Make a meaningful difference to patients around the world. Participate in quality systems processes, including applications, documentation, and training for the EEMEA region. Location: Valencia, Spain Duration: 6 months, 40 hours/week Start: Feb. 2025 How you will make an impact: Collaborating in QMS related topics for EEMEA region, e.g., Distributors management, CAPA, NCR, FCA, stop shipment. Participating in cross-functional teams for EEMEA quality system projects. Participating in quality system reports using dashboards and review for accuracy. Observing the impact of quality systems information and provide feedback to originators. What you will need: • Good computer skills in MS Office Suite. • Good written and verbal communication skills and interpersonal relationship skills. • Good problem-solving and critical thinking skills. • Good knowledge and understanding of Edwards policies, procedures, and guidelines relevant to quality systems. • Good knowledge of medical or pharmaceutical regulations as relating to documentation. • Basic understanding of medical devices regulations (e.g. ISO13485). • attention to detail. • Ability to interact effectively and professionally with all organizational levels and stakeholders. • Ability to manage competing priorities in a fast paced environment. • Must be able to work in a team environment, including immediate supervisor and other team members in a fast paced environment. Education and Experience: - University student of Biomedical Engineering, Biotechnology, or any other related field interested in medical device. - Fluent English required.