Manufacturing Associate, CAR-T

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.

Statement:   Our Manufacturing Associate, Cell Therapy team manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule .   Communication of production deviations and assistance with quality investigations are required , as applicable.   Shift Available:   Quad 4: Wednesday- Saturday (with e/o Wednesday off), Onsite Overnight Shift, 5 p.m. - 5:30 a.m.   * Start and end times are subject to change based on business demands.

Perform set-up and operation of equipment to support production of blood component lots through cell culture, harvest, and cryopreservation.   Support deviation investigations and write ups as needed. Support on time closure of any assigned CAPAs within the designated shift.   Aseptic technique is required for tube most activities: welding, connections, and transfers, at minimum. Aseptic qualification is required .   Weighs and measures in-process materials to ensure proper quantities are added/removed.   Adheres to the production schedule ensuring on-time, internal production logistics .   Records production data and information in a clear, concise, format according to proper GDPs.   Perform all tasks in a manner consistent with site safety policies, quality systems, and GMP requirements.   Works in a team based , cross-functional environment to complete production tasks required by shift schedule.   Motivated, team consciousness individuals are needed to fulfill job requirements.   Become a SME and qualified trainer within a designated function of manufacturing. Supervision will be managed by the shift Supervisor or designated Team Lead.   Maintain on time completion of training assignments to maintain the necessary technical skills and process knowledge.   Performs other tasks as assigned: continuous improvement projects, inspection readiness, right first-time initiatives, etc   Knowledge & Skills:   Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique.   Knowledge of cGMP/FDA regulated industry.   Basic mathematical skills.   General understanding of cGMPs .   Technical writing capability.   Proficient in MS Office applications.   Background to include an understanding of biology, chemistry, medical or clinical practices   Basic Requirements:   A minimum   high   school   diploma   and / or   equivalent is required. An associate   or   bachelor's degree in a related field is preferred.   0–1   year   of   cGMP cell therapy   manufacturing , bioprocessing   manufacturing ,   or   relevant   experience   and   education Working Conditions:   Intermittent walking, standing and sitting to perform job functions; however, ability to stand for extended periods of time may be necessary.   Must be comfortable working with contained human blood components .     Physical dexterity sufficient to use computers and documentation.   Sufficient vision and hearing capability to work in job environment.    Ability to lift 25 pounds.    Must have the ability to work in laboratories and controlled, enclosed, restricted areas.