Master in Quality Assurance Specialist

Gruppo MIDI S.r.l. is seeking highly motivated and qualified professionals to join our team as Master in Quality Assurance for Medical Devices and IVD. This is a unique opportunity to develop your skills and knowledge in quality assurance, regulatory affairs, and auditing.

The Master in Quality Assurance for Medical Devices and IVD is a 112-hour online program designed to equip professionals with the necessary skills and knowledge to work in the medical device industry. The program covers topics such as quality management systems, regulatory affairs, auditing, and quality assurance.

• Quality management systems and auditing
• Regulatory affairs and compliance
• Quality assurance and control
• Medical device development and manufacturing

• 4 certifications: Auditor/Lead Auditor of Quality Management Systems, Quality Assurance Regulatory Affairs Expert, ISO 13485 Auditor and Lead Auditor, and Quality Assurance and Regulatory Affairs Professional
• 112 hours of online training
• Access to a community of professionals in the medical device industry

This program is designed for professionals who want to develop their skills and knowledge in quality assurance, regulatory affairs, and auditing. The ideal candidate has a degree in a scientific or engineering field or a diploma in chemistry or biology.

To apply, please submit your application and consent to the processing of your personal data. The program is open to candidates of all ages and nationalities.