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Tempus is seeking a Senior Quality Engineer (Software Design Controls) to join our Quality Assurance (QA) group. This role will involve quality management system (QMS) and software development life cycle (SDLC) activities, ensuring compliance with FDA's Quality System Regulation (QSR), ISO 13485, and other applicable regulatory requirements. The successful candidate will support Tempus' SDLC activities for medical device software and Software as a Medical Device (SaMD), maintain relevant procedures, and ensure that required documentation and DHF deliverables are generated and maintained throughout the SDLC.