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 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.
Requirements
- 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.