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.