Bristol-Myers Squibb
NIGHT SHIFT: Senior Manufacturing Associate, Cell Therapy in Devens, MA
Bristol-Myers Squibb, Harvard, Massachusetts, us, 01451
Working with Us
Challenging. Meaningful. Life-changing. Bristol Myers Squibb offers work that transforms lives, with opportunities to grow and thrive alongside high-achieving teams. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of benefits, services and programs that support employees in pursuing their goals at work and in their personal lives. Read more about working with us on careers.bms.com. At
Bristol Myers Squibb
we are reimagining the future of cell therapy with a bold ambition and a best-in-class team, leading the way to unlock the full promise of cell therapy and put more patients on the path to a cure. If you are ready to challenge yourself and accelerate your career, there’s no better place than here at BMS with our Cell Therapy team. BMS Cell Therapy Manufacturing is seeking a
Senior Manufacturing Associate, Cell Therapy
to bring enthusiasm, intellectual curiosity, scientific rigor, and a drive to advance novel programs. The candidate should be goal-oriented, flexible, and able to work efficiently with safety and quality in mind. We are seeking enthusiastic and innovative individuals with a solid understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy. Shifts Available:
6pm - 6am, rotating shift including holidays and weekends, onsite. Responsibilities: Execute operations described in standard operating procedures and batch records. Demonstrate strong practical and theoretical knowledge in work. Complete documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. Solve simple problems; apply existing solutions from new perspectives. Perform tasks in a manner consistent with safety policies, quality systems, and GMP requirements. Complete training assignments to ensure necessary technical skills and knowledge. Train others on SOPs and Work Instructions to successfully complete manufacturing operations. Support investigations. Identify innovative solutions. Assist in setting up manufacturing areas and equipment/fixtures; perform facility and equipment commissioning activities. Write 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 complete manufacturing operations. Coordinate with production planning to execute daily unit operations schedules across multiple shifts. Work in a cleanroom environment and perform aseptic processing; maintain environmental conditions to meet health authority requirements. Knowledge and Skills: Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing. Ability to work assigned shifts (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. Preferred: aseptic processing in ISO 5 biosafety cabinets and universal precautions for handling human-derived materials in BSL-2 containment areas. Experience with cell expansion using incubators and single-use bioreactors. Basic Requirements: High school diploma and 3+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing, or relevant experience. Bachelor’s degree in a relevant science or engineering discipline with relevant experience strongly preferred. Working Conditions: Stand and walk for several hours at a time while operating manufacturing/computer equipment. Carry, lift, push, and/or pull up to 50 pounds several times a day. Climb steps or ladders several times a day. Bend and kneel several times a day. Overhead work and repetitive movements required several times a day. Wear PPE and clean room garments daily (safety shoes, safety glasses, gowns, hairnets, gloves, etc.). BMSCART #LI-ONSITE GPS_2025 If 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:
Devens - MA - US: $32.00 - $38.77 per hour. The starting compensation range for this role is listed above for a full-time employee basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account factors such as required skills, location, work schedule, and experience. Final compensation will be determined 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 careers.bms.com/life-at-bms. Benefit offerings are subject to the terms and conditions of the applicable plans and may include medical, dental, vision, wellbeing programs, 401(k), disability, life insurance, and other programs. Some programs provide paid holidays, vacation, volunteer days, sick time, and various leave options. Other perks include tuition reimbursement and a recognition program. Uniquely Interesting Work, Life-changing Careers With a vision like Transforming patients’ lives through science, each BMS employee contributes to work that goes beyond ordinary. We value passion, innovation, urgency, accountability, inclusion, and integrity. On-site Protocol BMS uses an occupancy structure to determine where an employee conducts their work. Roles may be site-essential (100% onsite), site-by-design (hybrid with at least 50% onsite), or field/remote-based (travel to visit customers, patients, or partners as needed). BMS supports accessibility and reasonable accommodations. If you require accommodations in the recruitment process, contact adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility for the Equal Employment Opportunity statement. BMS encourages vaccination and boosters for the well-being of employees and communities. BMS will consider qualified applicants with arrest and conviction records, where allowed by law. If you live or work in Los Angeles County, see California residents information for this role at careers.bms.com/california-residents/. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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Challenging. Meaningful. Life-changing. Bristol Myers Squibb offers work that transforms lives, with opportunities to grow and thrive alongside high-achieving teams. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of benefits, services and programs that support employees in pursuing their goals at work and in their personal lives. Read more about working with us on careers.bms.com. At
Bristol Myers Squibb
we are reimagining the future of cell therapy with a bold ambition and a best-in-class team, leading the way to unlock the full promise of cell therapy and put more patients on the path to a cure. If you are ready to challenge yourself and accelerate your career, there’s no better place than here at BMS with our Cell Therapy team. BMS Cell Therapy Manufacturing is seeking a
Senior Manufacturing Associate, Cell Therapy
to bring enthusiasm, intellectual curiosity, scientific rigor, and a drive to advance novel programs. The candidate should be goal-oriented, flexible, and able to work efficiently with safety and quality in mind. We are seeking enthusiastic and innovative individuals with a solid understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy. Shifts Available:
6pm - 6am, rotating shift including holidays and weekends, onsite. Responsibilities: Execute operations described in standard operating procedures and batch records. Demonstrate strong practical and theoretical knowledge in work. Complete documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. Solve simple problems; apply existing solutions from new perspectives. Perform tasks in a manner consistent with safety policies, quality systems, and GMP requirements. Complete training assignments to ensure necessary technical skills and knowledge. Train others on SOPs and Work Instructions to successfully complete manufacturing operations. Support investigations. Identify innovative solutions. Assist in setting up manufacturing areas and equipment/fixtures; perform facility and equipment commissioning activities. Write 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 complete manufacturing operations. Coordinate with production planning to execute daily unit operations schedules across multiple shifts. Work in a cleanroom environment and perform aseptic processing; maintain environmental conditions to meet health authority requirements. Knowledge and Skills: Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing. Ability to work assigned shifts (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. Preferred: aseptic processing in ISO 5 biosafety cabinets and universal precautions for handling human-derived materials in BSL-2 containment areas. Experience with cell expansion using incubators and single-use bioreactors. Basic Requirements: High school diploma and 3+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing, or relevant experience. Bachelor’s degree in a relevant science or engineering discipline with relevant experience strongly preferred. Working Conditions: Stand and walk for several hours at a time while operating manufacturing/computer equipment. Carry, lift, push, and/or pull up to 50 pounds several times a day. Climb steps or ladders several times a day. Bend and kneel several times a day. Overhead work and repetitive movements required several times a day. Wear PPE and clean room garments daily (safety shoes, safety glasses, gowns, hairnets, gloves, etc.). BMSCART #LI-ONSITE GPS_2025 If 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:
Devens - MA - US: $32.00 - $38.77 per hour. The starting compensation range for this role is listed above for a full-time employee basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account factors such as required skills, location, work schedule, and experience. Final compensation will be determined 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 careers.bms.com/life-at-bms. Benefit offerings are subject to the terms and conditions of the applicable plans and may include medical, dental, vision, wellbeing programs, 401(k), disability, life insurance, and other programs. Some programs provide paid holidays, vacation, volunteer days, sick time, and various leave options. Other perks include tuition reimbursement and a recognition program. Uniquely Interesting Work, Life-changing Careers With a vision like Transforming patients’ lives through science, each BMS employee contributes to work that goes beyond ordinary. We value passion, innovation, urgency, accountability, inclusion, and integrity. On-site Protocol BMS uses an occupancy structure to determine where an employee conducts their work. Roles may be site-essential (100% onsite), site-by-design (hybrid with at least 50% onsite), or field/remote-based (travel to visit customers, patients, or partners as needed). BMS supports accessibility and reasonable accommodations. If you require accommodations in the recruitment process, contact adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility for the Equal Employment Opportunity statement. BMS encourages vaccination and boosters for the well-being of employees and communities. BMS will consider qualified applicants with arrest and conviction records, where allowed by law. If you live or work in Los Angeles County, see California residents information for this role at careers.bms.com/california-residents/. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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