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.