MTIC InterCert of MTIC Group is steadily and solidly growing in all areas of Certification, particularly as a Notified Body (CE 0068) for Medical Device Certification.

Due to staff expansion and the opening of a new office in Emilia-Romagna, we are looking for Technical Experts, Lead Auditors, and Auditors for Medical Device Conformity Assessment activities in accordance with Regulation (EU) 2017/745. Activities will include both technical documentation assessments and Quality Management System (QMS) audits, including audits according to EN ISO 13485.

This opportunity is exclusively available to candidates residing in Italy.

Work location: Rho / Emilia-Romagna

We are currently looking for the following additional specific requirements:

Product Reviewer / Final Reviewer

• University degree in engineering, chemical sciences, or pharmacy
• Minimum 4 years of work experience with a medical device manufacturer, of which at least 2 ...