Edwards Lifesciences seeks a Quality Engineer I to ensure compliance and optimize manufacturing processes for medical devices. The role involves investigating quality issues, implementing process improvements using engineering methods, and developing documentation to support production teams.

Responsibilities

- Investigate manufacturing quality and compliance issues; analyze results and develop corrective action reports
- Optimize manufacturing processes using Six Sigma and LEAN methodologies for continuous improvement
- Develop and maintain technical documentation, work instructions, and training materials for production teams
- Support risk management activities and maintain technical content of risk management files
- Train and coordinate technician activities; provide instruction on testing procedures and feedback

Requirements

- Bachelor's degree in Engineering or scientific field; Master's degree acceptable
- 5+ years of related quality or manufacturing engineering experience
- Fluent in Spanish and English
- Proficiency with MS Office Suite and CAD software
- Knowledge of statistical techniques and quality management systems
- Strong problem-solving, analytical, and critical thinking skills

📌 Quality Engineer I (España)
🏢 Edwards Lifesciences
📍 España