DCM Quality Management - SAP

Bristol Myers Squibb•Princeton, NJ

8d•Hybrid

About The Position

Bristol Myers Squibb is hiring a DCM Quality Management - SAP professional in Princeton, New Jersey. The role translates business requirements into solutions using the SAP platform and applications, third-party add-ons, and related tools, aligned with the pharmaceutical industry. It manages SAP Quality Management (QM) Build & Run demand in the IT Portfolio and guides project teams and third-party development organizations across SAP QM and related applications. The position supports global manufacturing requirements by producing Software Development Life Cycle deliverables, maintaining system design and testing procedures and quality standards, and responding to audits and inspections. Telecommuting is permitted up to two days per week. The employer will accept a bachelor's degree or foreign equivalent in Mechanical Engineering or a related field, along with seven years of related work experience, including five years of progressive post-baccalaureate experience. The role requires experience with full lifecycle SAP QM and PP/PI implementations, SAP module integration, pharmaceutical and FDA-regulated GXP processes, LIMS interfaces, and Application Life-Cycle Management documentation.

Requirements

Bachelor’s degree or foreign equivalent in Mechanical Engineering or a related field.
Seven years of related work experience, including five years of progressive post-baccalaureate experience.
Experience with at least two full lifecycle implementations of SAP Quality Management and Production Planning (Manufacturing) for Discrete and Process Industries (PP/PI).
Seven years of experience integrating SAP QM with PP/PI (Discrete and Process Manufacturing), MM (Material Management), IM (Inventory Management), and WM/EWM (Warehouse and Extended Warehouse Management).
Seven years of experience maintaining SAP QM master data, including Master Inspection Characteristics, Inspection Plans, Inspection Methods, Quality Profiles, Catalogs, Code Groups, Sampling Procedures, Sampling Schemes, Dynamic Modification Rule, and Material Master.
Seven years of experience integrating SAP requirements with external LIMS through the standard SAP QM-IDI interface.
Seven years of experience implementing and supporting SAP in the pharmaceutical industry and working with FDA-regulated GXP processes.
Seven years of experience generating RICF documentation deliverables within Application Life-Cycle Management.

Responsibilities

Translate business requirements into solutions using SAP platform and applications, third-party add-ons, and related tools.
Collaborate with internal teams and external partners to manage project timelines, budgets, and deliverable quality.
Define system goals and create flow charts and diagrams describing logical operational steps of programs.
Create presentations, memos, and documentation for multiple stakeholders.
Organize resources, establish priorities, and manage SAP QM Build & Run demand in the IT Portfolio.
Develop, document, and revise system design procedures, test procedures, and quality standards.
Use expertise in SAP Stability Study sub-module, Quality Notifications, configuration, tables, data structures, BAPIs, and IDocs.
Support groups responding to audits and inspections.
Produce Software Development Life Cycle deliverables supporting global manufacturing requirements.
Guide project teams and third-party development organizations in SAP QM and related applications.
Approve third-party and partner work in SAP or related applications.
Manage the transition of project work to partner teams.