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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.

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 Associate Director, Site Supply Chain Systems , is responsible for leading a team of people who manage, implement, and execute support of site ERP systems and supply chain related systems to maintain a compliant, effective, and efficient operation that meets or exceeds site goals and objectives. This role will take ownership to develop and deliver solutions that address process gaps that benefit the patients we serve.

Shifts Available:

Monday - Friday, Standard Working Hours

Responsibilities:

• Lead and develop members of the Site Supply Chain Systems group

• Assist in designing, testing, and maintaining manufacturing data, including, but not limited to, items, specifications, lookups, list of values, recipes, routings, formulas, process instructions, and process variables

• Develop and execute cGMP change controls and ServiceNow change requests for master data changes

• Collaborate within the department and with manufacturing, quality control, quality assurance, IT, global master data management, and supply chain organization to determine business requirements for the design of master data

• Translate business requirements into a robust data design which is compliant, efficient, and effective

• Coordinate the testing of master data with peers and internal customers to ensure business requirements are achieved

• Run the recipe release process to meet manufacturing requirements and to maintain compliant, efficient, and reliable batch records and supporting data

• Collaborate with other stakeholders (global and site) to maintain and optimize product hierarchy while maintaining compliance and minimizing risk; scope includes cell therapy sites (Summit, Warren) and collaboration with above site departments and other cell therapy locations

• Provide direct, internal, supply chain related customer support to manufacturing, site planning, inventory control, quality assurance, quality control, global master data management, and IT

• Develop and provide technical training to ERP users

• Maintain an understanding of the manufacturing processes and associated ERP system (Oracle, SAP, etc.)

• Provide support to internal customers for system issues

• Perform other tasks as assigned in area of responsibility

Basic Requirements:

• BS or BA degree in computer science,"supply chain management,"or related field required

• At least 7 years experience working in a Pharma/Med Device environment, or similar regulated industry

• At least 5 years experience with enterprise data applications with 3-5 years in a data management role desired, preferably in biotechnology or pharmaceutical manufacturing or other GXP environments

• Knowledgeable on current"data management techniques"

• ERP System experience in Oracle and SAP, including implementations, preferred

• APICS/CPIM or equivalent certification desired

• Skilled in project management

• People leader experience preferred

• Lean/continuous improvement certification a plus

• Interpersonal and facilitation skills are necessary to interface with and influence various levels of the organization

• Proven ability to adjust to multiple demands, shifting priorities and unexpected events while maintaining a positive work attitude

BMSCART

#LI-ONSITE

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.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://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.

Company: Bristol-Myers Squibb

Req Number: R1588891

Updated: 2025-01-27 03:50:41.605 UTC

Location: Summit West-NJ

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.