DCM Quality Management - SAP

Bristol Myers Squibb•Princeton, NJ

8d•$175,346 - $214,940•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 SAP platforms and applications, third-party add-ons, and related tools in alignment with pharmaceutical industry needs. It manages SAP Quality Management (QM) Build & Run demand in the IT Portfolio, organizes resources, establishes priorities, and supports global manufacturing requirements through Software Development Life Cycle deliverables. Telecommuting is permitted up to two days per week. The position involves leveraging expertise in the SAP Stability Study sub-module, Quality Notifications, configuration, tables, data structures, BAPIs, and IDocs. It guides project teams and third-party development organizations in SAP QM and related applications, approves partner work, and manages transition of project work to partner teams. The role also supports audits and inspections and produces stakeholder presentations, memos, and documentation. The employer will accept a bachelor's degree or foreign equivalent in Mechanical Engineering or a related field, together with seven years of related work experience, including five years of progressive post-baccalaureate experience. The position requires experience with at least two full lifecycle implementations of SAP Quality Management and PP/PI for Discrete and Process Industries, as well as seven years of experience in the listed SAP, pharmaceutical, and lifecycle-management areas.

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 Quality Management 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 Quality Management 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 via the standard SAP QM-IDI interface.
Seven years of experience implementing and supporting SAP in the pharmaceutical industry and working with GXP processes regulated by the FDA.
Seven years of experience generating RICF documentation deliverables within Application Life-Cycle Management.

Responsibilities

Translate business requirements into solutions using SAP platforms 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.
Support groups by responding to audits and inspections.
Produce Software Development Life Cycle deliverables to support global manufacturing requirements.
Guide project teams and third-party development organizations in the SAP QM area and related applications.
Approve third-party and partner work in SAP or related applications.
Manage the transition of project work to partner teams.