OverviewIn 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.
ResponsabilidadesApply 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 principalesBachelor'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 (España)
🏢 Edwards Lifesciences
📍 España