Clinical Diagnostics Lab Specialist - MS/LC-MS & ELISA

Biodesix

De Soto (KS)

On-site

USD 84,000 - 90,000

Full time

3 days ago
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Benefits offered by this job

Health coverage
Disability & Life Insurance
Vacation 120 hours
Sick leave 72 hours
11 holidays + 3 floating holidays
Employee Assistance Program
Voluntary Benefits
Employee recognition program

Job summary

Biodesix seeks a Product Technical Specialist to support late-stage product concepts within a regulated Kansas laboratory. The role focuses on developing and optimizing chromatography, mass spectrometry, and ELISA methods to meet clinical and analytic requirements for diagnostic tests.

You will perform maintenance, troubleshooting, and ensure documentation aligns with GDP and regulatory standards. You will work with CAP/CLIA and NYS CLEP requires, collaborating with cross-functional teams across

Qualifications

  • Master’s or doctoral degree with relevant experience in clinical laboratory science.
  • Experience with ELISA, HPLC and/or LC-MS methods in a regulated lab environment.
  • Strong documentation and GMP/GLP familiarity.

Responsibilities

  • Develop and optimize chromatography, mass spectrometry, and ELISA methods for clinical/analytic requirements.
  • Perform preventative maintenance and troubleshoot chromatography, MS and ELISA instrumentation.
  • Maintain thorough documentation and adherence to GDP and QMS.
  • Collaborate across CAP/CLIA, NYS CLEP and cross-functional teams on late-stage product development.

Skills

ELISA
HPLC
LC-MS
Data analysis
Documentation
Communication
Lab safety

Education

MS/PhD in chemical/biological sciences

Tools

ELISA Instrumentation
HPLC Systems
LC-MS Instruments

Job description

Biodesix seeks a Product Technical Specialist to support late-stage product concepts within a regulated Kansas laboratory. The role focuses on developing and optimizing chromatography, mass spectrometry, and ELISA methods to meet clinical and analytic requirements for diagnostic tests.

You will perform maintenance, troubleshooting, and ensure documentation aligns with GDP and regulatory standards. You will work with CAP/CLIA and NYS CLEP requires, collaborating with cross-functional teams across

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