Bristol-Myers Squibb Company

QC Associate

Location
Devens, MA, US
Posted
Jul 16, 2018
Ref
R1506455
Discipline
Quality, Quality Control
Required Education
Bachelors Degree
Position Type
Full time
Summary:

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

Responsibilities:

  • 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.


Qualifications:
  • 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.