Huguenot, New York Bristol-Myers Squibb

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: .

Responsibilities:

• Drive meetings sets that are elements of the F&OP business process and monthly cycle. Continue to formalize this nascent process by championing improved structure, stakeholder engagement and process maturation.
• Maintain and continuously improve the F&OP business process in concert with the process owner(s). Participate day-to-day in administering the process, ensure process documentation remains accurate, and develop the process to meet evolving requirements.
• Actively work in IBP (Integrated Business Planning) digital planning system, ensuring monthly operators, and other regular calendar driven activities are occurring per design.
• Interact with IBP to perform manual adjustments (e.g. inventory loading) are executed, and Master Data is maintained. Facilitate complete and robust data sets within IBP, and instill confidence in stakeholder perspective on IBP as single source of truth for R&D supply chain planning.
• Maintain accountability for R&D Supply Chain dashboards, analytics and reports. Further build capabilities per F&OP stakeholder Voice of Customer and evolving requirements. Act as point of contact with IT design team fulfilling dashboarding requirements.
• Act as interim Business Process Manager (BPM) for seven Level-1 processes which are part of the R&D Supply Chain planning model. Apply a disciplined approach to execute, document, measure, monitor, and control both automated and non-automated business processes. Facilitate improved process metrics, KPIs and reporting which drive process both management and continuous improvement.

Requirements:

• Operate with a high degree of connectedness, transparency and clarity to ensure common understanding of requirements, issues and actions; listen to stakeholders and distill information into pertinent and actionable content.
• Demonstrate a nimble nature to adapt to the pace and dynamic nature of an R&D environment; process data, information and feedback with speed and communicate outcomes, alternatives and actions plans with appropriate urgency.
• Proactively approach change management and model ideal behaviors and actions; foster growth of employees through inspiration, innovation and advocating of the value and case for change.
• Use critical thinking to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems. Must possess initiative with strong analytical and problem solving skills.
• Face multiple upstream and downstream stakeholders, and through regular interactions, develop trusted relationships to enable efficient operations; leverage a wide sphere of influence; pressure test demand requirements and supply constraints constructively and negotiate bi-directionally to develop balanced outcomes.
• Prior experience within a supply chain function; familiarity and operation within an S&OP process; knowledge of regulatory and GMP frameworks related to clinical use of bulk drug substance and drug product; knowledge of the drug development process and clinical trials; APICS certifications; 5-7 years biopharmaceuticals industry planning experience.

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

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 . Visit eeo -accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

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

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.