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Scientist, Pharmaceutical Science​/ Research, Analytical Chemist

Job in Vernon Hills, Lake County, Illinois, 60061, USA
Listing for: A-Line Staffing Solutions
Full Time position
Listed on 2026-07-03
Job specializations:
  • Science
    Pharmaceutical Science/ Research, Analytical Chemist, Research Scientist
  • Pharmaceutical
    Pharmaceutical Science/ Research, Analytical Chemist
Salary/Wage Range or Industry Benchmark: 35.79 USD Hourly USD 35.79 HOUR
Job Description & How to Apply Below

Scientist I – Analytical Chemistry (HPLC / GC / GMP)

Location: Vernon Hills, IL (Onsite)

Pay: Up to $35.79/hr

Job Summary

We are hiring a Scientist I – Analytical Chemistry to support hands‑on pharmaceutical analytical testing in a GMP / FDA-regulated laboratory environment. This is a bench‑focused role for an Analytical Chemist / QC Analyst type of professional who is comfortable running instrumentation, performing wet chemistry, troubleshooting results, and producing clear, compliant documentation. If you have strong technical writing skills and enjoy solving problems in a fast‑paced lab setting, this is a great opportunity.

What

You’ll Do (Responsibilities)
  • Perform analytical chemistry testing using standard scientific methods and lab procedures
  • Run wet chemistry and instrumental analysis including pH, titration, UV-Vis, GC, and HPLC
  • Troubleshoot analytical issues and document investigations clearly and accurately
  • Maintain compliant GMP documentation and support laboratory quality requirements
  • Interpret written procedures, diagrams, and schedules to execute testing and deliverables
  • Manage multiple assignments while maintaining accuracy, consistency, and scientific rigor
What We’re Looking For (Qualifications)
  • BS/MS in Chemistry, Pharmaceutics, or a related scientific discipline
  • 2–4 years of hands‑on pharmaceutical analytical chemistry experience
  • Strong working knowledge of HPLC and other analytical techniques (GC, UV-Vis, titration, pH)
  • Experience working in an FDA-regulated / GMP environment with strong documentation practices
  • Strong scientific writing, communication, and problem‑solving skills
  • Ability to multitask and keep quality/accuracy high under deadlines
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