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Scientist I​/II – HPLC Method Development

Job in Exton, Chester County, Pennsylvania, 19341, USA
Listing for: Pharmaron
Full Time position
Listed on 2026-09-04
Job specializations:
  • Research/Development
    Pharmaceutical Science/ Research, Research Scientist, Biotech Research, Drug Discovery
Salary/Wage Range or Industry Benchmark: 55000 - 70000 USD Yearly USD 55000.00 70000.00 YEAR
Job Description & How to Apply Below

Scientist I/II – HPLC Method Development

Position:
Scientist I/II – HPLC Method Development

Salary Range: $55,000-$70,000

Location:

Exton, PA (On-site)

About Pharmaron

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.

We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit

Job Overview:

Join Pharmaron's Bioanalytical Sciences team in Exton, PA, and apply your HPLC method development expertise to challenging drug discovery and development programs.

As a Scientist I/II – HPLC Method Development, you will develop, optimize, troubleshoot, and validate chromatographic methods while supporting the analysis of diverse therapeutic molecules. You'll have the opportunity to work across HPLC and advanced analytical platforms while expanding your exposure to bioanalysis, DMPK, regulated studies, and mass spectrometry applications.

This opportunity is ideal for an early-career analytical scientist with hands-on HPLC method development experience who wants to deepen their expertise in chromatographic method development, complex separations, troubleshooting, and bioanalysis within a global CRO/CDMO environment.

Key Responsibilities

  • Develop, optimize, troubleshoot, and validate HPLC-based analytical and bioanalytical methods supporting drug discovery and development programs.
  • Design and optimize chromatographic conditions, including column selection, mobile phases, gradients, flow rates, and other method parameters to achieve appropriate separation, resolution, sensitivity, and reproducibility.
  • Troubleshoot chromatographic challenges related to peak shape, resolution, selectivity, sensitivity, carryover, retention, and method performance.
  • Perform analytical and bioanalytical sample analysis using HPLC and other available analytical platforms.
  • Design and execute scientifically sound experiments aligned with study requirements, client objectives, and internal quality standards.
  • Process, analyze, interpret, and report chromatographic data while identifying and resolving technical challenges.
  • Support method qualification and validation activities and ensure appropriate scientific documentation of experimental procedures and results.
  • Review and execute study protocols and contribute to protocols, validation reports, technical summaries, study reports, and other scientific documentation.
  • Support developmental and regulated laboratory activities in accordance with applicable procedures and quality requirements.
  • Collaborate with scientists, project teams, management, Business Development, and clients to support successful project execution.
  • Participate in scientific project reviews, technical discussions, troubleshooting activities, and continuous improvement initiatives.
  • Gain exposure to advanced bioanalytical and mass spectrometry applications as experience and project needs develop.

What We're Looking For

  • Bachelor's degree or higher in Analytical Chemistry, Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline.
  • 1–3+ years of relevant analytical or bioanalytical laboratory experience; position level will be determined based on experience and demonstrated technical capabilities.
  • Hands-on experience developing, optimizing, and/or troubleshooting HPLC/LCMS methods.
  • Strong understanding of chromatographic principles, including separation, selectivity, retention, resolution, and method optimization.
  • Experience analyzing and interpreting chromatographic data and troubleshooting analytical challenges.
  • Strong analytical thinking and scientific problem-solving capabilities.
  • Ability to accurately document and communicate experimental procedures, results, and conclusions.
  • Stro…
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