Spécialiste Systèmes Qualité
Medtronic(1 day ago)
About this role
This role involves developing, maintaining, and supporting the Quality Management System programs in compliance with ISO 13485, FDA, and local regulatory requirements. The position allows for engagement in quality investigations, audits, data analysis, and continuous improvement initiatives within a leading medical devices company.
Required Skills
- Quality Management
- ISO 13485
- Regulatory Compliance
- Audit
- CAPA
- Data Analysis
- Documentation
- Process Improvement
- Quality Assurance
- Medical Devices
Qualifications
- Master's Degree in Quality
About Medtronic
medtronic.comPeople-centered, data-driven, personalized. Solving our world’s biggest health challenges with advanced technology.
View more jobs at Medtronic →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Medtronic
Similar Jobs
Senior Quality Engineer (San Diego, CA)
Synchron(1 month ago)
Quality Systems Engineer
Re:Build Manufacturing(1 month ago)
Staff Quality Engineer (Manufacturing Site, Grecia)
Stryker(1 month ago)
Quality Assurance Manager
Carrier(29 days ago)
Quality System Auditor
Kimball Electronics(1 month ago)
Manufacturing Engineer 1
Jabil(28 days ago)