Guardant Health

Scientist II- Assay Development

Guardant Health$122K — $168K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD in molecular biology, biomedical sciences, or related field with 2+ years of relevant industry experience.
  • Background in research, development, or optimization of Next-Generation Sequencing (NGS) technologies, especially with cell-free nucleic acids.
  • Proficient in data analysis using Python, R, or JMP; experience with large datasets is essential.
  • Detail-oriented with proven ability to organize and document scientific findings effectively.
  • Collaborative team player, adaptable to change, and enjoys a fast-paced environment.
  • Strong curiosity and motivation to explore and learn new technologies.
  • A sense of humor is essential for cultural fit.

Responsibilities

  • Evaluate, optimize, and implement advanced research and technologies in molecular oncology.
  • Identify and propose solutions for improving existing assays.
  • Collaborate effectively with cross-functional teams to meet product objectives.
  • Deliver results with a strong commitment in a fast-paced environment.
  • Document technical evaluations and create standard operating procedures (SOPs).
  • Present findings, data, and proposals in various settings.

Benefits

  • Hybrid work model allowing flexibility between in-office collaboration and remote work.
  • Structured in-office days to enhance team connectivity and focused work time.
  • Commitment to reasonable accommodations for candidates with disabilities.
  • Supportive work environment promoting work-life balance.
Full Job Description

Profile Summary:

As a Scientist II in the Technology Development Team, you will work collaboratively with team members and interface cross-functionally with bioinformatics, process engineering, system engineering, and other assay development teams. You will be hands-on in the lab to evaluate and optimize new assays related to liquid biopsy sequencing technologies for detecting, treating, and monitoring all cancer types. You will play a critical role in the design and implementation of our advanced cancer diagnostics product as well as future product oerings.

In the Assay Development team, you will collaborate cross-functionally with members from research, bioinformatics, process engineering, operations, and software. You will lead and analyze studies to further the development of automated molecular assays for the early detection, treatment and monitoring of all cancer types.

Essential Duties and Responsibilities:

  • Assess, optimize, and implement cutting-edge research and technologies in molecular oncology and diagnostics to improve assay performance

  • Identify areas for improvement in current assays and propose and implement solutions

  • Collaborate within Technology Development and cross-functionally with bioinformatics as well as other cross-functional teams to facilitate eective execution of product goals

  • Be highly committed to deliver results in a fast-paced and rapidly growing organization Document technical evaluations and provide SOPs as needed

  • Present data, proposals, and progress in various forums

Qualications:

  • PhD degree in molecular biology, biomedical sciences, or related eld with 2+ years of industry work

  • Experience in research, development and/or optimization of NGS technologies with strong preference for experience with cell-free nucleic acids

  • Strong data analysis skills with experience with Python, R, or JMP and the experience in handling large datasets

  • Detail orientated with demonstrated ability to organize, document and communicate scientic data

  • Committed team player; enjoys working both independently and collaboratively in a fast-paced environment and able to adapt to change, demonstrating flexibility and the ability to learn and apply new technologies

  • Strong underlying curiosity and drive


AI & Digital Fluency

  • Demonstrate curiosity, sound judgment, and the ability to critically evaluate and responsibly leverage AI-enabled tools in accordance with company policies, ethical standards, and regulatory requirements to improve the efficiency, effectiveness, and quality of work.


Hybrid Work Model:This section is applicable to onsite employees who are eligible for hybrid work location as specified by management and related policies.  Guardant has defined days for in-person/onsite collaboration and work-from-home days for individual-focused time. All U.S. employees who live within 50 miles of a Guardant facility will be required to be onsite on Mondays, Tuesdays, and Thursdays. We have found aligning our scheduled in-office days allows our teams to do the best work and creates the focused thinking time our innovative work requires. At Guardant, our work model has created flexibility for better work-life balance while keeping teams connected to advance our science for our patients.

The annualized base salary ranges for the primary location and any additional locations are listed below. This range does not include benefits or, if applicable, bonus, commission, or equity. Each candidates compensation offer will be based on multiple factors including, but not limited to, geography, experience, education, job-related skills, job duties, and business need. Primary Location: Palo Alto, CA Primary Location Base Pay Range: $122,600 - $168,600 Other US Location(s) Base Pay Range: $104,210 - $143,310 If the role is performed in Colorado, the pay range for this job is: $110,340 - $151,740


Employee may be required to lift routine office supplies and use office equipment.Majority of the work is performed in a desk/office environment; however, there may be exposure to high noise levels, fumes, and biohazard material in the laboratory environment.Ability to sit for extended periods of time.

About Guardant Health

Guardant Health, Inc. is a precision oncology company that develops and commercializes blood tests for early cancer detection and treatment. The company's flagship product, Guardant360, is a liquid biopsy test that analyzes cancer-related genes in the blood to help doctors make more informed treatment decisions. Guardant Health was founded in 2012 and is headquartered in Redwood City, California. The company has partnerships with several pharmaceutical companies and has received FDA approval for several of its products.
Learn more about Guardant Health
Size
1,373 employees
Market Cap
$2.8 billion
Industry
Net Income
-$253.7 million
Founded
2012
5 Year Trend
+71.4%
Revenue
$286.7 million
NASDAQ

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