14 Sep
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Anonymous
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Ranchi
4 years) 10 years) of professional experience as an auditor and/or product assessor at a Notified Body for the MDR Regulation (EU) 2017/745. Your professional experience demonstrates a wide range of medical devices (MDA and/or MDN codes) and technologies (MDT codes). In-depth knowledge of MDR, ISO 13485, MDSAP documents, as well as other regulatory requirements, MDCG guidelines and product standards. Recognized and proven qualifications as Lead Auditor for MDR, ISO 13485 and ideally MDSAP. Strong ability to assess complex technical and clinical issues. High degree of personal responsibility, objectivity and skilled communication. Willingness to travel internationally (as required) MDR Code Requirement: MDN 1102/A - Non-active osteo- and orthopaedic implants - Rigid MDN 1102/B - Non-active osteo- and orthopaedic implants - Joint MDS 1003 - Devices manufactured utilising tissues or cells of animal origin, or their derivatives
📌 Lead Auditor For Medical Devices (Ranchi)
🏢 Anonymous
📍 Ranchi