Y-LOGIMED S.M.S.A. member of the Hellenic Healthcare Group is seeking for immediate hiring:

Quality and Regulatory Affairs Coordinator

Based in Y-Logimed’s Branch in Thermi/ Thessaloniki

Fixed-term contract: 6 months.

Summary:

The Quality and Regulatory Affairs Coordinator will work with our Quality and Regulatory Team to support Y-Logimed’s Regulatory Project, following standardized procedures and processes.

Responsibilities:

• Document Management of Medical Devices Regulatory Documentation according to the MDR 2017/745 through the Company’s CRM System.
• Registration of Medical Devices in the Greek Competent Authorities and communication with the Authorities to successfully implement all necessary registration procedures.
• Support collection of all necessary documentation through a standardized process.
• Support to the Quality and Regulatory Affairs Teams daily workflow.

Qualifications:

• An undergraduate degree, BS or BA is required.
• Very good knowledge in MS Excel and Microsoft software programs is required.
• Knowledge of CRM Program will be considered a plus.
• Previous professional experience in the field of Quality and Regulatory Affairs will be considered a plus.
• Dedication to the project’s targets and to agreed timetable of deliverables.
• Effective collaboration with the Quality and Regulatory Affairs Team and other Company’s Units.

Please submit your resume through our website https://www.y-logimed.gr.

For any inquiries, you may contact our HR department at +30 210 2802077.