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Senior Manager, Cell Therapy Receiving and Warehousing in Devens, MA

Bristol Myers Squibb
Devens - MA, United States, United Statesfull_timeVerifiedPosted 26 Nov 2025
💰 $148,413/yr($122,480/yr$148,413/yr)

About the role

Working with Us
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.

The Senior Manager, Cell Therapy Receiving and Warehousing is accountable for the overall performance and operations of the warehouse and receiving dock at the Cell Therapy Facility. The Senior Manager provides oversight for raw material and consumable receipt, put-away, replenishment, management, and destruction for Manufacturing, Quality Control, and Facilities materials used directly and indirectly to support the manufacture and testing of commercial and clinical Cell Therapy products.

This is a direct people manager role overseeing a team of material handlers within the nonclassified CGMP receiving dock, Warehouse, and controlled storage locations.

Shifts Available:

TBD

Responsibilities:

People Leadership:

  • Develop and manage team member resource allocation & shift schedules to meet workflow demands as a manager of individual contributors.
  • Coach and counsel team members to develop their skill sets and create an environment of continuous learning, teamwork, transparency and a sense of urgency.
  • Communicate with cross-functional leaders inside and outside of Supply Chain to drive successful outcomes for the site and functional business unit.
  • Maintain and communicate performance metrics for team, setting and maintaining high expectations for team performance.

Material Receiving & Warehousing:

  • Manage raw material/consumable receipt, labeling & storage.
  • Conduct investigations and root cause analyses on any supply disruptions or material quality issues, report on corrective actions.
  • Oversee shipment of materials to offsite locations (network warehouses, offsite storage locations, centralized QC testing labs, etc.,).
  • Develop & maintain metrics.
  • Serve as process owner and subject matter expert to help remove barriers and solve problems within department

Manage Area Quality Systems & Compliance:

  • Ensure a safe work environment is maintained in all areas where group activities occur.
  • Promote and engage team in safety and safety training program; foster a culture of compliance and strong environmental, health, and safety performance.
  • Manage Site Supply Chain Standard Operating procedures.
  • Own and manage deviations, corrective/preventive actions & change controls.
  • Ensure appropriate training and qualification for staff activities performed.
  • Foster a culture of compliance and strong environmental, health, and safety performance.

Operational Excellence:

  • Promote a mindset of continuous improvement, problem solving, and prevention.
  • Participate in and/or lead cross-functional

Knowledge, Skills, Abilities:

  • Preferred but not required: Certification in CPIM, CSCP, and/or CLTD
  • Experience within Commercial / Clinical Biotechnology environment is preferred
  • Experience with people management is required
  • Experience with Health Authority Audits (i.e. FDA) is required

Minimum Requirements:

  • Bachelor’s degree required in Life Sciences, Supply Chain, or similar.
  • 7+ years relevant work experience required.
  • 3+ years of expe

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Company

Bristol Myers Squibb

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