Senior Manager, Site Supplier Liaison Lead

2 days ago

New Brunswick, New Jersey, United States Bristol-Myers Squibb Full time
Transforming Patients' Lives through Science

Bristol-Myers Squibb is a leading pharmaceutical company dedicated to transforming patients' lives through science. We are seeking a highly skilled and experienced Senior Manager, Site Supplier Liaison Lead to join our team.

About the Role

The Senior Manager, Site Supplier Liaison Lead will be responsible for developing and implementing stakeholder forums to enable strong connectivity between the BMS site supplier functions and the central supplier management functions. This role will drive alignment and harmonization in the implementation and ongoing maintenance of all aspects of the supplier management lifecycle across BMS Network sites in Biologics/Pharma/Cell Therapy Ops.

Key Responsibilities
  • Develop and implement stakeholder forums to enable strong connectivity between the BMS site supplier functions and the central supplier management functions.
  • Drive alignment and harmonization in the implementation and ongoing maintenance of all aspects of the supplier management lifecycle across BMS Network sites in Biologics/Pharma/Cell Therapy Ops.
  • Support and represent SQE at site quality councils and material review boards, as required.
  • Support the Supplier Change process for site material inventory management.
  • Collaborate with the acquired company's supplier/vendor management team(s) to ensure a smooth transition and alignment of goals and objectives.
  • Facilitate effective communication and change management strategies to keep SQE team informed and engaged throughout the integration process.
  • Monitor and track progress against SQE assigned integration milestones, identifying and addressing any issues or roadblocks that may arise.
  • Continuously evaluate and refine integration strategies and plans based on feedback, lessons learned, and changing business needs.
  • Develop and manage the resource and capacity model and execute workload management for the supplier quality excellence team.
Requirements
  • Bachelor's degree in science, or a related field.
  • 8+ years of experience in a pharmaceutical/biopharmaceutical/Advanced Therapeutic Modality Products (ATMP) environment including previous QA experience - e.g., QA compliance role, Supplier Quality oversight and 2+ yrs managing matrix teams and 4+ years project mgmt. experience. ATMP experience a plus.
  • Deep understanding of supplier management principles, governance frameworks, and performance metrics.
  • Advanced operational excellence skills preferred such as process excellence/six sigma methods and approaches including process mapping, root cause analysis and problem definition.
  • Strong change leadership skills.
  • Demonstrated ability to work in a matrixed organization with diverse teams and to influence areas not under direct control.
  • Strong leadership and stakeholder management skills, with the ability to influence and collaborate effectively with cross-functional teams.
  • Demonstrated ability to wield and develop technologies, innovations, programs, and procedures that move the business forward.
  • Excellent communication and presentation skills, with the ability to convey complex information to diverse audiences.
  • Demonstrated innovation, flexibility, open-mindedness, and adaptability to meet objectives in a rapidly changing environment with shifting priorities.
  • Strong decision-making capability and ability to think conceptually and understand impact of decisions.
  • Ability to work independently and prioritize tasks effectively in a fast-paced environment.
  • Mastery in using quality management and analytical software and tools. Veeva Quality Suite and Tableau experience a plus.
What We Offer

Bristol-Myers Squibb offers a competitive benefits package, including a comprehensive health insurance program, 401(k) plan, and employee stock purchase plan. We also offer a range of employee development programs, including training and education opportunities, mentorship, and career advancement opportunities.

We are an equal opportunity employer and welcome applications from diverse candidates. If you are passionate about transforming patients' lives through science and have the skills and experience required for this role, please submit your application.

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