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Associate Chemist

Job in Edison, Middlesex County, New Jersey, 08818, USA
Listing for: Integrated Resources Inc.
Full Time position
Listed on 2026-02-27
Job specializations:
  • Research/Development
    Medical Technologist & Lab Technician, Research Scientist, Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas:
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

The Chemist will perform a variety of QC testing to assess the strength, identity, and purity of test samples and/or materials. The Chemist will work as part of a team to effectively plan and execute QC analytical testing using established (official and/or in-house) test procedures. The Chemist may perform 90% - 100% of their work at the bench level.

Responsibilities include:

  • Perform sampling, physical, chemical tests, and assays on raw materials, active pharmaceutical ingredients, in-process, finished, and stability products, using various wet chemicals, physical, and instrumental techniques (HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments) according to USP monograph, in-house, or other compendial standards.
  • Plan and maintain inventory of test reagents and solutions, ensuring supplies are ordered as needed.
  • Plan and execute testing within established timelines, including complex testing under supervisory guidance.
  • Record data and results accurately, ensuring clear documentation.
  • Prepare and review Test Procedures, SOPs, and Protocols as assigned.
  • Perform maintenance and calibration of laboratory instruments with supervisory support.
  • Conduct troubleshooting and investigations under supervisor direction.
  • Ensure compliance with all regulatory and in-house requirements, including safety, housekeeping, chemical waste disposal, cGMP, cGLP, and documentation standards.
  • Review analytical documents as required.
  • Qualifications
    • Bachelor's degree in a scientific field, preferably Chemistry
    • 0-2 years of experience in pharmaceuticals
    • Experience in the generic pharmaceutical industry is a plus
    • Knowledge of Good Documentation Practices and familiarity with USP, ICH, FDA guidelines
    • Ability to learn quickly and make decisions effectively
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    Position Requirements
    10+ Years work experience
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