Lead Manufacturing Associate, Cell Therapy Manufacturing

Overview Challenging. 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. Role BMS Cell Therapy Manufacturing seeks a Specialist, Lead Manufacturing Associate Cell Therapy that brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The candidate must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind. We are searching for enthusiastic, and innovative individuals with a good understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy. Shifts Available Day Shift (6am – 6pm). Rotational schedule including holidays and weekends, onsite. Responsibilities Execute operations described in standard operating procedures and batch records. Demonstrates strong practical and theoretical knowledge in their work. Complete documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. Solve complex problems; take new perspectives using existing solutions. Perform tasks in a manner consistent with safety policies, quality systems and GMP requirements. Complete training assignments to ensure the necessary technical skills and knowledge. Set up manufacturing areas and equipment/fixtures. Perform facility and equipment commissioning activities. Collaborate with support groups on recommendations and solving technical problems. Help ensure the shift works effectively in a team-based, cross-functional environment to complete all production tasks required by shift schedule. Collaborate closely with Shift Managers to ensure seamless pass-down and communication of operational status. Support investigations and identify innovative solutions. Support writing manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements. Train others on SOPs, and Work Instructions to successfully complete manufacturing operations. Work with production planning with leadership to execute daily unit operations schedule that includes people, product, and material flow across multiple shifts. Work in a cleanroom environment and perform aseptic processing; maintain manufacturing environmental conditions as required to meet global Health Authority requirements. Knowledge And Skills Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing. Ability to work assigned shift (Day, Night, Weekends and/or Holidays). Ability to work in a cleanroom environment and perform aseptic processing. Comfort being exposed to human blood components. Ability to be in close proximity to strong magnets. Experience in cell therapy manufacturing, including cell washing processes and automated equipment; cell separation techniques and automated equipment; cryopreservation processes and equipment. Experience in aseptic processing in ISO 5 biosafety cabinets and universal precautions for handling human-derived materials in BSL-2 containment areas. Cell expansion using incubators and single-use bioreactors. Basic Requirements 4+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience. Bachelor’s in relevant science or engineering discipline, or equivalent in work experience. Working Conditions Stand and walk for extended periods; operate manufacturing/computer equipment. Lift up to 50 pounds; carry, push, and pull as required. Climb stairs or ladders as needed in production areas. Bend, kneel, and perform overhead work as part of tasks. Repetitive use of arms/hands during setup and processing. Personal protective equipment (PPE) required, including safety shoes, safety glasses, aprons, face shields, lab coats, gowns, hairnets, gloves, and hearing protection. Compensation And Benefits Compensation: Devens - MA - US $40.05 - $48.53 per hour. The starting compensation range is for full-time employees. Additional incentive cash and stock opportunities may be available. Benefits details vary by location. For more, visit careers.bms.com/life-at-bms. Health Coverage including medical, dental, and vision. Wellbeing programs and Employee Assistance Programs. Financial protections including 401(k), disability, life insurance, and other coverages. Work-life And Accessibility Work-life benefits include paid time off (varying by location and role), and other programs. Eligible employees may have additional time off, summer hours, and leave options. Global shutdown periods may apply at year-end. See local policies for details. Uniquely Interesting Work, Life-changing Careers With a vision of “Transforming patients’ lives through science” every BMS employee plays an integral role in work that goes beyond ordinary. We are committed to inclusion, integrity, and accountability while promoting global participation in clinical trials. On-site Protocol BMS occupancy models determine where work is conducted. Site-essential roles require 100% onsite shifts; site-by-design roles may be hybrid with at least 50% onsite. Field-based and remote roles may require travel to meet business needs. Disability And Rights BMS is committed to equal opportunity and provides accommodations during recruitment and employment. For accommodations or questions, contact View email address on click.appcast.io. See careers.bms.com/eeo-accessibility for the Equal Employment Opportunity statement. Candidate Rights BMS will consider qualified applicants with arrest and conviction records, per applicable laws. For California residents, additional information is available at careers.bms.com/california-residents/. Data Protection We will never request payments or sensitive information during the application process. Learn more at careers.bms.com/fraud-protection. All data will be processed in accordance with applicable privacy policies. For questions about the process, contact View email address on click.appcast.io. Job title: Lead Manufacturing Associate, Cell Therapy Manufacturing. #J-18808-Ljbffr Bristol Myers Squibb