QA Administration & Document Review Specialist

EVA Pharma

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.

Key Responsibilities:

• Review and approve Quality Assurance documents, including SOPs, specifications, and validation protocols, ensuring compliance with regulatory standards.
• Maintain an organized document control system to manage the lifecycle of quality documents from creation to archiving.
• Support ongoing training initiatives by ensuring that relevant documentation is accessible and up to date.
• Coordinate internal audits for documentation practices and assist in preparation for external audits.
• Collaborate with cross-functional teams to address any documentation-related issues and promote a culture of quality.

• Bachelor s degree is a must.
• 0-2 years of experience in quality assurance, document control, or regulatory compliance within the pharmaceutical industry.
• Problem Solving and Analytical Thinking.
• Excellent attention to detail and organizational skills, with the ability to manage multiple priorities and meet deadlines.
• Effective communication and interpersonal skills to work collaboratively with various teams.
• Proficient in Microsoft Office Suite and familiar with quality management software.