Associate Scientist, Raw Materials QC & Wet Chemistry

Insight Global

Florham Park (NJ)

On-site

USD 73,000 - 79,000

Full time

14 days+
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Job summary

Insight Global is seeking an Associate Scientist for QC Raw Materials Testing in Florham Park, NJ. The role focuses on analytical testing to support GMP and non-GMP raw material qualification and release, with responsibilities spanning method evaluation, spec development, and OOS investigations.

The candidate will author GMP documents, coordinate outsourced testing, and work closely with QA, Raw Material Qualification, and Pilot Plant teams to ensure timely material release while upholding GMP

Qualifications

  • BSc in Chemistry or related field required.
  • 1–3 years hands-on wet chemistry experience.
  • GC experience required.
  • FTIR experience with raw materials.
  • Familiar with GMP guidelines and documentation.
  • Experience in pharma/CPG or medical devices preferred.

Responsibilities

  • Perform and oversee analytical testing to support GMP and non-GMP raw material qualification and release activities.
  • Evaluate and implement compendial, vendor, and internal test methods.
  • Develop and maintain raw material specifications.
  • Investigate OOS, atypical, and non-conforming results.
  • Author and review GMP documentation; coordinate outsourced testing with contract laboratories and suppliers.
  • Collaborate cross-functionally with QA, Raw Material Qualification, and Pilot Plant teams to ensure timely material release while maintaining GMP compliance.
  • Emphasize wet chemistry work with strong GC experience.

Skills

Wet chemistry
GMP documentation
OOS investigation

Education

BSc in Chemistry

Tools

GC
FTIR

Job description

Insight Global is seeking an Associate Scientist for QC Raw Materials Testing in Florham Park, NJ. The role focuses on analytical testing to support GMP and non-GMP raw material qualification and release, with responsibilities spanning method evaluation, spec development, and OOS investigations.

The candidate will author GMP documents, coordinate outsourced testing, and work closely with QA, Raw Material Qualification, and Pilot Plant teams to ensure timely material release while upholding GMP

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