Senior Qa/ra Specialist

ResMed

Multiple Locations
Iso 13485 knowledge
Medical device regulation expertise
Quality management system maintenance
The primary role is to ensure compliance with regulatory frameworks and quality requirements

Job Summary

  • The primary role is to ensure compliance with regulatory frameworks and quality requirements.
  • You will support and maintain an acquired company on all QMS and Regulatory aspects.
  • ResMed offers a diverse and inclusive culture that encourages individual expression and innovative ideas.

Matching Summary

The primary role is to ensure compliance with regulatory frameworks and quality requirements.

Skills & Requirements

Must-have

  • ISO 13485 knowledge
  • Medical Device Regulation expertise
  • Quality Management System maintenance

Nice-to-have

  • Experience in software companies
  • Strong communication skills
  • Proactive and self-starter

Key Requirements

  • Bachelor's degree in technical field
  • At least one year in regulatory affairs
  • Four to five years of related experience

Work Rights

Not specified

Tailored Resume

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