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3 days ago
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Full time
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six sigma doe iso 13485 capa pfmea

📋 Description

  • Ensure that manufacturing processes comply with quality standards.
  • Perform follow-ups and monitor Quality Notifications (VR's, NCR's, EE's).
  • Support corrective and preventive actions (CAPAS).
  • Prepare trend reports and analyze major offenders.
  • Participate in process and product validations.
  • Conduct improvement projects for defect reduction.

🎯 Requirements

  • Bachelor's Degree in any engineering field
  • Advanced English
  • 5 years experience as Quality Engineer or Manufacturing Engineer
  • 5 years experience in process validations
  • 3 years experience in quality audits for medical products
  • 3 years experience in the medical industry
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