Job Description The successful candidate will be responsible primarily for planning and conducting audits of in-vitro diagnostic medical devices to EU IVDR (EU Regulation 2017/746 ). The role will also include auditing to EU MDR (EU medical device regulation 2017/745), UK MDR 2002 for medical devices and IVD’s, ISO 13485 and MDSAP, enabling the delivery of assessment and certification services that meet customer, regulatory and accreditation requirements. Training to enable qualification under all schemes will be provided. Summary of role: Job Title: IVD / Medical Device Lead Auditor Hours: 37.5 hours per week Job Location: Field-based (UK) Travel: Mainly within the UK, a Company car or car allowance provided Bonus scheme Salary: From £65,000 Depending on Experience Key Accountabilities: Conduct audits at customers’ sites using established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Work alone or lead audit teams as appropriate, enhance customer satisfaction and ensure compliance with standards and regulatory requirements. Complete all work within the required budget and timeframes Complete specific projects about medical device procedures, processes, systems and documentation as requested by the Medical Devices Manager