Guardant Health

Staff Scientist-LCMS

Guardant Health$150K — $206K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • PhD or MSc in Analytical Chemistry, Biochemistry, or related field
  • 5+ years in targeted LC–MS method development
  • Hands-on experience with PRM (HRMS)
  • In-depth knowledge of quantitative LC–MS workflows in biological matrices

Responsibilities

  • Develop and optimize targeted LC–MS methods for small molecules, lipids, and peptides
  • Design and refine LC gradients for optimal performance
  • Optimize MS/MS parameters including collision energy and resolution
  • Establish and implement quantification strategies
  • Evaluate assay performance metrics like precision and accuracy
  • Assess and mitigate matrix effects
  • Operate and troubleshoot high-resolution MS systems
  • Support method transfer across instruments and sites
  • Integrate workflows with automated sample preparation systems
  • Document methods in compliance with regulatory validation standards

Benefits

  • Hybrid work model with defined in-office collaboration days
  • Flexibility for improved work-life balance
  • Focus on team connectivity and collective scientific advancement
Full Job Description

Key Responsibilities

  • Develop and optimize targeted LC–MS methods (MRM/PRM) for small molecules, lipids, and/or peptides

  • Design and refineLC gradients to achieve optimal separation, sensitivity, and throughput

  • Optimize MS/MS parameters (collision energy, resolution, scan speed, dwell time)

  • Establish and implement quantification strategies (internal standards, calibration curves, QC normalization)

  • Evaluate assay performance: precision, accuracy, linearity, dynamic range, LLOQ/ULOQ

  • Assess and mitigate matrix effects and ion suppression

  • Operate and troubleshoothigh-resolution MS systems (e.g., Orbitrap) and/or triple quadrupole platforms

  • Support method transfer across instruments and sites

  • Integrate workflows with automated sample preparation systems

  • Document methods and support CLIA/FDA-aligned validation and SOP development

Qualifications

  • PhD (or MSc with strong experience) in Analytical Chemistry, Biochemistry, or related field

  • 5+ years of experience in targeted LC–MS method development

  • Hands-on expertise withPRM (HRMS)

  • Strong understanding of quantitative LC–MS workflows in biological matrices

Preferred:

  • Experience in lipidomics, proteomics, or clinical assays

  • Familiarity with regulated environments (CLIA/FDA/ISO)

  • Experience with high-throughput or automated workflows

  • Experience with biological specimens.

  • Experience with high resolution mass spectrometry


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: $150,100 - $206,400 Other US Location(s) Base Pay Range: $127,585 - $175,440 If the role is performed in Colorado, the pay range for this job is: $135,090 - $185,760


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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