Quality and Compliance Co-Ordinator 13485 MDR

This role will join an established Quality team, providing technical support on Quality and Compliance, in adherence to 13485 and MDR.

Client Details

Our client is a leading Medical Device business, operating nationally. This business provides various technical services to a broad range of Medical Tech/Device clients across the UK and internationally.

Description

- Oversight of QMS

- Ownership of Compliance focused work, ensuring business processes are in adherence to ISO 13485 and MR/ EU MDR

- Training across the business areas, to create a positive Quality culture

- Manage documentation relating to Quality and Compliance

Profile

- Experience within a 13485 regulated business

- Good exposure to Quality and Regulatory function

- Great communicator, able to influence and manage stakeholders internally

Job Offer

- Competitive basic salary + benefits

- Hybrid working, 2 days at home