At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.
Position Summary
The Associate position is responsible for performing testing of in-process, final product, and stability samples in accordance with BMS policies, standards, procedures, and Global Regulatory and cGMP requirements to support the Quality Control Analytical department in the Bristol Myers Squibb (BMS) CAR T Manufacturing facility located in Summit, NJ. The candidate may also support data verification and GMP documentation review as needed.
Shift: Wednesday - Saturday, AM (6:30AM-4:30PM)
Duties/Responsibilities
- Perform routine testing of in-process, final product, and stability samples.
- May review GMP documentation and perform data verification.
- Support document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
- May train analysts on general job duties.
- Perform other tasks as assigned.
Job Safety Requirements & Essential Physical Demands
- Ability to lift up to 45 lbs at floor and waist height (commonly
