Engineer II, Quality
Edwards Lifesciences · Wet, Costa Rica
QualityFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Edwards Lifesciences seeks a Quality Engineer II to ensure manufacturing compliance and optimize medical device production processes at a Costa Rica facility. The role involves investigating quality issues, managing regulatory documentation, and collaborating across teams to deliver cardiovascular products safely to patients.
What they're looking for
- Bachelor's degree in engineering or scientific field with 2+ years experience
- Master's degree in engineering or scientific field with industry or academic thesis/projects
- Experience working with laboratory or industrial equipment
- Proficiency with MS Office Suite; CAD skills preferred
- Understanding of statistical techniques and quality systems
- Strong analytical, problem-solving, and critical thinking abilities
- Excellent documentation, communication, and interpersonal skills
What you'll be doing
- Investigate manufacturing quality issues, complaints, and non-conformances; manage NCRs, CAPAs, and audit findings
- Review and disposition product holds; oversee material quality control and equipment validations
- Optimize manufacturing processes using Six Sigma, LEAN, and other engineering methods for continuous improvement
- Develop technical documentation, training materials, and risk management files for production teams
- Support process validation, quality metrics review, and material review boards
Privacy & handoff
This role links to Edwards Lifesciences's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.