Offer summary
Qualifications:
3-5 years' experience in medical device complaint handling, Strong knowledge of QSR and/or ISO 13485, Proven leadership experience preferred, Familiarity with Microsoft Office and TrackWise, Experience in medical device quality systems.
Key responsabilities:
- Lead and oversee complaint determination process
- Review inquiries to categorize them correctly
- Guide and train team on the process
- Identify and recommend process improvements
- Create and maintain documentation master files