Software Quality Assurance Engineer – Medical Devices
We are seeking a proactive individual with experience in designing and implementing software quality assurance systems and software development processes in a regulated environment to assist in the translation of our research. This is an exciting opportunity to work on novel software solutions in collaboration with clinicians and engineers in a clinical academic setting.
The primary role of the post holder will be to guide application of regulatory, quality and safety standards of different project teams in the CME to develop healthcare software as medical devices for release to the clinic to be used in first-in-human studies and follow-up clinical investigations. Emphasis will be given on the implementation of flexible and agile development processes that can meet the varied requirements of academic research projects as they progress along the translational pathway.
The individual will be expected to identify gaps in information and processes; recommending solutions, and be responsible for setting standards and developing procedures that meet the needs of different groups across the CME.