Associate Director - Site Supply Chain Planning Global Process Leader (GPL) Location: New Brunswick - NJ - US, Cruiserath - IE, Manati - PR - US
Time Type: Full time
Posted On: 30+ Days Ago
Job Requisition ID: R1582365
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.
Position Summary
The Associate Director - Site Planning Global Process Leader (GPL) will be responsible for ensuring Internal and/or external site planning processes and digital capabilities are delivering with excellence for Biologics and Pharmaceutical commercial business units.
Key Responsibilities Forge a seamless relationship with all applicable cross functional stakeholders in the supply chain product space. In partnership with Business Unit SCPL Leadership Team, own the vision, roadmap, and prioritized book of work, for the pillar. Establish a highly structured, and standardized, ways of working across the impacted functional teams. Lead the delivery of digital first process enhancements to continuously improve core pillar capabilities. Prioritize and lead year over year initiatives to continuously enhance digital first SCPL capabilities. Establish seamless collaboration with other functional global process leaders, the center of excellence, IT and functional team members. Drive best practice adoption across Business Units. Ensure seamless alignment with priorities across Business Units. Own and continuously enhance the SCPL processes. Expansion into additional pillars of excellence is possible. Qualifications & Experience Undergraduate degree in supply chain, life science, business administration and/or engineering or equivalent required. Minimum 10+ years managing supply planning operations for a reputed global BioPharma or Consumer Product company. Experience in implementing world class, global supply chain planning processes and tools management. Experience in working in a fast paced, reputed, global pharmaceutical/Biotechnology or Consumer company. Strong Project Management capability skills. Demonstrated Operational Excellence and Continuous Improvement skill set and delivery. Preferred: Good understanding and exposure to current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) and other regulatory requirements. Thorough understanding of and experience with some aspect of technical operations. Personal Competencies Desired/Required Demonstrated experience in developing, aligning, socializing, monitoring, adapting, and delivering on complex deliverables. Interprets business challenges and recommends best practices-based solutions. Excellent verbal, written and interpersonal communication skills at all levels of the organization. Additional professional and personal requirements include: Executing for Results: Maintains high standards of performance for himself/herself and follows through on commitments. Leading / Supporting Cross Functional Teams: Ability to lead strong, diverse teams of people. Building Relationships: Establishes credibility and earns respect with a diverse set of cross functional stakeholders. On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role.
BMS is dedicated to ensuring that people with disabilities can perform complex functions through a transparent recruitment process, reasonable workplace adjustments, and ongoing support in their roles.
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