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Chemist II

Job in Northridge, Los Angeles County, California, 91325, USA
Listing for: Integrated Resources, Inc
Full Time position
Listed on 2026-08-01
Job specializations:
  • Science
    Research Scientist, Analytical Chemist, Clinical Research, Data Scientist
  • Research/Development
    Research Scientist, Clinical Research, Data Scientist
Job Description & How to Apply Below
Location: Northridge

Title:
Chemist II

Location:
Northridge, CA 91325

Duration: 12 Months+ Possible Extension

Description

  • We are seeking a Chemist II with hands-on experience in analytical techniques including FTIR, ICP-MS, LC-UV/LC-MS, and GC-FID/MS.
  • The candidate will perform qualitative and quantitative analyses on a variety of sample types to support new product development.
  • Responsibilities also include assisting in method development, maintaining laboratory instrumentation, and ensuring compliance with
  • laboratory protocols. The Chemist II will contribute to protocol and report writing, data interpretation, and general laboratory support activities.
  • Performs routine and non-routine qualitative and quantitative analyses of raw materials, in-process samples, and finished products using techniques such as FTIR, ICP-MS, LC-UV/LC-MS, GC-FID/MS, and others.
  • Develops and improves analytical methods; validates methods in compliance with regulatory standards.
  • Supports product development activities by executing analytical testing, compatibility studies, and development plans.
  • Applies a strong understanding of underlying chemistry to method development, data interpretation, and troubleshooting analytical challenges.
  • Conducts exploratory research to produce new knowledge and potential products; conceives, organizes, promotes, and executes ideas and plans to increase chemistry's role in and contribution to the discovery and chemical approaches to meet exploratory objectives in product discovery.
  • Develops research proposals to provide a technically and economically sound basis for developing and evaluating new or improved products, synthetic methods, processes, and analytical and physical testing techniques.
  • Recommends utilization of the results or changes in the Product of work or termination of projects.
  • Prepares and reviews technical documents including protocols, reports, and data sheets for analytical parameters.
  • Conducts analytical work in compliance with cGMP, regulatory standards, and safe laboratory practices; documents any variances appropriately.
  • Frequently applies regulatory standards to drug and device testing.

Must Have Requirements:

  • Strong analytical chemistry background, method development/validation, cGMP knowledge, product development support, technical documentation, troubleshooting, and regulatory testing experience.

Technical Skills:

  • Microsoft office, LIMS, Empower software
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