Bioanalytical LC-MS/MS Chemist — Method Development

LUKOS LLC

Atlanta (GA)

On-site

USD 90,000 - 120,000

Full time

14 days+
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Job summary

Lukos seeks a Bioanalytical Chemist to advance clinical and translational research using LC-MS/MS method development and biological specimen processing under BSL-2 protocols. You will quantitate small-molecule drugs across diverse matrices and ensure data integrity and audit readiness.

Ideal candidates hold a BS in Chemistry/Biochemistry with 5–7+ years of hands-on experience; a Master's is preferred. Strong calibration, QA/QC, and compliance with QMML/GLP are essential.

Qualifications

  • Hands-on experience developing and validating small-molecule LC-MS/MS assays per FDA/EMA bioanalytical guidelines.
  • Experience with sample prep (SPE, LLE, protein precipitation) and complex matrix handling.
  • Familiarity with ISO 17025, CLIA, CAP, or GLP standards and QMS/QMML practices.
  • Ability to maintain logbooks, IQ/OQ/PQ, and GDP/LIMS/ELN for audit readiness.

Responsibilities

  • Process biological and other potentially hazardous specimens for chemical drug analysis.
  • Develop and validate new analytical methods to measure small molecular weight compounds in biological specimens.
  • Collect, process, aliquot and store biological specimens. Analyze antiretroviral and antimicrobial drug distribution in specimens.
  • Calibrate and maintain LC-MS instruments and analytical balances; record calibration for QMS/QMML.
  • Perform serologic and molecular assays pertinent to program studies.
  • Maintain experiment records, analyze data, and prepare data/results for reports.

Skills

LC-MS/MS
Bioanalysis
Method development
BSL-2 safety
SPE/LLE
qPCR
GLP/QA standards
GDP/LIMS/ELN

Education

Bachelor's in Chemistry/Biochemistry
Master's degree preferred

Job description

Lukos seeks a Bioanalytical Chemist to advance clinical and translational research using LC-MS/MS method development and biological specimen processing under BSL-2 protocols. You will quantitate small-molecule drugs across diverse matrices and ensure data integrity and audit readiness.

Ideal candidates hold a BS in Chemistry/Biochemistry with 5–7+ years of hands-on experience; a Master's is preferred. Strong calibration, QA/QC, and compliance with QMML/GLP are essential.

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