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.