Regulatory Affairs Specialist Uri

Regulatory Affairs Specialist
Uri
Sardegna, Uri

MECTRON SPA , A DESIGNER AND MANUFACTURER OF DENTAL AND MEDICAL DEVICES IS LOOKING FORRegulatory Affairs Specialist The Regulatory Affairs Specialist assists the SeniorRegulatory Affairs Managerin the registration of medical devices in EXTRA-CEE countries following a plan that is constantly updated in accordance with company strategy.

Essential Duties andResponsibilities prepares, updatesand reviews the documents for use in in regulatory dossiers in accordance with EU MOR 745/2017 and international requirements.

Prepares and manages technicaldocumentations needed for submission and registrations; Interacts with project developments teams in order to collect the information needed for submissions/ registrations and advise them on matters that are related to regulatory processes and compliance Registers, monitors, and maintains registrations for the company's medical devices with EXTRA - CEE countries' competent authorities as appropriate; Assist in theCompliance to the Medical Device Regulations (MDR) in the EU, Canadian Medical Device Directive, FDA, TGA, ANVISA, Japan Authority and other regulatory agencies; Is also proficient in applicable standards and regulations including: ISO 13485, ISO 9001, ISO 14971, ISO 10993, ISO 11607 and MEDDEV guidelines; Prepares and updates the Quality and Regulatory Agreements necessary for registration purposes, distribution contracts and technical assistance for the EXTRA - CEE countries concerned; Follows and promotes corporate quality procedures and standards in order to achieveand maintain adequate results; Actively participate in audit activities. Work Experience - Required Qualifications • At least 3 years' experience with Regulatory Affairs in the medical device industry preferred; • ISO 13485 • Fluent in English; • Internal Auditor Qualifications preferred. Educational Requirements Bachelor's Degree in scientific discipline; Higher-level education degree preferred.