MTIC InterCert
of
MTIC Group
is growing steadily and successfully in all areas of Certification, particularly as a Notified Body (CE ****) in
Medical Device Certification.
Technical Experts, Lead Auditors & Auditors for Conformity Assessment activities for Medical Devices according to EU Regulation ****?745 are always welcome to cooperate with our team at our offices in Rho, Milan, Italy: activities will include both technical documentation assessments and QMS audits, including EN ISO ***** audits.
This opportunity is only available to candidates residing in Italy.
We are currently looking for the following additional specific requirements:
Auditor:
University degree in engineering discipline or chemical science or pharmacy
Minimum 4 years of Work experience in medical manufacturer.
Sound knowledge of Regulation (EU) ****?745 and MDD *****/EEC




Sound knowledge of the main horizontal harmonized standards including, but not limited to ISO *****, ISO *****
Knowledge of English language
Lead Auditor training course according to ISO ***** (40 hours) will be a plus
Product Reviewer/Final reviewer:
University degree in engineering discipline or chemical science or pharmacy
Minimum 4 years of Work experience in medical manufacturer of which at least 2 years in quality management or as auditor for other notified bodies.
Sound knowledge of Regulation (EU) ****?745 and MDD *****/EEC
Sound knowledge of the main horizontal harmonized standards including, but not limited to ISO *****, ISO *****series, EN *****
Knowledge of English language

📌 Medical Devices Auditors & Product Reviewer (Milano)
🏢 MTIC GROUP
📍 Milano