Jobs at Veracyte

Lead design and development of MRD NGS-based LDTs from concept through analytical validation. Build and maintain production-ready bioinformatics pipelines, design and analyze validation studies, optimize variant detection and error suppression, ensure CAP/CLIA/FDA/IVDR compliance, support regulatory submissions, and mentor junior scientists while collaborating cross-functionally with wet-lab, clinical, QA/RA, and software teams.

Lead design, development, and validation of bioinformatics workflows for regulated NGS diagnostics. Develop scalable AWS/containerized pipelines, apply ML/statistical methods for assay optimization and validation, coordinate cross-functional project delivery, support regulatory submissions (CAP/CLIA, FDA, IVDR), mentor junior staff, and collaborate with infrastructure, engineering, and quality teams to deploy production-grade analysis pipelines.

This role involves analyzing EHR and insurance claims data to define clinical outcomes, developing AI models, and collaborating with technical experts for manuscript preparation.

Lead transformation of the Product Development Process into a scalable PMO, oversee enterprise portfolio governance, intake and prioritization, capacity planning, stage-gate decisions, and launch readiness. Standardize templates, dashboards, KPIs, and risk tracking; prepare executive and Board communications; partner across functions (R&D, Product, Quality, Regulatory, Commercial); and build and lead a high-performing PMO team.

The Director of Data Engineering leads the development of data platforms to support analytics in cancer care, overseeing architecture and engineering while mentoring a team.

Field-facing role promoting Veracyte genomic diagnostic tests to clinicians and health systems. Develop and execute territory plans, establish clinical collection and ordering protocols, grow and maintain accounts, navigate complex health systems, and collaborate internally. Regular travel and quota-driven sales responsibilities.

Supports development and validation of NGS-based minimal residual disease assays through molecular biology experiments, sample preparation, PCR, library preparation, documentation, data analysis, troubleshooting, and technology transfer. Maintains laboratory supplies and records while collaborating with product development, clinical laboratory, automation, and operations teams. The role requires accurate execution of protocols in a regulated, fast-paced laboratory environment.

Develops and executes sales training programs for Prosigna commercial teams, including new-hire onboarding, advanced training, classroom and virtual instruction, ride-alongs, competency assessments, and performance feedback. Partners with Marketing, Sales, and Medical Affairs to align training with commercial strategy, products, and market needs. Creates compliant training materials, manages MLR approval, evaluates program effectiveness, and leads training for other business-unit hires. Travel is required for in-person training.

Lead an engineering team building AI-powered, cloud-native billing automation for laboratory revenue cycle: design scalable APIs, integrations, AI features (IDP, RAG, agents), ensure compliance, partner with stakeholders, drive CI/CD, IaC, observability, hiring and team development.

Lead a Quality Engineering Platform team to build scalable test automation frameworks, self-service quality platforms, and AI-enabled testing tools. Define quality strategy, embed shift-left practices, integrate testing into CI/CD, ensure regulatory compliance for diagnostic software, and drive engineering metrics and developer enablement.

Lead regional commercial marketing for Veracyte's IVD oncology portfolio across EMEA. Translate market insights into regional strategy, support product lifecycle and launches, run VoC and competitive research, oversee multi-channel campaigns, content governance, events, sales enablement, distributor strategy, budgeting, compliance, and cross-functional alignment to drive adoption, demand generation, and market leadership.

Lead strategy, development, and operation of LIMS and lab pipelines teams to deliver scalable, compliant laboratory software and sequencing secondary-analysis workflows. Align engineering with lab operations, bioinformatics, product, quality, and regulatory to ensure traceability, auditability, and data integrity. Drive platform modernization, CI/CD, observability, and cloud-native practices while recruiting, developing, and retaining high-performing teams.

Execute and analyze experimental studies to develop, optimize, verify, and transfer NGS-based MRD assays. Prepare and qualify clinical/contrived samples, support automation and high-throughput workflows, maintain documentation and SOPs, troubleshoot assays, and collaborate cross-functionally to enable clinical laboratory implementation and validation.

Lead development and clinical implementation of NGS-based MRD assays, designing and executing feasibility, optimization, and verification studies. Drive workflow automation, QC, throughput, and LIMS integration; author regulatory documentation and SOPs. Serve as SME for NGS, oncology genomics, and ctDNA technologies while collaborating cross-functionally and mentoring laboratory personnel to support technology transfer and commercialization.

Perform high-complexity molecular genetic testing, review and report patient results, conduct QC/QA and proficiency testing, prepare reagents, troubleshoot assay issues, support validations/research, and comply with regulatory and safety requirements.

Lead development of digital pathology AI models using whole-slide image data to predict clinical outcomes and morphologic features. Drive dataset selection and annotation, coordinate and mentor junior scientists, partner with bioinformatics, statistics, and clinical experts, produce analyses and visualizations for publication, and manage cross-team project execution to build diagnostic products.

Manage complex pre- and post-service appeals (Level 1–2 and external review), serve as clinical SME on payer medical policy, own end-to-end case resolution, mentor junior staff, analyze denial patterns, improve SOPs and appeal assets, coordinate with providers, and support digital transformation and cross-functional reimbursement initiatives.

Lead a team to design, develop, optimize, and scale NGS enzymes, buffers, and reagents for clinical lab use. Oversee V&V, CQAs, stability testing, and design control documentation while ensuring GMP/ISO 13485 and CLIA/CAP compliance. Drive cross-functional design transfer, manufacturing scale-up, and quality oversight to support internal high-throughput diagnostic workflows.

Lead LIMS administration and enhancements for regulated clinical labs. Manage a team, oversee validation, integrations, upgrades, governance, and vendor relationships. Partner with Operations, Engineering, and Quality to ensure compliant, scalable systems, drive automation and process improvements, and support multi-site laboratory growth.

Senior individual contributor responsible for system architecture, reliability, and operability of a Windows-based IVD software product. Design and support deployments (IIS, SQL Server, WSL, Docker) across on-prem, virtualized, and cloud environments. Lead root-cause analysis, define supported deployment models, improve CI/CD and observability, automate configuration, apply security best practices, and ensure regulatory/quality compliance while mentoring responses to system-level escalations.