Technical Product Manager

Tempus AI; Stati Uniti; Remoto; USD 85.000 - 110.000; Tempo pieno

Descrizione del lavoro

Ambry Genetics is seeking a Technical Product Manager to partner with the Integration Engineering team. You will own the software lifecycle for Genomic Tertiary Analysis and Reporting tools, translating complex clinical genetics needs into actionable requirements and Jira tickets.

You’ll guide SDLC from discovery through validation and report status to stakeholders. The role bridges clinical genetics, bioinformatics, and software engineering, driving vision, intake, and execution for variant

Competenze

• Bachelor’s degree in CS or related field.
• 3+ years in technical product management or related role.
• Strong written and verbal communication.
• Experience using JIRA.
• Knowledge of AGILE/SCRUM and SDLC.

Mansioni

• Write clear user stories documenting functional and technical requirements with stakeholders and PMs.
• Collect, synthesize, and document artifacts to clarify software specs for teams.
• Research and solve software issues with stakeholders and technical team.
• Report project status to PMO, product managers and lead TPM.
• Develop solutions with leads/subject matter experts aligning to business goals.
• Identify upstream/downstream impact with other TPMs.
• Coordinate with QAs to test features against requirements during validation.
• Coordinate change control protocols for production deployments.

Conoscenze

Communication skills

JIRA proficiency

SDLC knowledge

Agile SCRUM

Requirements gathering

Use case documentation

Software product management

Formazione

Bachelor’s degree in Computer Science, Biomedical Sciences, Molecular Biology, Genetics

Strumenti

JIRA

Descrizione del lavoro

Compensation:

US Range: $85,000 - $110,000

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).
  

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