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2 дня назад

LC-MS/MS Sr. Scientist (ADME/DMPK)

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

Текст:
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TL;DR
LC-MS/MS Sr. Scientist (ADME/DMPK): Developing and applying LC-MS methods for ADME/DMPK assays and bioanalytical research services with an accent on analytical method development, mass spectrometry-based quantification, and data quality. Focus on troubleshooting laboratory instrumentation, validating methods, leading client projects, and delivering reproducible results in a GxP environment.

Location: St. Charles, Missouri, USA; candidates must be within a commutable distance. Full-time laboratory role with Sunday–Thursday or Saturday–Wednesday schedules, 8:00 AM–5:00 PM.

Company

hirify.global provides analytical testing, contract research, pharmaceutical, environmental, food, and life sciences services through a global laboratory network.

What you will do

  • Develop LC-MS methods for ADME/DMPK applications and new assay development.
  • Conduct production assays across ADME Toxicology Services and support additional discovery service areas as needed.
  • Troubleshoot and maintain mass spectrometers and HPLC equipment, including Sciex or Waters instruments.
  • Manage laboratory inventories, reagents, buffers, equipment, and data management systems.
  • Review and QC data and reports while maintaining high data quality, reproducibility, and accurate documentation.
  • Lead client projects, support validation and R&D programs, train colleagues, and communicate project updates to internal and external clients.

Requirements

  • Bachelor’s degree plus at least 5 years of industry laboratory experience with LC-MS/MS; or a master’s degree plus 3 years; or a Ph.D. plus 1 year.
  • Direct LC-MS or LC-UV experience in ADME/DMPK applications within a contract research organization or industry laboratory.
  • Expertise in mass spectrometry-based quantification for ADME/DMPK applications in biological matrices and analytical method development.
  • Experience with quality management systems, bioanalytical method validation concepts, FDA and ICH guidelines, liquid handling, automation, SPE, HTS, and large-scale screening.
  • Experience leading small teams, managing projects, and delivering R&D or innovation programs.
  • Authorization to work indefinitely in the United States without restriction or sponsorship is required.

Culture & Benefits

  • Full-time employment with medical, dental, and vision coverage.
  • Life and disability insurance.
  • 401(k) plan with company match.
  • Paid vacation and holidays.
  • Work in a collaborative laboratory environment focused on drug discovery, quality, safety, and advancing human health.

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