Your responsibilities will include:
- Maintenance and optimisation of the Quality Management System.
- Managing technical change requests and Non-Conformities.
- Participation in audits, arranging of supplier audit processes.
- 4+ years of experience in Quality Management for medical devices.
- Strong knowledge of ISO 13485.
- Experience with supplier quality is desirable.
- Flat hierarchy, very collaborative culture.
Please contact Hollie Barry for further information on this position and/or others in the medical device industry: firstname.lastname@example.org