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.

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

Position Summary

The DCM Quality Management – SAP is responsible for driving solutions to enable effective and efficient outcomes for the BMS business. Through strong collaboration and a focus on business success, this person drives BUILD and RUN activities for the Quality Management functionalities associated to the SAP systems.

Key Responsibilities

• Working knowledge and experience with SAP Quality Management (QM), Production Planning (Manufacturing) for Discrete & Process Industries (PP/PI)
• Working knowledge and experience with the integration requirements of SAP S4/HANA QM (Quality Management) with PP/PI (Discrete and Process Manufacturing), MM (Material Management), IM (Inventory Management), and WM/EWM (Warehouse and Extended Warehouse Management-Embedded) functionality.
• Working knowledge and experience with the maintenance requirements of all Quality related master data, such as Master Inspection Characteristics, Inspection Plans, Inspection Methods, Quality Profiles, Catalogs/Code Groups/Codes, Sampling Procedures/Sampling Schemes, Dynamic Modification Rule and the manufacturing and integration data required in the Material Master.
• Working knowledge and experience with the integration requirements of SAP with different external LIMS (Laboratory Information Execution Systems) via the standard SAP QM-IDI interface.
• Working knowledge of integration middleware (WebMethods) and how it is used with Interfaces between SAP and LIMS / other Quality and Manufacturing systems.
• Working knowledge in the SAP Stability Study sub-module and Quality Notifications.
• Able to debug ABAP programs or follow the programming logic at a higher level and be able to write pseudo code and write detailed functional and technical specifications.
• Understand the technical structures in the SAP system such at tables, table relationships, data structures, function modules BAPI, BADI, RFC, Logical Destinations, IDocs, etc.
• Know the configuration, tables, data structures, BAPI’s and IDocs to support your functional area of expertise.
• Ability to produce clear and effective written presentations, memos, etc.
• Able to effectively translate business requirements to a solution using the SAP platform and applications and 3rd party bolt/add-ons and related platform tools.
• Understands pharmaceutical industry dynamics – proactively and reactively applies this knowledge when making decisions
• Develops self through training and project work assignments
• Identifies and leverages synergies with other projects and/or processes

Qualifications and Experience

• Able to organize resources, establishing priorities and manage the SAP QM Build & Run demand in the IT Portfolio.
• Able to work with our delivery partner (Accenture) in developing cost estimates in a timely fashion
• Routinely work with including leading teams composed of EG-130 / EG-140 / EG-150
• Able to influence Associate Director and Director level with oral and written presentations
• Ability to produce clear and effective written presentations, memos, etc.
• Able to respond to and support multiple groups for Audits and inspections.
• Part of the team that produces the deliverables as specified by Software Development Life Cycle (SDLC) to support the Manufacturing requirements globally.
• Deliver on all project timelines, project budget, and overall project quality.
• Providing solutions by using the SAP applications as well as related bolt-on, related tools, and integrations tools
• Provide oversight and guidance to project teams and third party /partner development organizations for the Quality Management (QM) area and related applications.
• Provide approval as necessary for third party and/or partner work in the SAP or related applications
• Managing/Guiding the transition of all project work to the Accenture build and run teams
• Provide oversight and governance for process design within the SAP S4/HANA platform in the specific area of SAP QM
• Model the BMS core behaviors – Accountability, Speed, Passion and Innovation

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

COVID-19 Information
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.

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/eeo-accessibility to access our complete Equal Employment Opportunity statement.

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

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