MTIC GROUP
Medical Devices Auditors / Product Reviewer
Job Location
Rho, Italy
Job Description
About the job MTIC InterCert is experiencing steady growth in all areas of Certification, particularly as a Notified Body in Medical Device Certification. We are seeking Technical Experts, Lead Auditors, Auditors, and Clinical Specialists for Conformity Assessment activities related to Medical Devices according to Directive 93/42/EEC and EU Regulation 2017/745. These roles involve technical documentation assessments and QMS audits, including EN ISO 13485 audits. We are currently looking for candidates with the following specific requirements: Auditor University degree in engineering, chemical science, or pharmacy Minimum 4 years of work experience in medical manufacturing, including at least 2 years in quality management or as an auditor for other notified bodies Sound knowledge of MDD 93/42/EEC and Regulation (EU) 2017/745 Knowledge of main horizontal harmonized standards such as ISO 13485 and ISO 14971 Proficiency in English Lead Auditor training course according to ISO 19011 (40 hours) is a plus General Requirements: University degree in engineering, chemical science, or pharmacy Knowledge of Regulation (EU) 2017/745 Knowledge of main horizontal standards such as ISO 14971, ISO 10993 series, EN 62366 Proficiency in English Ability to commute / relocate: Reliably commute or plan to relocate to 20017 Rho, LOM before starting work Work Location: One location J-18808-Ljbffr
Location: Rho, Lombardia, IT
Posted Date: 7/25/2025
Location: Rho, Lombardia, IT
Posted Date: 7/25/2025
Contact Information
Contact | Human Resources MTIC GROUP |
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