Quality Manager Excellent opportunity for a Quality Manager to join a growing and innovative company. The Quality Manager will be responsible for the management of quality systems, quality aspects of internal manufacturing and also overseeing sub-contract manufacturing partners and support of internal projects. Key Responsibilities: Maintain company's Quality Management System (QMS) and report on the performance of the QMS to the company's Senior Management Team Supervision of Quality Technicians and Quality Engineers. Lead quality personnel in the completion of required departmental activities including objectives/ goals. Quality system oversight: management reviews, quality review and internal audit programme Supplier control including: supplier audits, SCARs, performance monitoring and quality agreements Manufacturing validation including: MVP development, PFMEAs, validation protocols and reports Customer complaints: approval of analysis reports and analysis of complaint trends. CAPA/NCR: oversight of the investigation and timely closure of CAPA and NCRs External audits: lead the company in regulatory agency quality management system audits including FDA and Notified Body Key Requirements: Bachelor Degree in a relevant discipline required with 4 years relevant experience in a similar role Experience in the Medical Devices Industry is essential Demonstrated knowledge of ISO 13485 and 21 CFR 820 requirements Ability to work as part of a team and meet targets/goals efficiently. Excellent interpersonal & communication skills essential Strong knowledge of quality principles and the ability to utilize these methods in development and manufacturing environments For further information please contact Loretta Flynn Skills: Quality Manager Quality Lead ISO 13485 21 CFR 820