Associate Director Long-range Supply and Capacity - New Brunswick, United States - Bristol-Myers Squibb
Description
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:
Associate Director Long-Range Supply and Capacity Planning - GPL
Location:
New Brunswick, NJ
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, Long Range Supply and Capacity Planning Global Process Leader is responsible for E2E cross functional excellence in the Long-Range Supply and Capacity Planning pillar within the Biologics, Pharmaceuticals and Cell Therapy Commercial Business Units.
Key Responsibilities
Forge a seamless relationship with all cross functional stakeholders in the Strategic Network Planning space to ensure enterprise needs from the long range supply and capacity planning pillar are understood, problems are addressed, and the pillar is represented with a consistent message.
In partnership with Business Unit Long Range Planning 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 Long-Range Supply and Capacity Planning teams that will deliver continuous value add initiatives.
Own core Long Range Supply and Capacity Planning KPIs that will measure the effectiveness of overall planning capabilities to drive data driven decision making.
Lead the delivery of digital first process enhancements to continuously improve core pillar capabilities that will drive enterprise performance and decision making in the strategic network planning space.
Establish improve seamless collaboration with other functional global process leaders, the center of excellence, IT and functional team members to ensure functional hand offs are complementary, with limited overlap, to drive excellence in our ways of working.
Ensure seamless alignment with priorities across Business Units
Own and continuously enhance the Long-Range Supply and Capacity Planning process.
Expansion into additional pillars of excellence is expected.
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 utilizing world class planning and execution processes and supported by ERP and Advanced Planning Systems (experience with SAP suites and Kinaxis Rapid Response software)
- Experience in implementing world class, global supply chain planning processes and tools management through deployment of global advanced planning and scheduling systems as well as performance management.
- Experience in working in a fast paced, reputed, global pharmaceutical/Biotechnology or Consumer company organized in a matrix structure.
- 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; interest and demonstrated ability to learn across several disciplines (manufacturing, quality, supply chain, technical development, regulatory, patient experience, finance, operations, etc.)
Personal Competencies Desired/Required:
- Demonstrated experience in developing, aligning, socializing, monitoring, adapting, and delivering on complex deliverables in dynamic, rapidly changing
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