glpmethod validationsample preparationlimsmass spectrometryuplcbioanalysistriple quadrupolelcms ms
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Очень мало
$41к-108к/год
$99к$120кмедиана$140к
По похожим ролям (50) ~ $120к/год
68
Средняя вакансия
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Профессиональная роль в мировом лидере клинических исследований с очень четким описанием задач, но зарплата ниже рыночного медианного значения, а разброс вилки слишком велик.
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Низкая зарплатаСовременный стекПерспективный доменЧеткие задачи
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Scientists (LCMS-MS Bioanalysis & Method Validation) (LC–MS bioanalysis): Designing and executing qualitative and quantitative experiments for large- and small-molecule workflows in a regulated laboratory environment with an accent on method validation, sample preparation, and high-quality data generation. Focus on operating and troubleshooting LC–MS and UPLC instrumentation, interpreting chromatographic data, and preparing GLP-compliant documentation and study deliverables.
Location: Ithaca, New York, United States of America; onsite laboratory role
Base pay: $41,400–$108,000 annually
Company
IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
Design, set up, and execute qualitative and quantitative experiments supporting LC–MS bioanalysis, method validation, and downstream sample analysis.
Prepare, extract, and process samples using protein precipitation, solid-phase extraction, and immunocapture techniques.
Operate, calibrate, tune, optimize, maintain, and troubleshoot Triple Quadrupole mass spectrometers and UPLC systems according to SOPs.
Review and interpret chromatographic and mass spectrometry data, identify abnormalities, and initiate troubleshooting studies.
Prepare protocols, technical summaries, reports, GLP-compliant laboratory notebook entries, and data packages.
Collaborate with Project Management and cross-functional stakeholders to plan work, communicate progress, and meet study objectives.
Requirements
Bachelor’s degree in applied or laboratory sciences or a relevant scientific discipline with direct laboratory coursework, or an equivalent combination of education, training, and experience.
Hands-on experience with LC–MS workflows, including Triple Quadrupole and/or high-resolution mass spectrometers, UPLC systems, calibration, tuning, and data interpretation.
Knowledge of sample handling and preparation techniques, including protein precipitation, SPE, and immunocapture.
Familiarity with GLP documentation standards and ability to produce accurate, compliant data and documentation within deadlines.
Ability to troubleshoot complex experiments and laboratory equipment, present findings clearly, and determine when to escalate issues.
Effective communication and interpersonal skills for collaboration with project teams and cross-functional stakeholders.
Nice to have
Experience preparing data for LIMS, such as Watson.
Experience supporting the evaluation of new laboratory technologies and process improvements.
Culture & Benefits
Inclusive collaboration focused on advancing healthcare research and development.
Benefits and resources supporting employees’ physical, mental, emotional, financial, and social well-being.
Health and welfare benefits may be provided in addition to base pay.
Potential incentive plans, bonuses, and other compensation may be available depending on the position.
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