Manufacturing Associate, CAR-T - Summit West, NJ

Manufacturing Associate, CAR-T TeamChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.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 with the resources to pursue their goals, both at work and in their personal lives.Our Manufacturing Associate, CAR-T 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: Sunday - Wednesday (with e/o Wednesday off), Onsite Day shift, 5 a.m. - 5:30 pm.Responsibilities:Create inclusive culture that builds relationships with support groupsExecute operations as outlined in Source Governing Documents (including but not limited to: Standard Operating Procedures, Work Instructions, Batch Records, Forms)Executes transactions and process in all electronic systems and adheres to business continuity processesPrioritizes safety of self and othersReports safety events within 24 hoursImmediately escalates any/all issues that may impact compliance or safety of self and/or othersComplete documentation required by Source Governing Documents contemporaneouslyPerform all tasks in a manner consistent with the safety policies, SOPs, quality systems, and GMP requirements including ALCOA+Complete training assignments prior to assigned due date to ensure necessary technical skills and knowledgeTrain for proficiency in process systems and some supporting business systemsExecute the daily unit operations schedule, that includes people, product, and material flow across multiple shiftsWork within a control cleanroom environment and execute aseptic processing procedures (as assigned)Maintain manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirementsContinues to refine and improve manufacturing process technique to improve individual operational timesVerifies training completion prior to performing any GxP tasksAuthor Manufacturing operating procedures that are technically sound, promote effective and efficient operations and comply with cGMP requirements