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MyOme

Clinical-grade genome sequencing for disease risk

Machine Learning Engineer

Applied Machine LearningConfirmed live in the last 24 hours
Full-timeMenlo Park, CA, USA

About the Job

Requirements

  • A master's or PhD in computer science, statistics, biomedical informatics, bioengineering, or a related field, or equivalent experience, is required; a PhD is preferred.
  • At least 5 years of experience developing machine-learning and deep-learning models, including at least 3 years with models in production.
  • Strong machine-learning fundamentals, including supervised learning, survival analysis (Cox and deep survival models), calibration, class imbalance, leakage and cohort shift, and evaluation using AUROC, C-index, calibration curves, and decision curves.
  • Advanced deep-learning model development experience designing, training, and debugging modern architectures in PyTorch, including transformers, sequence and temporal models, multimodal fusion, and deep survival models, with a record of models outperforming strong baselines.
  • Rigorous experimental practice, including ablations, hyperparameter search, regularization, overfitting control, reproducibility, and comparison against baselines.
  • Production machine-learning engineering experience with packaging, APIs, containers, CI/CD, testing, model versioning, and monitoring.
  • Experience building and evaluating LLM-based systems using prompting, tool use and agents, retrieval, and structured extraction, with quantitative evaluation.
  • Strong Python and SQL skills, comfort with large tabular datasets, and experience with cloud environments such as GCP or AWS.
  • Ability to explain model behavior to clinicians and product partners.

Responsibilities

  • Develop and improve deep-learning risk models through architecture design, multimodal EHR and genomics fusion, temporal and sequence modeling of patient histories, deep survival models, representation learning, ablation, and benchmarking.
  • Productionize disease-risk models as versioned bundles containing model weights, survival-model coefficients, calibration, and PRS scaling, with reproducible training and a model registry.
  • Build and maintain inference services using Python, FastAPI, and Docker, and integrate them with reporting and data platforms.
  • Implement calibration, recalibration to new populations, and score reporting for absolute risk over defined horizons, percentiles, and risk tiers.
  • Deploy monitoring for calibration, discrimination, input drift, and coverage, with defined retraining triggers.
  • Run and automate external validation on partner datasets in secure environments.
  • Coordinate model evaluation at clinical trial sites with the hiring manager, including site data intake, harmonization, evaluation runs, and results reporting.
  • Apply LLMs and agentic methods where they add measurable value, including structured extraction from clinical notes, automated evaluation, and guardrailed explanations of results.
  • Produce validation reports, model cards, and change-control documentation to support CLIA and regulatory review.

Desired Qualifications

  • Experience with EHR data, including OMOP, ICD, LOINC, RxNorm, and temporal features; experience with All of Us, UK Biobank, or health-system data is especially useful.
  • Familiarity with polygenic risk scores or statistical genetics.
  • Experience in regulated environments, including CLIA, CAP, HIPAA, FDA SaMD, or design controls.
  • Experience with MLOps tools such as MLflow, Airflow, Prefect, or Kubernetes.
  • Publications or shipped products in clinical machine learning.

About the Company

MyOme

Clinical-grade genome sequencing for disease risk

MyOme provides clinical-grade whole genome sequencing to assess disease risk for individuals and families. It uses comprehensive genome data combined with AI and machine learning to generate integrated disease risk scores that update over time as lifestyle changes occur, delivering actionable insights for lifelong health management. The company differentiates itself by offering a single, detailed genetic test that yields evolving, lifetime risk evaluations rather than a one-off report, targeting both common and rare diseases. Its goal is to enable earlier health interventions and better disease management through personalized, data-driven genetic information.

Company size
51-200
Company stage
Series B
Total funding
$23M
Headquarters
Palo Alto, CA
Founded
2017

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