> Markdown version of [/jobs/ext/3957219-scientific-product-owner-qdi](https://www.wearedevelopers.com/jobs/ext/3957219-scientific-product-owner-qdi). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Scientific Product Owner, QDI - **Company:** Qiagen Gaithersburg, Inc. - **Location:** Los Angeles, CA, United States - **Salary:** $120,000.0 - $165,000.0 - **Contract:** Permanent contract - **Skills:** Application Programming Interfaces (APIs), Agile Methodology, Confluence, JIRA, Hospital Information Systems, Databases, Scrum Methodology, Software Engineering, Software Requirements Analysis - **Published:** October 27, 2026 - **Apply:** https://www.careerbuilder.com/job-details/scientific-product-owner-qdi-los-angeles-ca--a601c8ad-03d2-4856-bb24-a5dedca863ab ## About the Role Entrepreneurship, Healthcare, Diversity, Genomics, Clinical Information Systems, Writing Skills, Acceptance Testing, Disease, Cancer, Customer Relations, * MS or PhD in genetics, molecular biology, genomics, or a related life science, with expertise in cancer and/or hereditary disease. * Preferred: 2+ years interpreting clinical next-generation sequencing (NGS) data in a clinical lab, research, or testing environment. * Working knowledge of variant classification guidelines (e.g. ACMG/AMP) and common genomic data formats and databases. * 1+ year in a product owner, business analyst, or requirements role on a software or bioinformatics product, or equivalent hands-on experience writing specifications for developers. * Familiarity with agile development (Scrum or Kanban) and tools such as Jira, Confluence, and requirements-management systems. * Preferred: comfort discussing APIs, data models, and system behaviour with engineers (no software engineering background required). * Excellent written and spoken English, including scientific and technical writing. * Collaborative team player who can coordinate work across functions and across US and European time zones. * Attentive to detail, curious, and comfortable with complex scientific, technical, and regulatory topics. ## Description * Own the product backlog for assigned releases: write and refine user stories and acceptance criteria so work is ready for development. * Translate scientific needs from product managers, content scientists, key opinion leaders, and customers into clear software requirements. * Be the scientific voice for engineering: lead refinement sessions and resolve domain questions quickly so the team stays unblocked. * Shape scientific design for hereditary and somatic workflows with product management and content science teams. * Work with engineers on how scientific content, variant annotation, and classification logic flow through the platform. * Test new features from a scientific user's perspective and confirm requirements are fully covered. * Prioritize customer-reported issues and enhancement requests by clinical impact. * Assess reported issues for severity, patient safety, and usability risk in our IVD clinical decision-support product. * Maintain design control documentation and support release readiness, including release notes, user guides, and training for field application scientists and support teams, within an ISO 13485 quality system. * Act as scientific subject-matter expert and contribute to roadmap planning.