QC Associate (Stoughton)

Bristol-Myers Squibb Company in Stoughton, MA

  • Industry: Scientific Research - Health/Medicine/Pharmacology
  • Type: Full Time
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

  • Performs routine testing and data review of stability and batch release samples in a cGMP compliant environment
  • Performs routine assays such as UV-VIS Spectrometry, Appearance testing, pH, Osmolality, moisture content and more assays including various particulate analysis (e.g., Semi-Quant, HIAC).
  • Performs broad range of troubleshooting techniques and leads such within area of expertise.
  • May write and revise SOPs for managerial review and approval.
  • May train less experienced analysts on basic and some more complex test methods.

  • Knowledge of science generally attained through studies resulting in a BS degree, preferably in Chemistry, Molecular Biology, or related discipline.
  • A minimum of 0-2 years of experience in a Biologics QC laboratory or related biopharmaceutical cGLP or cGMP lab.
  • Experience in analytical test methods such as UV/Vis, Osmolality, Moisture analysis and particulate identification is highly preferred.
  • Knowledge of lab software applications (e.g., LIMS, (LES/SmartLab)) preferred.
  • High attention to detail with strong general laboratory and good organizational skills.
  • Demonstrated ability to work independently as well as part of a team, to complete assignments within defined time constraints.
  • Ability to interpret and apply cGMPs, USP, regulatory requirements and industry best practices.
  • Demonstrates problem solving and analytical thinking skills.

Work Environment:
  • QC Associates will work in teams and have continual interaction with members of his/her team as well as other teams throughout the facility in order to exchange information regarding testing completed, in process and planned.
  • All QC Associates will have daily contact with her/his supervisory staff for work assignments, coaching and general management discussions. Incumbents normally receive general instructions on routine work and specific instructions on new assignments.
  • Occasional contact with other line management staff relating to specific project responsibilities may be expected.

Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.
Associated topics: aseptic technique, bacteria, biopharmaceutical, disease, drug discovery, health, immunoassay, injury, medical, vaccine

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