Quality Engineer

Quality Engineer£40 - £50 Outside IR35 6-month contract OnsiteWest MidlandsiO Associates are seeking a Quality Engineer who is highly experienced in the Medical Device industry for a leading client of ours based in the West Midlands.The role itself will entail reviewing/creating requirements and specifications, validation protocols and reports, risk management documentation, and design change records. In addition, the role will support CAPA processes and non-conformance management.Key Skills:In-depth knowledge of ISO 13485 and 21 CFR Part 820 Quality System Regulations5 + Years of experience in a Quality Engineering role within the medical device industryProficient in using risk management tools plus techniques in compliance with ISO 14971Design and DevelopmentChange control processValidation activitiesCAPA Root Cause InvestigationsIf you are interested, please apply with your most up-to-date CV or contact me via email: o.westwood @ ioassociates.co.uk, or call 01172840468