Posted:1 day ago|
Platform:
Work from Office
Full Time
To lead, establish, maintain, and continually improve the Quality Management System (QMS) in accordance with ISO 13485:2016 and EUMDR.
Preparation and maintenance of Technical Files of Medical Equipment as per MDR 2017/745, ISO 14971, ISO 10993-1.
To plan, establish, document, implement, maintain, and update a post-market surveillance. He shall ensure that the post-market surveillance obligations comply with Article 10(10) of the EU Regulation 2017/745 & other applicable standards.
Design & development documentation.
Athena
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