Senior Scientist, Ivd Product Development

Natera

San Carlos, CA, United States
Base: $138,100 - $172,600 usd; bonus/equity: annua...
On-site
Automated high-throughput ngs assay development
Ivd product development and design controls
Clia laboratory protocol validation
Natera is seeking a Senior Scientist for their Early Cancer Detection product development team, focusing on reagent and process optimization for IVD products. The ideal candidate will have extensive experience in assay development, particularly in NGS-based diagnostics, and will work collaboratively in a fast-paced environment

Job Summary

  • Natera is a global leader in cell-free DNA testing dedicated to developing oncology product portfolios.
  • The Senior Scientist will design, develop, and validate automated high-throughput NGS assays for commercial CLIA laboratories.
  • This position offers competitive compensation including annual performance incentives, long-term equity awards, and comprehensive health benefits.

Matching Summary

Match Score: 85

Natera is seeking a Senior Scientist for their Early Cancer Detection product development team, focusing on reagent and process optimization for IVD products. The ideal candidate will have extensive experience in assay development, particularly in NGS-based diagnostics, and will work collaboratively in a fast-paced environment.

Salary

Base: $138,100 - $172,600 USD; Bonus/Equity: Annual performance incentive bonus and long-term equity awards; Benefits: Comprehensive medical, dental, vision, 401(k) match, and paid time off

Skills & Requirements

Must-have

  • Automated high-throughput NGS assay development
  • IVD product development and design controls
  • CLIA laboratory protocol validation
  • Reagent and process optimization
  • Liquid handler robot programming

Nice-to-have

  • Python or R coding skills
  • Mentoring junior employees
  • Continuous improvement of workflows
  • Cross-functional collaboration
  • Fast-paced environment adaptability

Key Requirements

  • BA/BS with 8+ years experience
  • MS with 5+ years experience
  • PhD with 3+ years experience
  • Experience with FDA submission protocols
  • Track record of CLIA lab automation

Work Rights

Not specified

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