engineering
Posted YesterdayVP, Product Engineering, Genetics Portfolio
at Natera
United StatesRemote
Responsibilities
- Define and own the multi-year software roadmap for the Genetics portfolio, including Women's Health, Organ Health, and Emerging Business / Rare Disease Diagnostics, ensuring alignment with clinical utility and revenue targets.
- Lead the Digital Product Management team to translate complex clinical needs into technical requirements, prioritizing the backlog for maximum patient and business impact.
- Drive the strategy for Product Integration, ensuring a frictionless ordering and reporting
- Collaborate with R&D and Laboratory Operations to ensure new assays—including those for emerging and rare disease markets—are launched with "automation-first" software that reduces manual burden.
- Track and report on portfolio-specific KPIs, including product performance, user adoption, and delivery velocity. Leadership & Team Development
- Lead and mentor a specialized team of Product Solution Architects and Integration Engineers, fostering a culture of technical rigor and business empathy.
- Bridge the gap between scientific complexity (Genetics, Bioinformatics) and digital product simplicity, ensuring tools are intuitive for clinicians and internal lab staff.
- Manage the organizational transition from technology-focused component teams to mission-oriented cross-functional pods. Regulatory & Clinical Quality
- Ensure all software products meet the stringent
- requirements and design controls are properly documented to support successful audits and submissions.
Requirements
- experience that positions Natera as the market leader in reproductive, renal, and rare disease health. Key
- experience across provider portals and EMR systems, Accessioning/LIMS, Lab Workflow Tracking, Bioinformatics Pipelines, and Tertiary Analysis and reporting systems.
- requirements of a CLIA/CAP-certified and FDA-regulated environment.
- experience in software product engineering or technology leadership, with a significant background in Clinical Genomics, Diagnostics, or Rare Disease.
- Deep understanding of the software infrastructure (LIMS, Portals, EMR) required to support high-volume genetic testing at scale.
- Experience in product life cycle management, including supporting the commercialization of new diagnostics and driving continuous improvement for on-market products.