QC Data Review Scientist

Seeking a QC Data Review Scientist for our client – a leading contract development and manufacturing organization (CDMO). This is a great opportunity to contribute to the development and commercialization of innovative medicines, from early-stage development through final production.

Type: Direct Hire


  • Identify technical problems, atypical results or methodology malfuctions and assist in the investiagation to correct them.
  • Provide technical support for routine testing activities while conducting analyses of samples, products, and materials.
  • Accurately generate data using validated test methods and SOPs in cGMP environment.
  • Demonstrate technical competence in the use of wet chemical techniques and instrumentation: Infrared Spectroscopy, Ultra Violet/Visible Spectroscopy, Gas Chromatography, High Pressure Liquid Chromatography, Ultra High Pressure Liquid Chromatography, Atomic Absorption Spectroscopy, Dissolution apparatus, Compendial testing (USP, EP, JP).
  • Initiates proper documentation upon discovery of deviations and out of specification results, completes Trackwise write-up for deviations and out of specification results.
  • Performs special projects as assigned including testing, compiling, and trending of data and report generation.
  • Works with vendors for instrument maintenance or upkeep.
  • Understand and execute protocols and provide information to qualify and draft in-house test standards and methods.
  • Revise SOPs and methods as needed.
  • Performs instrument and method related troubleshooting and investigative testing.
  • Responsible for analyzing data, maintaining accurate and detailed written records and notebooks and thorough review of lab notebooks to ensure compliance to test methods and specifications.
  • Maintain training logs to comply with current SOP requirements.


  • Bachelor of science degree in chemistry, biology, or related science required.
  • 2-5 years of experience in a cGMP analytical laboratory
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