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Salary: USD 118,150 - 167,475 / annual
Freenome is seeking a Technical Product Manager III to join the Product Management team, reporting to the Associate Director of Technical Product Management. This role is responsible for planning and executing engineering initiatives for the Commercial Data Platform and Data Products, ensuring efficiency, scalability, and usability across Commercial, Laboratory, and R&D teams.
Key responsibilities include:
• Define requirements and manage development processes, systems, and software infrastructure for the data platform and tools supporting Commercial and R&D initiatives
• Partner with laboratory and business stakeholders to understand requirements, optimize workflows, and lead data platform and product definition while ensuring alignment with regulatory standards (HIPAA, HITECH, FDA, CAP/CLIA)
• Translate product requirements into Epics and Stories with clear user acceptance criteria in collaboration with engineering teams
• Track and drive development using issue tracking systems (e.g., Jira) to ensure fulfillment of requirements
• Lead and facilitate productive interactions between users and engineers to ensure user needs are understood and met
• Create and operationalize a comprehensive technical strategy and integrated roadmap for data products, pipelines, and tooling
• Align cross-functional milestones and deliverables across current and future programs
• Provide clear vision for future development efforts with scalability and accessibility in mind
• Ensure complete data integrity throughout the pipeline with technical and process-oriented solutions
The role is remote-based with occasional onsite travel to headquarters in Brisbane, California as needed.
REQUIREMENTS:
• Bachelor's degree in an analytical, technical, or scientific field; advanced degree preferred
• At least 5 years of experience in a software development environment, ideally within biotechnology and NGS (Next-Generation Sequencing)
• Deep expertise in identification and prioritization of software features
• Demonstrated ability to successfully lead complex trade-off decisions between functions and measurably improve organizational success and processes
• Experience leading software development efforts to meet regulated market standards (FDA, CAP/CLIA), laboratory operations, medical affairs, or clinical study operations for diagnostics
NICE TO HAVES:
• Experience building solutions with a focus on multiomics, NGS, or proteomics
