Job Title: Quality Assurance and Regulatory Affairs Specialist Location: Corsham, Wiltshire Hours of Work: Monday to Friday, 8.30am to 5pm Salary: Negotiable: circa £37,000 depending in experience Holiday and Benefits: 25 days plus bank holidays, company pension scheme.Are you passionate about quality, compliance, and making a real impact in the medical device industry? We''re looking for a Quality Assurance and Regulatory Affairs Specialist to join our team and help ensure that our products meet the highest standards of safety and performance.This is an exciting opportunity to work in a dynamic environment where innovation and quality are at the heart of everything we do. You''ll play a key role in ensuring compliance and driving improvements that make a difference worldwide. About the Role In this role, you''ll support the Quality and Regulatory team in maintaining compliance with medical device and IVD standards and regulations. You''ll monitor and advise on the performance of the Quality Management System (QMS), produce reports on key indicators, and drive continuous improvement initiatives across the organisation. Key Responsibilities Implement, maintain, and improve the Quality Management System in line with applicable standards and regulations.Monitor and report on quality performance, including tracking key performance indicators (KPIs).Contribute to regulatory submissions, technical documentation, and product registrations.Provide guidance on compliance with E