DCM Quality Management - SAP

Duties: Translate business requirements into solutions using SAP platform and applications, third-party add-ons, and related tools in alignment with the pharmaceutical industry’s dynamics. Identify and leverage synergies in collaboration with internal teams and external partners to manage project timelines, budget, and quality of deliverables. Define the goals of the system and devise flow charts and diagrams describing logical operational steps of programs. Create presentations, memos, and documentation for multiple stakeholders. Organize resources, establish priorities, and manage the SAP Quality Management (QM) Build & Run demand in the IT Portfolio. Develop, document, and revise system design procedures, test procedures, and quality standards. Leverage expertise in SAP Stability Study sub-module, Quality Notifications, configuration, tables, data structures, BAPI’s, and IDocs. Support various groups by responding to audits and inspections. Produce deliverables as specified by Software Development Life Cycle to support the global manufacturing requirements. Guide project teams and third-party development organizations in SAP QM area and related applications. Provide approval for third-party and partner work in SAP or related applications. Manage the transition of project work to the partner teams. Telecommuting permitted up to 2 days per week.

REQUIREMENTS: Employer will accept a Bachelor’s degree or foreign equivalent in Mechanical Engineering, or a related field, and seven (7) years of related work experience, of which five (5) years must be progressive post-baccalaureate experience. Related skills required.

Bristol-Myers Squibb Company is hiring a(n) DCM Quality Management - SAP (in Princeton, NJ).