Quality Engineer I — Shape Life-Saving Medical Tech

Cronoshare.Com; Valencia; On-site; EUR 60,000 - 100,000; Full time

Job summary

Edwards Lifesciences in Valencia, Spain, is seeking a Quality Engineer I to help ensure regulatory compliance and optimize product development across the lifecycle. The role focuses on quality systems, CAPA handling, and process improvements in a fast-paced manufacturing environment.

The candidate will apply Six Sigma and LEAN methods, contribute to risk management files, and develop training materials for production teams, while collaborating with multiple departments to deliver high-integrity

Qualifications

• Bachelor's degree or higher in engineering or scientific field.
• 5 years of related work experience.
• Fluent in Spanish and English.

Responsibilities

• Applies quality engineering principles to ensure regulatory compliance and optimize product development and manufacturing processes.
• Investigate manufacturing quality and compliance issues (CAPA, non-conformances, audits) for production before final release.
• Use Six Sigma and LEAN methods to improve design for manufacturing and process efficiency.
• Develop, update, and maintain risk management documentation.
• Create training materials and work instructions to facilitate knowledge transfer.

Skills

Quality engineering principles

Six Sigma

Lean methodologies

Statistical techniques

MS Office Suite

CAD experience

Problem solving

Communication skills

Team collaboration

Analytical thinking

Education

Bachelor's Degree in Engineering or scientific field

Master's Degree or equivalent in Engineering or scientific field

Tools

Power BI

Power Automate

Job description

Edwards Lifesciences in Valencia, Spain, is seeking a Quality Engineer I to help ensure regulatory compliance and optimize product development across the lifecycle. The role focuses on quality systems, CAPA handling, and process improvements in a fast-paced manufacturing environment.

The candidate will apply Six Sigma and LEAN methods, contribute to risk management files, and develop training materials for production teams, while collaborating with multiple departments to deliver high-integrity