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2 дня назад

Research Scientist/Senior Scientist - LC-MS/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

Текст:
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TL;DR
Research Scientist/Senior Scientist - LC-MS/MS (Bioanalytical LC-MS/MS): Developing, validating, transferring, and executing regulated bioanalytical methods for small molecules, peptides, oligonucleotides, ADCs, and monoclonal antibodies with an accent on FDA, EMA, and ICH M10 compliance. Focus on LC-MS/MS troubleshooting, assay documentation, instrument qualification, SOP development, and integrating new capabilities into a CRO laboratory.

Location: Lenexa, Kansas, USA; candidates should be within a commutable distance. Full-time, Monday–Friday, 8:00 a.m.–5:00 p.m., with overtime as needed.

Benefits include medical, dental, and vision coverage; life and disability insurance; a 401(k) with company match; paid vacation; and paid holidays.

Company

hirify.global is an international life sciences company providing analytical testing, laboratory, clinical, pharmaceutical, environmental, food, and agroscience services through a global network of laboratories.

What you will do

  • Develop, optimize, qualify, validate, and transfer LC-MS/MS bioanalytical methods for regulated studies.
  • Perform sample preparation, instrument operation, data analysis, troubleshooting, and routine sample analysis for preclinical and clinical studies.
  • Interpret results and contribute to study reports, validation protocols, technical reports, SOPs, and work instructions.
  • Support onboarding, qualification, and maintenance of LC-MS/MS instruments and laboratory systems.
  • Collaborate with Quality Assurance, Operations, Project Management, and Scientific Leadership.
  • Improve laboratory processes and maintain compliance with GLP, GCP, and company quality requirements.

Requirements

  • BS, MS, or PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Chemistry, or a related discipline.
  • 3–8+ years of relevant bioanalytical laboratory experience, including hands-on LC-MS/MS method development and validation.
  • Working knowledge of FDA, EMA, and ICH M10 bioanalytical method validation requirements.
  • Experience with regulated bioanalytical studies, routine sample analysis, assay validation, sample management, and regulated study workflows.
  • Strong technical writing, documentation, troubleshooting, organizational, and communication skills.
  • Experience in a CRO, pharmaceutical, or biotechnology environment, including laboratory informatics systems such as LIMS and chromatography data systems.

Nice to have

  • Experience with small molecules, peptides, oligonucleotides, antibody-drug conjugates, or monoclonal antibodies.
  • Familiarity with hybrid LC-MS/LBA approaches.
  • Experience with Waters, Sciex, Thermo Fisher, or Shimadzu LC-MS/MS platforms.
  • Experience supporting SOP development and laboratory process implementation.

Culture & Benefits

  • Work in a regulated CRO environment supporting the growth of bioanalytical LC-MS/MS capabilities.
  • Collaborate across scientific, operational, quality, and project management functions.
  • Medical, dental, and vision coverage.
  • Life and disability insurance, 401(k) with company match, paid vacation, and paid holidays.

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