Elephas is developing a unique diagnostic device that measures how a patient’s own tumor cells respond to cancer therapies. We are harnessing the latest advances in cancer biology, multimodal microscopy, engineering, and artificial intelligence to revolutionize cancer treatment.   While the system is being designed to help determine the best cancer therapy for each patient, there will be significant potential applications of the platform for biopharma companies developing oncology drugs and for cancer researchers.

Sep 24, 2021
Summary Elephas, a Madison, WI-based biotechnology company, is seeking a highly motivated Quality/Regulatory Engineer with a focus on Software as a Medical Device (SaMD) to join our QA/RA team. A successful candidate will have a bachelor’s degree and be pursuing a career in Quality Assurance or Regulatory Affairs. This candidate will be self-motivated to learn and be comfortable in a fast-paced and highly collaborative environment. As a Quality/Regulatory Engineer at Elephas you will closely collaborate with a cross-functional team of Engineering, IT, and Product Management as you build and improve the Quality Management System (QMS).   Essential Duties and Responsibilities This position is an integral member of the QA/RA team . In this role, you will be responsible for ensuring documentation (e.g., DHF) and records within the QMS are complete and support development of software as/for/in a medical device application. Drive requirements of the FDA Quality System...
Elephas Bio Full time