DCM Quality Management - SAP

Bristol-Myers Squibb; United States; Hybride; USD 175 000 - 215 000; Plein temps

Résumé du poste

Bristol Myers Squibb in Princeton, NJ is seeking a DCM Quality Management - SAP expert to translate business requirements into SAP QM solutions and manage the SAP QM Build & Run demand within the IT portfolio.

You will guide project teams, collaborate with internal and external partners, and support audits and inspections while ensuring quality across global manufacturing activities. Telecommuting up to 2 days per week may be available.

Qualifications

• Bachelor's degree or foreign equivalent in Mechanical Engineering or related field.
• 7+ years of related work experience, of which five (5) years must be progressive post-baccalaureate experience.
• Experience in SAP QM implementations (2+ full lifecycle projects)

Responsabilités

• Translate requirements into SAP QM solutions and applications.
• Lead SAP QM projects with internal teams and external partners to manage timelines, budgets, and quality.
• Define system goals and create flow charts describing logical steps of programs.
• Develop, revise, and document system design procedures, test procedures, and quality standards.
• Support audits and inspections and respond to regulatory requirements.
• Mentor project teams and approve third-party work in SAP QM and related applications.

Connaissances

SAP QM

Quality Management

Project management

GxP compliance

Formation

Bachelor's degree in Mechanical Engineering or related field

Outils

BAPI/IDocs

LIMS integrations

Description du poste

DCM Quality Management - SAP (in Princeton, NJ)

At Bristol Myers Squibb, our employees often ask, "Who are you working for?"-a 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.

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.
• 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

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.

How We Work

Where you work matters - because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

Supporting People with Disabilities

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. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.