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2 дня назад

Scientist I Analytical Chemist (LC-MS)

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

Текст:
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TL;DR
Scientist I Analytical Chemist (LC-MS/ADME): Developing and applying analytical chemistry methods for ADME/DMPK contract research assays with an accent on LC-MS method development, biological-matrix quantification, and laboratory quality systems. Focus on validating bioanalytical methods, troubleshooting mass spectrometers and HPLC units, and delivering client projects with accurate, reproducible data.

Location: St. Charles, Missouri, United States. On-site laboratory role requiring a commutable distance. Full-time schedule: Sunday–Thursday or Saturday–Wednesday, 8:00 PM–5:00 AM.

Company

hirify.global provides analytical testing and contract research services across food, environmental, pharmaceutical, cosmetic, genomics, and life sciences markets.

What you will do

  • Conduct production assays primarily for ADME Toxicology Services and support other discovery service areas as needed.
  • Develop and optimize LC-MS methods for ADME/DMPK applications and new assay development.
  • Troubleshoot and maintain mass spectrometers and HPLC equipment while managing laboratory reagents, buffers, and inventory.
  • Support method validation, data and report quality control, data management systems, and service-line expansion.
  • Lead client projects with minimal supervision, communicate project updates, and provide cross-functional support.
  • Train colleagues and external users while contributing to research and development objectives.

Requirements

  • Bachelor’s degree with at least 5 years of relevant laboratory experience, master’s degree 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 ADME/DMPK applications within a CRO or industry laboratory.
  • Experience with analytical method development and optimization, mass spectrometry-based quantification in biological matrices, and quality management systems.
  • Knowledge of bioanalytical method validation under FDA and ICH guidelines, plus experience with liquid handling, automation, SPE, HTS, and large-scale screening.
  • Experience leading small teams, managing projects, and delivering R&D or innovation programs.
  • Must be authorized to work indefinitely in the United States without restriction or sponsorship.

Nice to have

  • Experience with Sciex or Waters instrumentation.
  • Interest in drug discovery and advancing human health.

Culture & Benefits

  • Collaborative laboratory environment with opportunities to support cross-functional teams.
  • Comprehensive medical, dental, and vision coverage.
  • Life and disability insurance.
  • 401(k) plan with company match.
  • Paid vacation and holidays.

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