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Celerion

Global CRO for early-phase development

Scientist / Associate Scientist Method Development - Liquid Chromatography–Mass Spectrometry

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeLincoln, NE, USANo salary listedIn-person

About the Job

Requirements

  • A minimum of a Bachelor's degree in Biochemistry, Chemistry, or Biology and 3–5+ years of related industry experience.
  • Strong problem-solving skills.
  • Experience developing LCMS assays in biological samples.
  • Ability to design experiments with multiple variables, including appropriate positive and negative controls.

Responsibilities

  • Develop and qualify highly sensitive, reliable LCMS methods for rapid and accurate analysis of compounds in biological matrices.
  • Consult with clients on method-development and validation needs and establish appropriate bioanalytical assays to meet client needs.
  • Work on projects of diverse scope requiring non-routine analysis and evaluation of scientific data.
  • Work independently and on multiple projects simultaneously in an efficient manner.
  • Interact with validation and production teams to efficiently transfer analytical methods and reagents after development.
  • Troubleshoot assays as needed.
  • Apply design of experiments and other systematic and statistical approaches to method development.
  • Work in a collaborative team environment and communicate professionally.
  • Mentor and provide scientific expertise to the method-development team.

Desired Qualifications

  • Strong knowledge of organic chemistry.
  • Prior experience working in a regulated GLP-compliant environment.
  • Experience developing large-molecule assays by LCMS.
  • Knowledge of laboratory automation, chromatographic and MS-MS software (e.g., Analyst), and LIMS systems (e.g., Watson).
  • Experience with capillary electrophoresis, supercritical fluid chromatography (convergent chromatography), or GC-MS.

About the Company

Celerion

Global CRO for early-phase development

Celerion is a global contract research organization focused on early-phase drug development. It conducts contracted research across clinical trial design, feasibility studies, project management, clinical and medical monitoring, bioanalytical sciences, and regulatory affairs, using High Resolution Mass Spectrometry-based metabolite profiling to inform decisions. Its advantage comes from over 40 years of experience, specialized metabolite profiling, and a global, integrated service model that accelerates development timelines. The goal is to help pharmaceutical and biotech clients bring safe and effective treatments to patients faster through rigorous, high-quality research.

Company size
1,001-5,000
Company stage
Acquired
Total funding
Not listed
Headquarters
Lincoln, NE
Founded
2010

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