Specialist, CAR-T Supply Chain PPS

Bristol Myers Squibb Summit West - NJ - US Updated 24 August 2026
Pharma

Job description

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 . Specialist, CAR-T Production Planning and Scheduling Department: Breyanzi and Abecma Value Stream Location: Summit, NJ Position Summary The primary responsibility of this role is to schedule operations supporting clinical and commercial CAR-T manufacturing at the Summit West site. The role will require significant collaboration across internal and external functions to ensure on-time fulfillment of final product. The ideal candidate will have a demonstrated ability to balance multiple competing priorities, participate in projects, and follow Scheduling best practices. Duties & Responsibilities Create, maintain, and publish detailed finite schedules for operations including apheresis and PBMC/CMAT receipt, material kitting, cell processing, and media manufacturing. Serve as point of contact for the Manufacturing Operations organization and Value Stream functions including ECQ, Facilities, and Quality to provide support, facilitate operational continuity, and address issues as they arise. Complete all ERP lot creation and batch record request tasks required for weekly document issuance. Collaborate with cross-functional business partners such as OpEx, IT, Materials Management, Master Data Management, and Manufacturing Technical Services on system implementations, continuous improvement projects, and software/dashboard development. Perform other tasks as assigned. Reporting To: Associate Director, Value Stream Planning Qualifications Knowledge, Skills & Abilities: Understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique Knowledge of cGMP/Pharmaceutical regulations Proficient in planning/ERP systems (SAP) and analytics tools Advanced proficiency in MS Office applications Strong written and verbal communication skills Proficient presentation development and delivery skills Ability to identify continuous improvement opportunities Ability to work independently and as part of a team Ability to solve routine and complex problems Ability to provide on-call support for emergent issues Education & Experience: Bachelor's degree required 2–3+ years of relevant work experience, preferably in a regulated pharmaceutical manufacturing environment 1+ years of experience as a production scheduler or planner 1+ years of experience supporting ERP systems (preferably Oracle or SAP) An equivalent combination of education, experience, and training may substitute Working Conditions Intermittent walking and sitting; ability to sit or stand for extended periods may be necessary Physical dexterity sufficient to use computers and documentation Sufficient vision and hearing capability to work in the job environment Ability to lift up to 25 pounds Must be able to work around laboratories and controlled, enclosed, restricted areas Cleanroom garments and PPE required in designated areas Makeup, gum, nail polish, or other potential microbial sources are prohibited in restricted areas Clean room environment includes assigned pressure and temperature conditions; exposure to reagents, chemicals, and sanitization agents is expected Routine exposure to human blood components Designated areas may prohibit food and outside materials (e.g., cell phones, tablets) Travel: Less than 10% 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: Summit West - NJ - US: $33.49 - $40.59per hour
 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. 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 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 benefits include: Health Coverage: Medical, pharmacy, dental, and vision care. Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. ​ Work-life benefits include: Paid Time Off US

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