Technical Product Manager

Tempus AI

California

On-site

USD 85,000 - 115,000

Full time

32 hours ago
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Job summary

Tempus AI is seeking a Technical Product Manager to lead the integration engineering software lifecycle for genomic data tools. You will define system requirements for clinical genetics software, oversee SDLC from discovery to validation, and communicate technical requirements to stakeholders.

The role requires bridging clinical genetics, bioinformatics pipelines, and software engineering to empower variant interpretation and final report generation.

Qualifications

  • Bachelor degree in CS/biomedical sciences or related field.
  • Advanced degree preferred.
  • Experience with SDLC and agile methodologies.
  • Proven ability to document use cases and gather requirements.

Responsibilities

  • Write clear user stories to document functional and technical requirements with stakeholders and product managers.
  • Collect, synthesize, and document artifacts to clearly communicate software specifications within teams.
  • Research and solve software issues by partnering with stakeholders and technical team.
  • Report project status updates to PMO, product managers and lead TPM.
  • Collaborate with technical leads and SMEs to align solutions with business logic and feasibility.
  • Coordinate with other TPMs to identify upstream/downstream impacts for a project.
  • Work with QA to test and validate features against requirements and assist end-user validation.
  • Coordinate change control protocols for production deployments.

Skills

Strong communication
SDLC knowledge
AGILE & SCRUM
Use case documentation
Requirements gathering
3+ years software analysis
3+ years TPM/PO in genetics

Education

Bachelor's degree in Computer Science, Biomedical Sciences, Molecular Biology, Genetics, or related specialization
Advanced degree

Tools

JIRA

Job description

Role Overview

As a Technical Product Manager working with the Integration Engineering team, you will analyze and define system requirements to support the software products in the clinical genetics domain area. The TPM will oversee the software enhancements through the entire SDLC, from discovery, design, development, and validation. The TPM is responsible for communicating technical and functional requirements with stakeholders and users, creating Jira tickets detailing requirements for the scrum teams, overseeing the deliverable timeline to be met, and reporting project status updates upon request. You will have the opportunity to create innovative solutions and leverage the latest technologies to make our diagnostics-testing even better. For this role, we are seeking a domain-expert to own and drive the software product lifecycle for our Genomic Tertiary Analysis and Reporting applications. The ideal candidate will bridge the gaps between complex clinical genetics, bioinformatics pipelines, and software engineering. You will be primarily responsible for the vision, intake, and execution of tools that ingest processed genomic data and empower clinical scientists to perform variant interpretation, clinical curation, and final report generation. The ideal candidate possesses a rare blend of deep technical software management skills and a strong foundational understanding of clinical variant analysis

Compensation

US Range: $85,000 - $115,000

Role Overview

As a Technical Product Manager working with the Integration Engineering team, you will analyze and define system requirements to support the software products in the clinical genetics domain area. The TPM will oversee the software enhancements through the entire SDLC, from discovery, design, development, and validation. The TPM is responsible for communicating technical and functional requirements with stakeholders and users, creating Jira tickets detailing requirements for the scrum teams, overseeing the deliverable timeline to be met, and reporting project status updates upon request. You will have the opportunity to create innovative solutions and leverage the latest technologies to make our diagnostics-testing even better. For this role, we are seeking a domain-expert to own and drive the software product lifecycle for our Genomic Tertiary Analysis and Reporting applications. The ideal candidate will bridge the gaps between complex clinical genetics, bioinformatics pipelines, and software engineering. You will be primarily responsible for the vision, intake, and execution of tools that ingest processed genomic data and empower clinical scientists to perform variant interpretation, clinical curation, and final report generation. The ideal candidate possesses a rare blend of deep technical software management skills and a strong foundational understanding of clinical variant analysis

Responsibilities
  • Write clear user stories to document clearly on functional and technical requirements by collaborating with stakeholders and product managers;
  • Collect, synthesize, and document other project related artifacts to ensure software specifications are clearly communicated within the internal and external teams;
  • Research and solve software issues by partnering with stakeholders and technical team;
  • Report project status updates to PMO, product managers and lead TPM;
  • Work with technical leads and subject matter experts to develop solutions that align with defined business logic, goals, and objectives, and determine the technical and operational feasibility of said solution;
  • Collaborate with other TPMs to identify upstream and/or downstream impact for a given project;
  • Work with QAs to test and validate developed features against requirements and be a resource during end user validation.
  • Coordinate change control protocols that ensure the business approval of production deployments.
Preferred Qualifications
  • Bachelor's degree in Computer Science, Biomedical Sciences, Molecular Biology, Genetics, or related specialization required.
  • Advanced degree preferred.
  • Strong verbal and written communication skills.
  • Professional knowledge and experience using JIRA.
  • Experience facilitating project meetings, requirements gathering, and follow-ups.
  • Solid understanding of the Software Development Life Cycle (SDLC).
  • Knowledge of AGILE and SCRUM methodologies.
  • Proficiency in gathering requirements and documenting Use Cases.
  • 3+ years of analysis experience in a software application development environment.
  • 3+ years as a Technical Product Management, Technical Product Owner, or Business Systems Analyst in a clinical genetic testing lab, molecular diagnostics company, or digital health platform (preferred).
PRIVACY NOTICES

To review Ambry’s Privacy Notice, Click here: https://www.ambrygen.com/legal/privacy-policy

To review the California privacy notice, click here: California Privacy Notice | Ambry Genetics

To review the UKG privacy notice, click here: California Privacy Notice | UKG

Equal Opportunity Employer

This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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