**About the job**
**MTIC InterCert **with its over 50 years of experience and knowledge in the field of testing, inspection, certification and testing has been serving to its customers internationally.
MTIC InterCert is growing steadily and successfully in all areas of Certification, particularly as a Notified Body in Medical Device Certification. Currently we are recruiting Technical Coordinator for Conformity Assessment activities for Medical Devices according to EU Regulation 2017/745 to join our Team in **Rho, Milano.**
**Your responsibilities**:
- Support Medical Devices Certification Office to coordinate inspectors and various stakeholders (auditors, customers...) according to various requests.
- Collaborate with the Competence Centers in the various countries of the world: maintain relations with reference colleagues in the destination countries, to manage the files and solve the related anomalies.
- Support the Medical Devices Technical Department to contact clients and prepare quotations.
- Collaborate with other business functions involved to ensure the certification path;
- Coordinate the personnel in compliance with the rules and requirements defined by both control bodies (National and international accreditation and standardization bodies) and relevant certification schemes/standards.
**Key Requirements**:
- Diploma or Degree in Biomedical Engineering or equivalent.
- Basic knowledge of MDD 93/42/EEC and Regulation (EU) 2017/745
- Basic knowledge of the main horizontal harmonized standards including, but not limited to ISO 13485, ISO 14971
- Proactive team player with the ability to work independently in challenging projects and timelines
- Knowledge of English
- Strong written and oral communication skills
Contratto di lavoro: Tempo indeterminato
Disponibilità:
- Dal lunedì al venerdì
Domande di preselezione:
- How many years of experience do you have in the field of Medical devices Certification
Lingua:
- Inglese (Obbligatorio)
Sede di lavoro: Di persona