DCM Quality Management SAP

At Bristol Myers Squibb our employees often ask Who are you working fora question that fuels collaboration accountability and urgency in our work. Our purpose-driven culture inspires us to discover develop and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work opportunities for growth and a supportive environment that values inclusion wellbeing flexibility and comprehensive benefits. This is work that transforms the lives of patients and the careers of those who do it.

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

Duties: Translate business requirements into solutions using SAP platform and applications third-party add-ons and related tools in alignment with the pharmaceutical industrys 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 BAPIs 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 Bachelors 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.

Must have experience in at least 2 full lifecycle implementations of SAP Quality Management Production Planning (Manufacturing) for Discrete & Process Industries (PP/PI).

Must have seven (7) years of experience with/in:

• Integrating the SAP Quality Management module with other modules including PP/PI (Discrete and Process Manufacturing) MM (Material Management) IM (Inventory Management)
  and WM/EWM (Warehouse and Extended Warehouse Management);
• 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;
• Integrating requirements of SAP with different external LIMS (Laboratory Information Execution Systems) via the standard SAP QM-IDI interface;
• Implementing and supporting SAP in the pharmaceutical industry and working with GXP relevant processes that are regulated by the FDA; and
• Generating RICF documentation deliverables within the Application Life-Cycle Management.

Salary: $175346 to $214940 per year Additionally employees are eligible for an annual discretionary bonus and benefits including healthcare leave benefits and retirement benefits. BMS operates a pay-for-performance compensation philosophy and your total compensation may vary based on role location and firm department and individual performance. Contact: Bristol-Myers Squibb Company at and use ref. Number R1603195

We hire for skills and capabilities not just credentials if this role excites you but doesnt perfectly match your resume we encourage you to apply anyway.

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