Manager, Business Process Delivery, Cell Therapy Manufacturing - Princeton, United States - Bristol-Myers Squibb Company

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**Manager, Business Process Delivery, Cell Therapy Manufacturing**

CAROUSEL_PARAGRAPH

Seattle, Washington; Leiden, Netherlands; Princeton, New Jersey; Summit, New Jersey

Manufacturing/Ops

R

Full Time

01/21/2022

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At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through science. In oncology, hematology, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

**Manager, Business Process Delivery** **, Manufacturing**

BMSs Cell Therapy business is entering an exciting new phase as it begins the commercialization of its first CAR-T products. Commercialization drives new scope, scale, and complexity across the network, and requires manufacturing sites, global organizations, and IT systems to work together in new ways.

The Manager, Business Process Deliver (Mgr. BPD) plays a key role in leading, analyzing, and delivering a portfolio of solutions that enhance and extend the capabilities offered to Manufacturing organizations and their close partners. The Mgr. BPD leverages knowledge of manufacturing processes and familiarity with manufacturing technology to either deliver solutions directly, or partner closely with IT Delivery teams to clarify detailed requirements and drive for technical solutions to be delivered right the first time with minimal need for rework.

The Mgr. BPD is a key member of cross-functional, cross-site communities within the Cell Therapy organization. The Mgr. BPD works collaboratively with Global and Local Business Process Owners, and the SC Portfolio & Project Management team to understand and influence the road map for desired scheduling capabilities.

**Responsibilities will include, but are not limited to, the following:**

Deliver user requirements for supply chain, quality, manufacturing, inventory warehousing and Order to cash. Lead solution designs that impact manufacturing , with a primary focus on supporting Cell Therapy requirements.

Act as a community expert for manufacturing process as its execution in planning systems. Actively engage with business partners and community members. Support and lead continuous improvement opportunities for SC processes

Support identifying and managing timelines, resources and tasks during all phases related with Supply Chain projects or initiatives, as well as ongoing business activities.

Work cross functionally, including with IT and other non- manufacturing process domains to support Cell Therapy

Facilitate use case for new system / software or enhancements related to ERP and ERP/MES. Drive workshops to ensure SCM functionality meets requirements

Responsible for executing validation testing including installation, operational and performance qualifications (IQ/OQ/PQ).

Deliver and maintain overall SAP SCM validation package

Develop, revise and review SOPs, qualification/validation protocols/package with ongoing awareness of changes in business and compliance requirements.

Collaborate with IT to oversee system implementation.

Assist in maintenance and creation of process documentation and work instructions

SAP Mfg owner for quality records including change controls, deviations and CAPAs. Point person to perform system change impact assessment

Coordinate successful rollout of ERP/MES changes including communications, training, support and documentation.

Partner with Mfg sites, Finance, and IT to implement and support a unified SAP system and release management process in compliance with GMP and SOX requirements

Develop and maintain training materials and provide system and process training

Document incidents and problems and corresponding solutions

SME on SAP Mfg/ SCM and supply chain processes

Serve as liaison for all system interface projects with SAP

Represent supply chain for all system interfaces projects with SAP.

Document/diagram E2E integrated process flows and business scenarios to ensure optimization and synchronization across all GMP systems and process

**Skills/Knowledge Required:**

Bachelors Degree in Supply Chain, Information Systems, Business or Engineering.

8+ years of experience in supply chain or manufacturing environment (pharmaceutical industry preferred).

8+ years of experience using SAP enterprise systems

Ability to work independently and cooperatively in a diverse group

Experience working in a manufacturing or supply chain organization or IT delivery team enabling manufacturing is a plus

Advance knowledge of personal computer applications such as Microsoft Office Suite

Demonstrated extensive experience with SAP Mfg, PP and SD.

Proven experience with SOX and GxP, and 21CFR part 11 requirements will be an advantage

Ability to travel 10%

Performed at least 1 (one) full life cycle implementation of SAP Modules

Managing medium- to large-scale projects

Management of a full-service end-user support

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture.

To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to . Visitto access our complete Equal Employment Opportunity statement.

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