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Guardant Health

FDA-approved blood-based cancer diagnostics provider

Staff Automation Engineer

Controls & Automation EngineeringUpdated on Nov 14
Full-timePalo Alto, CA, USA$136.4k - $220.7k /yrIn-person

About the Job

Requirements

  • A BS in engineering or science with at least 8 years of related experience, an MS with at least 6 years, or a PhD with at least 3 years.
  • A track record delivering integrated, multi-instrument work cells from concept through deployment.
  • Hands-on experience with liquid handlers such as Hamilton STAR, Agilent Bravo, or Lynx, and robotic arms such as Brooks PreciseFlex.
  • Experience developing interfaces between lab automation and Laboratory Information Management System databases.
  • Proficiency in C#, VB.NET, or Python, and familiarity with XML and JSON.
  • Experience with validation and documentation in regulated environments, such as IVD or LDT.
  • Excellent problem-solving and debugging skills.
  • Ability to work independently and collaboratively with scientific, engineering, operational, and regulatory disciplines.
  • Strong communication, problem-solving, and cross-functional leadership skills.
  • Curiosity, sound judgment, and ability to critically evaluate and responsibly leverage AI-enabled tools in accordance with company policies, ethical standards, and regulatory requirements to improve work efficiency, effectiveness, and quality.
  • Ability to sit for extended periods and lift routine office supplies; work may involve exposure to high noise levels, fumes, and biohazard material in the laboratory environment.
  • A background screening including criminal history is required.

Responsibilities

  • Program, test, troubleshoot, and optimize work cells end to end, from requirements through validation and deployment.
  • Integrate and program liquid handlers, robotic arms using Guidance Development Environment, and peripherals into work cells.
  • Model throughput to identify bottlenecks and guide layout, and own technical risk and failure mode and effects analyses.
  • Evaluate new automation technologies and vendors.
  • Engineer solutions that meet assay performance requirements for precision, timing, temperature, and contamination control.
  • Lead validation strategy, including IQ/OQ/PQ, and set team documentation standards in a regulated environment.
  • Transfer validated work cells into production, including standard operating procedures and training.
  • Partner with assay scientists to translate assay requirements into automated workflows.
  • Set technical direction and coordinate engineers and external integrators.
  • Mentor engineers up to Senior level.
  • Lead design reviews and report milestones and risks to leadership.

Desired Qualifications

  • Experience with next-generation sequencing assays and throughput modeling or simulation.

About the Company

Guardant Health

FDA-approved blood-based cancer diagnostics provider

Guardant Health develops blood-based cancer diagnostics and sells tests to healthcare providers and research institutions. Its flagship product, Guardant360, uses a liquid biopsy to analyze tumor DNA circulating in a patient’s blood to detect mutations and guide treatment decisions for advanced cancer. The company is expanding into early detection and recurrence monitoring, with tests designed to be non-invasive and data-rich for cancer management. Compared with competitors, Guardant Health emphasizes a widely adopted, FDA-approved liquid biopsy platform with broad cancer-type coverage and a focus on providing actionable genomic insights to clinicians. Its goal is to improve cancer outcomes by enabling non-invasive, data-driven decision making across stages of disease and over time.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Palo Alto, CA
Founded
2012

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