Ingeniero de Calidad I - Crecimiento B2B Industrial

Martinezyasociados; Valencia; On-site; EUR 45,000 - 65,000; Full time

Job summary

Edwards Lifesciences, Valencia site, seeks a Quality Engineer I to support regulatory-compliant product development and manufacturing. You will work with cross-functional teams to address CAPA, audits, and improvements using Six Sigma and LEAN techniques.

The role requires a engineering degree, 5 years in quality roles, and fluency in Spanish and English, with strong documentation and collaboration skills to advance patient safety and product quality.

Qualifications

• Bachelor's or Master's degree in Engineering or a scientific field.
• Minimum 5 years related work experience.
• Fluent in Spanish and English.
• Strong documentation and interpersonal skills.

Responsibilities

• Apply quality engineering principles to ensure regulatory compliance and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution.
• Investigate manufacturing quality and compliance issues (CAPA, non-conformances, audit observations) for all production processes prior to final product release; analyze results and develop reports.
• Use Six Sigma and LEAN methods to optimize manufacturing processes and identify redesign opportunities to reduce risk.
• Develop, update, and maintain risk management files as needed.
• Create training and production documentation to enable knowledge transfer of project and manufacturing processes.
• Assign tasks, supervise technicians, and coordinate testing activities.
• Other duties as assigned by Leadership.

Skills

Quality engineering

Regulatory compliance

CAPA

Problem solving

Spanish language

English language

Six Sigma

Lean methods

Statistical techniques

Lab/industrial equipment knowledge

Education

Bachelor's degree in engineering

Master's degree in engineering

Tools

MS Office

CAD

Power BI

Power Automate

Job description

Edwards Lifesciences, Valencia site, seeks a Quality Engineer I to support regulatory-compliant product development and manufacturing. You will work with cross-functional teams to address CAPA, audits, and improvements using Six Sigma and LEAN techniques.

The role requires a engineering degree, 5 years in quality roles, and fluency in Spanish and English, with strong documentation and collaboration skills to advance patient safety and product quality.