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1 день назад

LCMS Scientist (LC-MS)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
LCMS Scientist (LC-MS): Developing and applying LC-MS methods and production assays for ADME/DMPK contract research services with an accent on bioanalytical quantification, method optimization, and data quality. Focus on troubleshooting mass spectrometers and HPLC systems, validating methods under FDA and ICH guidelines, and leading client projects with minimal supervision.

Location: St. Charles, Missouri, United States; onsite laboratory role within commuting distance. Full-time schedule: Sunday–Thursday or Saturday–Wednesday, 8:00 PM–5:00 AM.

Company

hirify.global is an international life sciences company providing analytical testing, laboratory, pharmaceutical, environmental, food, cosmetic, and contract research services.

What you will do

  • Develop and optimize LC-MS methods for ADME/DMPK applications and new assay development.
  • Conduct production assays and support ADME Toxicology, BioMAP, Immunosignaling, Ion Channel, and OncoPanel services.
  • Troubleshoot and maintain mass spectrometers and HPLC equipment, including Sciex or Waters instrumentation.
  • Support method validation, data and report QC review, data management, and expansion of services and equipment.
  • Manage client projects, communicate project updates, and deliver results with minimal supervision.
  • Maintain laboratory inventory, documentation, SOP compliance, GxP requirements, and data reproducibility.

Requirements

  • B.S. with at least 5 years of relevant laboratory experience, M.S. with at least 3 years, Ph.D. with at least 1 year, or equivalent education and experience.
  • Direct LC-MS or LC-UV experience in a CRO or industry laboratory supporting ADME/DMPK applications.
  • Experience with mass spectrometry-based quantification in biological matrices, analytical method development, and optimization.
  • Knowledge of bioanalytical method validation concepts under FDA and ICH guidelines and experience working in a Quality Management System.
  • Experience with liquid handling, automation, solid-phase extraction, HTS applications, large-scale screening, project management, and small-team leadership.
  • Must be authorized to work indefinitely in the United States without restriction or sponsorship.

Culture & Benefits

  • Collaborative laboratory and cross-functional team environment.
  • Opportunities to train colleagues and contribute to research, development, and new service lines.
  • Medical, dental, and vision coverage.
  • Life and disability insurance, 401(k) with company match, paid vacation, and paid holidays.
  • Commitment to employee health, safety, and equal employment opportunity.

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