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As a Sr. Computer System Validation Quality Engineer at Tempus, you will play a crucial role in ensuring the quality and compliance of our medical device systems. You will lead the verification, validation, and maintenance of host and computer systems that support Tempus Medical Devices. Your expertise will be essential in conducting risk assessments, developing testing strategies, and ensuring adherence to regulatory standards such as FDA Quality System Regulation, ISO 13485, and GAMP5. You will also be responsible for leading computer system validation activities for AI applications and software tools, ensuring they meet user, functional, and regulatory requirements.
