DCM Quality Management - SAP

Bristol-Myers Squibb Co; Princeton (NJ); Hybrid; USD 175,000 - 215,000; Full time

Benefits offered by this job

Healthcare benefits

Leave benefits

Retirement benefits

Job summary

Bristol-Myers Squibb Company is recruiting for a DCM Quality Management - SAP role in Princeton, NJ. The position focuses on translating business requirements into SAP solutions, managing QM Build & Run, and ensuring quality across the SAP landscape.

The role requires deep SAP QM experience, integration with PP/PI, MM, IM, and WM/EWM, and strong collaboration with internal teams and external partners. Telecommuting up to two days per week is allowed.

Qualifications

• Bachelor’s degree or foreign equivalent in Mechanical Engineering or related field, and seven years of related work experience.

Responsibilities

• Translate business requirements into SAP solutions and related tools.
• Define system goals and develop flow charts and diagrams for programs.
• Organize resources and manage SAP QM Build & Run in IT Portfolio.
• Develop, document and revise system design procedures and quality standards.
• Support audits and inspections and respond to regulatory requirements.

Skills

SAP QM expertise

Tools

SAP

Job description

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. 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 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: $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. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

For roles based in Washington State only: If you live in or expect to work from Washington State if hired for this position, please visit this page for important information about the Washington Fair Chance Act.

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If this posting is missing required information required by local law or incorrect, contact BMS at [e-mail] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1603195 : DCM Quality Management - SAP Data Privacy Link

We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.