Quality & Regulatory Affairs_nl

Quality & Regulatory Affairs


Quality & Regulatory Affairs

Quality

The Quality department of Terumo Europe, operating form our HQ in Belgium, provides support related to Quality Systems (QS), Quality Assurance (QA) and Quality Control (QC). The team provides its support towards internal and external customers. We contribute directly to Terumo Europe being a core player in the EMEA Healthcare market, providing best in class quality products and services, meeting customer and regulatory requirements, supported by an effective Quality Management System. We count on each and everyone of our team to contribute to the quality of our products and services to achieve this vision.

Quality

The Quality department of Terumo Europe, operating form our HQ in Belgium, provides support related to Quality Systems (QS), Quality Assurance (QA) and Quality Control (QC). The team provides its support towards internal and external customers. We contribute directly to Terumo Europe being a core player in the EMEA Healthcare market, providing best in class quality products and services, meeting customer and regulatory requirements, supported by an effective Quality Management System. We count on each and everyone of our team to contribute to the quality of our products and services to achieve this vision.

Regulatory Affairs & Vigilance

Regulatory Affairs is assuring in a demanding and continuously evolving regulatory environment as well as a changing business environment that the medical devices of Terumo are safe and effective and are made accessible to users and patients in the shortest possible time.

The Complaint & Vigilance department is assuring the post market surveillance for medical devices manufactured and/or sold by Terumo Europe N.V. by an established complaint handling process, by timely performing vigilance reporting and by executing product recalls whenever deemed necessary.

Regulatory Affairs & Vigilance

Regulatory Affairs is assuring in a demanding and continuously evolving regulatory environment as well as a changing business environment that the medical devices of Terumo are safe and effective and are made accessible to users and patients in the shortest possible time.

The Complaint & Vigilance department is assuring the post market surveillance for medical devices manufactured and/or sold by Terumo Europe N.V. by an established complaint handling process, by timely performing vigilance reporting and by executing product recalls whenever deemed necessary.

 

Interested in using your expertise to help our business grow in a compliant way? Check out our current open vacancies!

 

Interested in using your expertise to help our business grow in a compliant way? Check out our current open vacancies!

Zoekresultaten voor "". Pagina 1 van 1, resultaten 1 t/m 3 van 3
Titel Plaats Datum Sort descending Afdeling
RA / QA Specialist
RA / QA Specialist Nederland 17 jul. 2024
Nederland 17 jul. 2024 Quality & Regulatory Affaire
QC Lab Technician
QC Lab Technician België 13 jul. 2024
België 13 jul. 2024 Quality & Regulatory Affaire
Senior QA&RA officer
Senior QA&RA officer Nederland 25 jun. 2024
Nederland 25 jun. 2024 Quality & Regulatory Affaire

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