Bristol-Myers Squibb Company

QC Associate

Devens, MA, US
Jul 16, 2018
Quality, Quality Control
Required Education
Bachelors Degree
Position Type
Full time

To perform QC analytical testing in support of biologics bulk drug substance manufacturing using defined methods in a cGMP compliant laboratory. Assures test results are accurately recorded and abnormal data or equipment/instrument malfunctions are promptly reported to his/her supervisor


  • Performs routine testing and data review of batch release and stability samples of Bulk Drug Substance in a cGMP compliant environment.
  • Performs routine assays such as UV-VIS Spectrometry, SDS Page and various HPLC methodologies, (e.g. SEC and reverse phase).
  • Performs sample management including: sample receipt, sample tracking, aliquots preparation, and sample distribution.
  • Aids in troubleshooting equipment and methods.

  • Knowledge of science generally attained through studies resulting in a B.S. in chemical sciences, a related discipline, or its equivalent is required.
  • Knowledge of laboratory techniques such as pH, volumetric measurement and basic laboratory safety practices.
  • Some understanding of regulatory standards.
  • Some relevant experience in a biologics QC lab preferred.