Associate Director, CAR-T Site Supply Chain Product Planner

3 weeks ago

Summit, United States Bristol Myers Squibb Full time

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 rich in diversity. Take your career farther than you thought possible.

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 Associate Director CAR-T Site Supply Chain Product Planner is a planning role in the Cell Therapy Operations Summit West (CTO SMW) New Jersey manufacturing site. The product planner will be responsible for the short-term product schedule and end to end planning of that product. The product planner will be responsible for coordinating, planning, scheduling, and ensuring routine, timely delivery of product. This role will report directly to Supply planning Director and sit on the Product Specific Value Stream team representing Supply Chain.

Responsibilities:

Develop and maintain a product supply plan for the short-term horizon, incorporating equipment, media, raw materials, vector and LN2 planning.

Develops and owns raw material transition plans.

Analyze data and metrics to optimize the schedule and improve overall efficiency.

Owns inventory and inventory reporting for the respective product.

Supports product launches by ensuring master data is setup and supply chain readiness.

Coordinate with a cross-functional team to gather inputs and updates to maintain the supply plan.

Work closely with the detailed scheduling team to hand-off the finite schedule and continuously work to improve scheduling process and tools to enhance productivity and accuracy.

Ability to implement new technology into the planning process to automate and streamline communication.

Represent supply chain on the Product Value Stream team.

Knowledge & Skills:

Deep understanding and/or experience in supply chain planning and scheduling.

Continuous improvement mindset with ability to identify and implement changes.

Experience utilizing and implementing systems to increase planning connectedness and productivity.

Flexible and comfortable working with ambiguity.

Strong interpersonal and teamwork skills; ability to develop and maintain effective professional relations with colleagues at all levels across the organization.

Strong understanding of current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) and other regulatory requirements (EMA, TGA).

Basic Requirements:

Bachelor’s degree in supply chain, engineering, life sciences, business management or related fields.

8-10 years of experience in the biopharmaceutical and/or biotechnology industry.

7-10 years of experience in production planning.

7-10 years of experience in GMP supply chain.

3 years of experience with raw materials (with understanding cut over strategies).

ERP systems experience (Oracle and/or SAP with SAP preferred).

Production scheduling experience.

Preferred Requirements:

Green Belt Certified.

Operational Excellence experience.

Strong influencer.

#BMSCART,

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