Senior Quality Assurance Engineer

Stryker

Cork, Ireland
Hybrid
2+ years in medical device industry
Experience in post-market surveillance
Knowledge of iso 9001 or iso 13485
Ensure timely closure of complaints records to comply with FDA requirements

Job Summary

  • Ensure timely closure of complaints records to comply with FDA requirements.
  • Participate and lead in continuous improvement and process re-engineering projects.
  • Provide support to the new product development and risk management process.

Matching Summary

Ensure timely closure of complaints records to comply with FDA requirements.

Skills & Requirements

Must-have

  • 2+ years in Medical Device Industry
  • Experience in Post-Market Surveillance
  • Knowledge of ISO 9001 or ISO 13485

Nice-to-have

  • Mentoring team members
  • Continuous improvement initiatives
  • Cross-functional collaboration

Key Requirements

  • Level 8 Degree in Engineering
  • Demonstrated applied knowledge of regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter