QC Associate Scientist


Concord, OH


QC Associate Scientist

Essential Responsibilities

  • Perform routine HPLC and GC analysis in a GMP analytical laboratory
  • May also perform FTIR, KF, DSC, TGA, IC, NMR, and polarimetry
  • Coordinate raw material testing in a materials management system
  • Conduct inspections of manufacturing supplies
  • Experience with sampling raw materials and intermediates
  • Coordinate the timely and compliant generation of data to support client projects
  • Review data for technical content and good record keeping practices
  • Other duties as assigned


Educational Qualifications

  • BS to PhD in chemistry with 2+ years related pharmaceutical analytical laboratory experience or equivalent combination of education and experience is required.
  • Relevant experience in good laboratory/manufacturing practices (GLP/cGMP), laboratory quality control or stability, and interaction with quality assurance is required.

Specific Skills and Requirements

  • Experience with HPLC and GC analysis
  • Experience with standard lab equipment (balances, pipettes, pH meter, etc.)
  • Be proficient in Microsoft Excel and Word
  • Must have basic chemical knowledge and be able to handle materials safely.
  • Must be able to communicate effectively with manufacturing and quality personnel.
  • Must be able to effectively multitask.
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