Drive end-to-end supply solutions within Cell Therapy program teams and Global Supply Chain
Develop multi-year supply strategy
Advise and influence the implementation strategies for supply-related changes, in collaboration with cross-functional and functional team members
Develop and implement strategies for managing supply fragmentation
Guide the inventory strategy for critical "make" items (i.e. vector, plasmids, RNPs, etc.)
Identify and escalate supply risks and propose solutions
As required, provide and present supply chain updates to Cell Therapy Governance bodies
Ensure alignment of Global Supply Chain, Manufacturing, and Clinical Operations understanding of current program objectives, facilitate escalations, and drive solutions
Promote a mindset of continuous improvement, problem-solving, and prevention
Build and maintain positive relationships with functions across the Cell Therapy network
Performs other tasks as assigned
Up to 15% travel, domestic and international
Qualifications & Experience:
BA/BS degree in supply chain, engineering, life sciences, or related fields
8+ years of related experience in supply chain, GMP manufacturing, or clinical operations in a biopharma environment
3+ years of experience leading teams
Experience in Cell Therapy, supply chain systems, and product lifecycle management highly desired
Demonstrated knowledge of operational supply chain execution and matrix team management
Effective oral and written communication
Demonstrated business acumen, with ability to deliver executive level presentations, challenge assumptions, and drive decision-making
Able to evolve with the needs of a dynamic and/or ambiguous environment
Experience with current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) and other regulatory requirements (EMA, TGA)
#LI-Hybrid
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: $179,590 - $217,618
Madison - Giralda - NJ - US: $167,840 - $203,384
Princeton - NJ - US: $167,840 - $203,384
Seattle - WA: $184,620 - $223,716
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our bene
Benefits
Equity / stock options
Additional Information
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 .
The Associate Director, Supply Chain Product Lead (SCPL) represents Global Supply Chain for clinical phase products in the BMS Cell Therapy pipeline. The SCPL is a core member of critical matrix teams for assigned programs (i.e. CMC Team, GO Team, and associated sub-teams) and leads a matrixed supply chain sub-team. This individual may also be a people manager/leader for a small direct team.
The SCPL collaborates with key stakeholders to develop and evolve multi-year supply strategies, translates supply-related program deliverables and risks into the Supply Demand & Operations Planning (SD&OP) process, and drives end-to-end supply solutions in collaboration with functional and cross-functional team members. The SCPL routinely interacts with members of Development CMC, Product Operations, Manufacturing Sciences & Technology, Product Quality, Regulatory CMC, internal and external manufacturing, Patient Operations, Global Supply Chain functions, and Clinical Development to develop and drive a holistic strategy for the program supply.