**MTIC InterCert** is growing steadily and successfully in all areas of Certification, particularly as a **Notified Body** in **Medical Device Certification**. Technical Experts, Lead Auditors, Auditors and Clinical specialists for Conformity Assessment activities for Medical Devices according to Directive 93/42/EC and soon, for EU Regulation 2017/745 are always welcome to cooperate with our team at our offices in Europe: activities will include both technical documentation assessments and QMS audits, including EN ISO 13485 audits. 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 of which at least 2 years in quality management or as auditor for other notified bodies.
- Sound knowledge of MDD 93/42/EEC and Regulation (EU)



2017/745
- Sound knowledge of the main horizontal harmonized standards including, but not limited to ISO 13485, ISO 14971
- Knowledge of English language
- Lead Auditor training course according to ISO 19011 (40 hours) will be a plus **Product Reviewer/Final reviewer**:
General Requirements: - University degree in engineering discipline or chemical science or pharmacy
- Sound knowledge of Regulation (EU) 2017/745
- Sound knowledge of the main horizontal harmonized standards including, but not limited to ISO 14971, ISO 10993series, EN 62366
- Knowledge of English language Contratto di lavoro: Tempo completo Disponibilità: - Dal lunedì al venerdì Sede di lavoro: Di persona

📌 Medical Devices Auditors / Product Reviewer (Rho)
🏢 MTIC GROUP
📍 Rho