Sr. Data Scientist, Assay Development

DELFI Diagnostics, Inc.

$130K — $170K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree in Applied Math, Statistics, Bioinformatics, Engineering, or a related quantitative field; PhD preferred.
  • 5+ years of scientific or mathematical data analysis experience, with at least 3 years in Python.
  • Strong foundations in probability theory and statistics, including hypothesis testing and variance components.
  • Experience in a regulated diagnostics environment, including executing rigorous studies and analyses.
  • Ability to connect assay chemistry to data behavior to troubleshoot assay performance.

Responsibilities

  • Design and execute analyses supporting assay development and validation for regulated diagnostics.
  • Collaborate with cross-functional teams to interpret results and produce regulatory-compliant documentation.
  • Contribute statistical expertise to control strategy development for quality assurance frameworks.
  • Support operational data science for monitoring production and troubleshoot assay performance issues.
  • Write high-quality Python code following software development best practices.
  • Assist in regulatory submissions with rigorous, documented analysis.

Benefits

  • Flexible time-off policy.
  • 401(k) retirement plan.
  • Comprehensive medical, dental, and vision coverage.
  • Onsite lunch provided 3 days a week.
  • Wellness-related offerings.
Full Job Description
DELFI has 1-2 designated in-office working days each week for employees who live within within 50 miles of Palo Alto, CA

About the Role

The Senior Data Scientist will collaborate with a cross-functional team of laboratory scientists, clinicians, engineers, and other data scientists to develop statistical analysis methods supporting early cancer detection assays. This role spans assay development, analytical validation, and QC and control strategy, contributing to products advancing through verification, validation, and regulatory submission toward clinical use. The ideal candidate brings strong foundations in probability theory and statistics, applied experience in a regulated diagnostics or similarly rigorous data environment, and the ability to translate complex analyses into clear documentation for cross-functional and regulatory audiences.

What You'll Do

  • Design and execute analyses supporting assay development, analytical validation, and QC and control strategy, applying statistical methods appropriate to regulated diagnostic development
  • Collaborate cross-functionally with assay development, lab operations, and software teams to design experiments, interpret results, and produce documentation meeting quality system and regulatory standards.
  • Contribute statistical and data science expertise to control strategy development, including qualification and monitoring frameworks for reagents, instruments, and sample level QC.
  • Provide operational data science support for production and LDT/IVD run monitoring, including troubleshooting assay performance issues, trending QC metrics, and supporting root cause investigations.
  • Produce high quality Python code following best practices established by the software development team.
  • Support regulatory submissions (CLIA/CAP, NYS, FDA as applicable) with rigorous, well documented analysis.


What You'll Bring

Required
  • Master's degree in Applied Math, Statistics, Bioinformatics, Engineering, or a related quantitative field; PhD preferred.
  • Five or more years of practical experience in scientific or mathematical data analysis, with at least three years in Python (numpy, pandas, and similar).
  • Strong foundations in probability theory and statistics, including hypothesis testing, confidence intervals, parameter estimation, and variance components.
  • Experience working in a regulated diagnostics environment (IVD, LDT, or similar), including designing and executing rigorous studies and analyses and documenting them appropriately.
  • Ability to connect assay chemistry to data behavior, applying this understanding to troubleshoot assay performance issues.

Preferred
  • Exposure to NGS based assay development, including familiarity with sequencing data QC and batch level variability.
  • Experience analyzing high dimensional genomic or molecular data.
  • Familiarity with common machine learning techniques and practical experience with implementation and validation.
  • Familiarity with Design of Experiments and related quality methodologies (measurement systems analysis, control charts, Six Sigma/DMAIC).


$130,000 - $170,000 a year

Actual base pay will consider experience, skillset, education, and geography.

This role may be eligible for other forms of compensation, including an annual bonus and a new hire equity grant, subject to the terms of the applicable plans and Company discretion. All employees are also eligible for DELFI's comprehensive and competitive benefits package, including but not limited to: a flexible time-off policy; a 401(k) retirement plan; an extremely competitive medical, dental, and vision coverage; onsite lunch 3 days a week; and other wellness related offerings.

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