PpbMTIC InterCert /b of bMTIC Group /b is growing steadily and successfully in all areas of Certification, particularly as a Notified Body (CE 0068) in bMedical Device Certification. /b /p pTechnical Experts, Lead Auditors Auditors for Conformity Assessment activities for Medical Devices according to EU Regulation 2017/745 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 13485 audits. /p pbThis opportunity is only available to candidates residing in Italy. /b /p pWe are currently looking for the following additional specific requirements: /p h3Auditor /h3 ul liUniversity degree in engineering discipline or chemical science or pharmacy /li liMinimum 4 years of Work experience in medical manufacturer. /li liSound knowledge of Regulation (EU) 2017/745 and MDD 93/42/EEC /li liSound knowledge of the main horizontal harmonized standards including, but not limited to ISO 13485, ISO 14971 /li liKnowledge of English language /li liLead Auditor training course according to ISO 19011 (40 hours) will be a plus /li /ul h3Product Reviewer/Final reviewer /h3 ul liUniversity degree in engineering discipline or chemical science or pharmacy /li liMinimum 4 years of Work experience in medical manufacturer of which at least 2 years in quality management or as auditor for other notified bodies. /li liSound knowledge of Regulation (EU) 2017/745 and MDD 93/42/EEC /li liSound knowledge of the main horizontal harmonized standards including, but not limited to ISO 14971, ISO 10993series, EN 62366 /li /ul /p #J-18808-Ljbffr