Cure Talent is delighted to be working with an innovative MedTech company revolutionising ear and hearing healthcare! With their ongoing growth and exciting projects, we have a fantastic opportunity for a QA Specialist to join their highly motivated team on an initial 9 month contract. As a QA Specialist, you will play a key role in maintaining and continuously improving the ISO 13485 QMS. You will oversee Quality Events, CAPAs, Change Controls, and Quality Metrics while supporting compliance with QSR, ISO, CE, and other global regulatory requirements. Key Responsibilities: Maintain and improve the ISO 13485 QMS. Oversee Quality Events, including deviations, non-conformances, CAPAs, and Change Controls. Generate and revise SOPs and associated documentation. Support regulatory compliance activities, including audits, customer complaints, and employee training. Generate and maintain Design History Files and Technical Documentation to support global market registrations. Participate in risk management activities, ensuring effective risk mitigation in products and processes. The Ideal Candidate Will Have: BSc in Science or a related field. Proven Quality Assurance experience within the Medical Device industry. Strong working knowledge of ISO 13485, FDA 21 CFR Part 820, and EU MDR. Experience with EN 62304 (desirable). Certified Internal or Lead ISO 13485 Auditor. Experience using an eQMS. If you''re looking for an exciting opportunity to be part of a rapidly expanding ..... full job details .....