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Experience working with early-stage products. Experience developing approval ready devices and products. Experience with C++ & C also useful. Experience within Medical Devices Sector (ISO 13485). If interested, please apply, or reach out for further information about the role more »

is compulsory Knowledge of design control, risk management, root cause investigation methods, process validation, statistical process control (SPC), protocol/report preparation. Knowledge of ISO 13485, European Medical Device Regulation and FDA 21 CFR 820 requirements, understanding the medical device regulatory environment and requirements Familiar with QMS processes more »