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The Quality Engineer is responsible for implementing quality assurance principles for the development and maintenance of medical devices. This includes risk management, quality assurance reviews, documentation planning, participation in audits, investigations of quality events, and support in process validation and change management activities.

As a Senior Quality Engineer, you will lead the verification and validation of medical device systems, develop compliance documentation, manage risk assessments, and provide guidance in Computer System Validation, ensuring adherence to FDA regulations and industry standards. You'll engage in collaborative efforts, supporting quality assurance processes and training team members.

As a Software Engineer on the Tempus Next Cardio team, you will develop and release AI-enabled software aimed at identifying patients with gaps in clinical care. You will collaborate with cross-disciplinary teams to create performant and maintainable software solutions, utilizing a modern tech stack.

The Senior Manager, Quality Engineering is responsible for overseeing postmarket surveillance activities, ensuring compliance with FDA and ISO regulations, managing complaint handling processes, and collaborating with cross-functional teams for product lifecycle management and quality assurance. This role involves creating procedures for monitoring product safety and effectiveness, leading investigations into complaints, and providing training and guidance on regulatory processes.

The Program Manager will oversee the cross-functional planning and execution of new assay launches within Genomics, managing work streams, ensuring documentation standards, and aligning with strategic objectives. Responsibilities include facilitating communication across teams, driving project accountability, and maintaining operational excellence in complex project environments.

The Senior Process Manager will collaborate with various teams to support assay launches and process improvements in clinical testing. Responsibilities include managing project issues, reporting status, proposing workflows, and maintaining stakeholder communication on projects.

The Operations Manager will lead cross-functional planning and execution of new assay launches, focusing on oncology. This role involves collaborating with various teams, managing stakeholder communication, and implementing continuous improvements to operational workflows. The manager will also oversee the project plan for assay development and may eventually supervise a team.