4 дня назад
LCMS Scientist (ADME/DMPK)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
LCMS Scientist (ADME/DMPK): Developing and optimizing LC-MS methods and production assays for ADME/DMPK applications in a contract research laboratory with an accent on bioanalytical quantification, method validation, data quality, and mass spectrometer maintenance. Focus on troubleshooting complex analytical workflows, leading small projects, improving processes, and delivering reproducible results under GxP requirements.
Location: St. Charles, Missouri, USA; candidates must be within a commutable distance. Full-time laboratory position working Sunday–Thursday or Saturday–Wednesday, 8:00 PM–5:00 PM.
Company
provides analytical testing, contract research, and laboratory services across food, environmental, pharmaceutical, cosmetic, genomics, and clinical science domains.
What you will do
- Develop liquid chromatography–mass spectrometry methods for ADME/DMPK applications and new assay development.
- Conduct production assays, primarily for ADME Toxicology Services, with potential support for BioMAP, Immunosignaling, Ion Channel, and OncoPanel services.
- Troubleshoot and maintain mass spectrometers and HPLC equipment, including Sciex or Waters instrumentation where applicable.
- Support method validation, process improvements, service-line expansion, equipment development, and data management systems.
- Review data and reports for quality control, maintain reproducible documentation, and communicate project updates to internal and external clients.
- Lead small projects and informal sub-teams, train colleagues and end users, and provide cross-functional support.
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 an equivalent combination of education and experience.
- Direct experience with LC-MS or LC-UV in a CRO or industry laboratory, particularly for ADME/DMPK applications and biological matrices.
- Experience with analytical method development and optimization, bioanalytical validation concepts, liquid handling, automation, solid-phase extraction, HTS, and large-scale screening.
- Experience working within a Quality Management System and following FDA, ICH, GxP, SOP, documentation, and data-quality requirements.
- Experience with small-team leadership, project management, R&D or innovation programs, technical reporting, statistical analysis, and troubleshooting.
- Must be authorized to work in the United States indefinitely without restriction or sponsorship.
Culture & Benefits
- Full-time employment in a laboratory and team-based environment.
- Medical, dental, and vision coverage.
- Life and disability insurance.
- 401(k) plan with company match.
- Paid vacation and holidays.
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