must0-2 years of experience in quality assurance, document control, or regulatory compliance within the pharmaceutical industryProblem Solving and Analytical ThinkingExcellent attention to detail and organizational skills, with the ability to manage multiple priorities and meet deadlinesEffective communication and interpersonal skills to work collaboratively with various teamsProficient in Microsoft Office Suite and familiar with quality management software