Overview

In this role you will apply quality engineering principles to ensure regulatory compliance and to optimize product development, manufacturing, and distribution. You will partner with cross-functional teams to influence decisions across the product lifecycle, driving continuous improvement and rigorous risk management. You’ll investigate quality and compliance issues, implement CAPA, and support training and documentation to enable smooth project handoffs. This position offers the chance to impact patients worldwide by enabling safe, high-quality medical technologies.

Responsabilidades

- Apply quality engineering methods to ensure regulatory and company compliance across development, manufacturing, and distribution
- Investigate quality and compliance issues (CAPA, non-conformances, audit observations) and develop data-driven recommendations
- Optimize manufacturing processes using Six Sigma and Lean for design-for-manufacturing and ongoing improvements




- Identify opportunities to redesign equipment, tools, or fixtures to reduce risk and improve processes
- Develop/update risk management documentation and produce production training and work instructions
- Assign tasks, guide technicians on testing, provide feedback, and coordinate team activities
- Perform other duties as assigned by leadership

Requisitos principales

- Bachelor's Degree in Engineering or scientific field OR Master's Degree or equivalent
- 5 years of related work experience
- Fluent in Spanish & English

- Documentation and interpersonal communication
- Problem-solving, analytical, and critical thinking
- Ability to interact professionally with all organizational levels
- MS Office Suite
- CAD experience
- statistical techniques

📌 Quality Engineer I - Edwards Lifesciences (Valencia)
🏢 Edwards Lifesciences
📍 Valencia