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Job Description
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.
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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.
Skills
European Union Medical Device RegulationQaRegulatory AffairsRARegulatoryDevicesMedical DevicesEuropeanMaintenanceIf a job posting appears fraudulent, asks for payment, contains misleading information, or violates our guidelines, please report it immediately. Our team will review it promptly, Jobaaj does not charge any fee from the applicants.
Important dates & deadlines?
Application Deadline
20 Nov 25, 12:57 PM IST
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