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Posted · 16.09.2026
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# Medical Device Site Auditors / Product Reviewers

Notice - Notified Body 2764

At Notice we are recruiting for Medical Device Site Auditors, Active Medical Device Product Reviewers & Non-Active Medical Device Product Reviewers (EU MDR). We are particularly interested in experts authorized or eligible for authorization under the following codes : For Site Auditors- MDT Codes: MDT 2001, MDT 2003, MDT 2004, MDT 2005, MDT 2007, MDT 2009, MDT 2010, MDT 2012, MDT 2013 For Active Product Reviewers- MDA Codes: MDA 0302, MDA 0204, MDA 0302, MDA 0306, MDA 0307, MDA 0308, MDA 0312 (esp. ventilators, infusion pumps, surgical lasers, retinal cameras, electrosurgical instruments, BP monitors, spirometers) For Non- Active Product Reviewers- MDN Codes: MDN 1101 , MDN 1102, MDN 1103 , MDN 1104 , MDN 1201 , MDN 1202, MDN 1203, MDN 1204 , MDN 1206, MDN 1208, MDN 1209, MDN 1211 , MDN 1213 (esp. cardiac and vascular implants including valves, grafts and stents; dental implants and non-implantable dental materials; surgical meshes and soft-tissue implants; intraocular and contact lenses; ophthalmic solutions and surgical instruments; respiratory masks and gas administration tubes including endotracheal and tracheostomy tubes; wound closure devices such as sutures and staples; adhesion barriers and cystic solutions; dermal fillers and other implantable devices) For Product Reviewers for Devices with Specific Characteristic MDS Codes: MDS 1001, MDS 1008, MDS 1005 (EO, Moist Heat, Radiation and Aseptic sterilization) Role Overview Site Auditors Conduct QMS audits under EU MDR Assess manufacturing and supplier compliance Prepare audit reports and findings Collaborate with technical reviewers and decision makers Product Reviewers Perform EU MDR technical documentation assessments Participate in conformity assessment activities Work closely with clinical experts and internal teams Education Requirement At least a B.Sc. degree in Engineering, Medicine, Pharmacy, Pharmaceuticals, Biochemistry Competency Requirements Minimum 4 years professional experience in medical devices or related sector Quality management experience (for auditors) Technology/device-specific experience within relevant code OR Participation in conformity assessments / multiple technical documentation reviews For sterilization (MDS 1005): experience in EO, moist heat, radiation, aseptic processes or cleanroom auditing is required.

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