Senior Bioinformatics PM - Regulated Diagnostics

Tempus AI; Chicago (IL); On-site; USD 105,000 - 145,000; Full time

Benefits offered by this job

Incentive compensation

Restricted stock units

Medical benefits

Job summary

Tempus AI in Chicago, IL is seeking a Senior Technical Product Manager for Bioinformatics to lead software product development in cancer genomics and translational research. You will coordinate with regulatory and quality teams, manage the software lifecycle, and champion data-driven decisions across oncology projects.

Experience with diagnostic products and FDA/EU IVDR familiarity is preferred. Strong collaboration across interdisciplinary teams is essential as you report to the Head of

Qualifications

• Bachelor's or MS in a scientific discipline.
• Significant experience in medical device development and regulatory submission.
• 2-4 years relevant experience in diagnostics product development.
• Familiarity with US FDA and EU IVDR regulatory frameworks.

Responsibilities

• Managing software development lifecycle processes.
• Engaging with the quality and regulatory team and supporting quality processes.
• Incident management: promptly triage, coordinate, and manage resolution of issues.
• Stakeholder support: provide dedicated and responsive support to all stakeholders using the bioinformatics software.
• Feature request intake and prioritization: collect, prioritize, and manage feature requests to guide software development.
• Interfacing with Product Managers of downstream engineering teams during implementation.
• Data contract management with downstream engineering teams.
• Documentation: maintain comprehensive and up-to-date documentation for all bioinformatics software.

Skills

Medical device development

Regulatory submissions

FDA regulatory knowledge

Education

Bachelor's or MS in a scientific discipline

Job description

Tempus AI in Chicago, IL is seeking a Senior Technical Product Manager for Bioinformatics to lead software product development in cancer genomics and translational research. You will coordinate with regulatory and quality teams, manage the software lifecycle, and champion data-driven decisions across oncology projects.

Experience with diagnostic products and FDA/EU IVDR familiarity is preferred. Strong collaboration across interdisciplinary teams is essential as you report to the Head of