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Senior Quality Engineer

stryker · Grecia

Nuevo
Senior 🇬🇧 English
21 CFR Part 820 ISO 13485 MDSAP FMEA statistical analysis quality risk management tools

Descripcion del puesto

About the role

We are looking for a Senior Quality Engineer to lead investigations of non‑conformances, implement corrective actions, and ensure our medical device products meet the highest quality standards.

Key responsibilities

  • Lead investigations of non‑conformances and drive corrective and preventive actions.
  • Collaborate with Engineering, Production and cross‑functional teams to meet quality requirements.
  • Support internal and external audits, prepare documentation and address observations.
  • Manage containment activities for non‑conforming product, including identification and segregation.
  • Monitor, analyze and trend quality data to identify risks and improvement opportunities.
  • Apply statistical analysis and risk management tools such as FMEA.

Required profile

  • Bachelor’s degree in Engineering or a related technical field.
  • Minimum 3 years of experience in Quality Engineering.
  • Working knowledge of 21 CFR Part 820, ISO 13485 and MDSAP.
  • Advanced English proficiency, written and verbal.

Required skills

  • 21 CFR Part 820 compliance
  • ISO 13485 compliance
  • MDSAP knowledge
  • Failure Mode and Effects Analysis (FMEA)
  • Statistical analysis
  • Quality risk management tools

Questions fréquentes

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Source : ats:workday

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