Manufacturing Associate - CAR-T

Working with UsChallenging. 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. Read more: careers.bms.com/working-with-us.At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.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 requirementsKnowledge & Skills:Knowledge of cGMP/FDA regulated industryBasic mathematical skillsGeneral understanding of cGMPsTechnical writing capabilityProficient in MS Office applicationsInventory control and/or managementBackground to include an understanding of biology, chemistry, medical or clinical practicesBasic Requirements:A minimum high school diploma and/or equivalent is required. An associate or bachelor's degree in a related field is preferred0–1 year of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience and educationWorking Conditions:Must be able to stand/walk for extended periods of timeMust be able to work in a cleanroom environment and perform aseptic processing in ISO 5 biosafety cabinets (as assigned), which require gowning and personal protective equipment (PPE), including by not limited to: safety shoes, safety glasses, aprons, face shields, powered air purifying respirators (PAPR), lab coats, full body gowns, hairnets, gloves, and hearing protectionRequired to carry and/or lift up to 30 pounds / 15 kg, several times a day, while handling production equipment and/or materialsRequired to push and/or pull up to 50 pounds / 25 kg, several times a day, while handling production equipment and/or materialsWork in areas that may have strong magnetsMust be able to work in a BSL2 / ML1 work environment handling human blood componentsWork in areas with exposure to vapor phase liquid nitrogenMust be able to work assigned shift (Day, Evening, Night, Weekends and/or HolidaysBMSCART, #LI-OnsiteIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Compensation Overview:Summit West - NJ - US: $27.83 - $33.72per hour The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on