Bristol-Myers Squibb
Manager, Cell Therapy Manufacturing in Devens, MA
Bristol-Myers Squibb, Devens, Massachusetts, us, 01434
Manager Of Cell Therapy Manufacturing
Working with us is challenging, meaningful, and life-changing. At Bristol Myers Squibb, 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. Bristol Myers Squibb is 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. BMS is seeking a Manager of Cell Therapy Manufacturing for a manufacturing facility in Devens, MA. The Manager will support the start-up and commercial licensure of the Cell Therapy facility. This manager will be responsible for shifts that cover 24/7 cell therapy operations and will oversee manufacturing associates. Shifts Available: Day Shift: 6am 6pm, rotating schedule including holidays and weekends Night Shift: 6pm 6am, rotating schedule including holidays and weekends Responsibilities: Manage the creation, implementation, and compliance for all documentation, procedures, and policies Operate within the requirements of a validated manufacturing systems, plan, assign and oversee daily operational activities associated with assigned areas of responsibility. Maintain operating and storage areas that are compliant, efficient, effective, and safe. Identify strategic and operational issues to prevent deviations and maintain a compliant environment. Lead and manage the development of corrective and preventative actions, deviation responses, and investigations. Manage implementation and maintenance of appropriate training curricula Create an environment of teamwork, open communication, and a sense of urgency. Foster a culture of safety and compliance that embraces safety in the work environment and the safety of the patients by compliance with company procedures and policies, and cGMP requirements. Efficiently coordinate, communicate, and provide Operations project information and activities status to Planning, Manufacturing, Quality Assurance/Operations, Global Supply, and other associated functions in a timely manner in accordance with schedules and defined implementation timelines. Oversee operators on a daily basis as they: Perform unit operations and support operations described in standard operating procedures and batch records in a safe and GMP compliant manner. Complete documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. Maintain training assignments to ensure the necessary technical skills and knowledge. Assist in the setup of manufacturing areas and equipment/fixtures and perform facility and equipment commissioning, qualification, and validation activities. Writing manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements. Hire, mentor, and develop exceptional people: Conduct performance reviews and identify opportunities for career growth for manufacturing associates. This position will require shift work, including holidays and weekends. This position will require you to work in a clean room environment, with exposure to human blood components and in close proximity to strong magnets. Knowledge and Skills: Advanced ability to accurately and completely understand, follow, interpret, and apply global regulatory and cGMP requirements. Demonstrated advanced technical writing skills. Advanced strategic thinking and problem-solving ability/mentality, technically adept and logical. Ability to work independently in a fast-paced team environment, meet deadlines, and prioritize work from multiple projects. Advanced ability to communicate and collaborate effectively with peers, senior management, and cross-functional peers about task status, roadblocks, and needs, locally and globally. Advanced mentoring, coaching, influencing, negotiating, and personnel interaction skills. Basic Requirements: Bachelors in relevant science or engineering discipline, or equivalent in work experience. 5+ years of experience in cGMP biologics cell culture manufacturing Experience in the following is highly preferred: Cell therapy manufacturing 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, cell washing processes, cell separation techniques and cryopreservation processes and equipment. The starting compensation for this job is a range from $110,810-$134,300, plus incentive cash and stock opportunities (based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental, and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources. Other perks like tuition reimbursement, and a recognition program.
Working with us is challenging, meaningful, and life-changing. At Bristol Myers Squibb, 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. Bristol Myers Squibb is 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. BMS is seeking a Manager of Cell Therapy Manufacturing for a manufacturing facility in Devens, MA. The Manager will support the start-up and commercial licensure of the Cell Therapy facility. This manager will be responsible for shifts that cover 24/7 cell therapy operations and will oversee manufacturing associates. Shifts Available: Day Shift: 6am 6pm, rotating schedule including holidays and weekends Night Shift: 6pm 6am, rotating schedule including holidays and weekends Responsibilities: Manage the creation, implementation, and compliance for all documentation, procedures, and policies Operate within the requirements of a validated manufacturing systems, plan, assign and oversee daily operational activities associated with assigned areas of responsibility. Maintain operating and storage areas that are compliant, efficient, effective, and safe. Identify strategic and operational issues to prevent deviations and maintain a compliant environment. Lead and manage the development of corrective and preventative actions, deviation responses, and investigations. Manage implementation and maintenance of appropriate training curricula Create an environment of teamwork, open communication, and a sense of urgency. Foster a culture of safety and compliance that embraces safety in the work environment and the safety of the patients by compliance with company procedures and policies, and cGMP requirements. Efficiently coordinate, communicate, and provide Operations project information and activities status to Planning, Manufacturing, Quality Assurance/Operations, Global Supply, and other associated functions in a timely manner in accordance with schedules and defined implementation timelines. Oversee operators on a daily basis as they: Perform unit operations and support operations described in standard operating procedures and batch records in a safe and GMP compliant manner. Complete documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. Maintain training assignments to ensure the necessary technical skills and knowledge. Assist in the setup of manufacturing areas and equipment/fixtures and perform facility and equipment commissioning, qualification, and validation activities. Writing manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements. Hire, mentor, and develop exceptional people: Conduct performance reviews and identify opportunities for career growth for manufacturing associates. This position will require shift work, including holidays and weekends. This position will require you to work in a clean room environment, with exposure to human blood components and in close proximity to strong magnets. Knowledge and Skills: Advanced ability to accurately and completely understand, follow, interpret, and apply global regulatory and cGMP requirements. Demonstrated advanced technical writing skills. Advanced strategic thinking and problem-solving ability/mentality, technically adept and logical. Ability to work independently in a fast-paced team environment, meet deadlines, and prioritize work from multiple projects. Advanced ability to communicate and collaborate effectively with peers, senior management, and cross-functional peers about task status, roadblocks, and needs, locally and globally. Advanced mentoring, coaching, influencing, negotiating, and personnel interaction skills. Basic Requirements: Bachelors in relevant science or engineering discipline, or equivalent in work experience. 5+ years of experience in cGMP biologics cell culture manufacturing Experience in the following is highly preferred: Cell therapy manufacturing 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, cell washing processes, cell separation techniques and cryopreservation processes and equipment. The starting compensation for this job is a range from $110,810-$134,300, plus incentive cash and stock opportunities (based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental, and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources. Other perks like tuition reimbursement, and a recognition program.