Job Title: Regulatory QMS Specialist Job Type: Permanent, full-time position Location: Bourton on the water, Gloucestershire, UK – Hybrid (3 days on site) Remuneration: £35,000 - £40,000 An exciting Regulatory QMS Specialist position working for a global leader in the provision of quality medical products. The role will be working across a wide product portfolio including orthopaedic products. Responsible for managing the audit program, including internal auditing and supplier auditing. Supporting the Quality Management System, including Quality Objectives and NC/CAPA management. Role responsibilities: Manage the supplier auditing program, including scheduling audits and assigning auditors. Perform supplier audits as required. Manage the internal audit program, including scheduling audits and assigning auditors. Perform internal audits as assigned. Provide support during external audits, including collating pre-audit document requests. Manage the Quality Objectives procedure. Manage the NC/CAPA procedure. Provide backup to the RA/QMS Administrator for document control and training activities on MasterControl. Continuous improvement - To initiate, support and lead Continuous Improvement projects as required. Qualifications Required: Experience of Quality Systems auditing is essential. Experience within the Medical Devices industry is desirable. Excellent working knowledge of Microsoft Office (Word, Excel, OneDrive.) Excellent written and oral communication skills in English. This is a great opportunity to join a leading business who specialise in orthopaedic products. Please note this is a hybrid position that will require 3 days on site per week. For more information, please reach out to lucy.kirkaldycpl.com