Bristol Myers Squibb QC Associate in Devens, Massachusetts
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.
We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.
Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.