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Associate Director, Supplier Relationship Management

Bristol Myers Squibb
New Brunswick, United Statesfull_timeVerifiedPosted 13 Jun 2024

About the role

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: careers.bms.com/working-with-us.

Required Qualifications:

  • Bachelors or Master's Degree in Engineering, Biotechnology, or related field.

  • 10+ years of relevant experience in the pharmaceutical, biopharmaceutical or related industry     

  • Certification in lean manufacturing principles and Six Sigma tools

  • Operations experience in pharmaceutical manufacturing to cGMP standards including extensive knowledge of regulatory guidelines and validation practices

  • Working knowledge of pharmaceutical development and commercialization processes.

  • Knowledge of suppliers, industry trends and emerging players in global pharmaceutical manufacturing services

  • Strong presentation and communication skills both, oral and written - Fluency in English

Additional Qualifications:

  • Strong ability in negotiating and influencing without authority in complex, high impact situations

  • Successful track record in execution and completion of objectives.

  • Ability to apply technical and cross-functional expertise to address complex operations problems.

  • Ability to effectively transfer complex knowledge regarding science and engineering procedures.

  • Demonstrated team leadership skills and ability to work effectively with cross-functional & multi-location teams

  • Demonstrated financial and project management skills

  • Demonstrated capability in implementing challenging goals, objectives and practices in a complex and ambiguous environment

  • Demonstrated success negotiating complex supply and toll manufacturing agreements with external suppliers.

  • Experience of a culturally diverse workplace through international projects or global teams.

  • Strong strategic and analytical thinking, problem solving and rapid decision making skills

  • Demonstrated proficiency in competency areas of Strategic Agility, Organizational Agility, Business Acumen, Process Design and Management, Organization Change Management

Key Responsibilities:

  • Establish and lead the Virtual Plant Team model

  • Act as a primary point of contact for all business collaborations ensuring that the overall relationship is healthy:

  • Responsible for performance monitoring & reporting and ensuring compliance with contractual terms

  • Collaborate with Quality Operations on quality system and compliance activities

  • Drive continuous improvement of the overall business relationship

  • Collaborate on forecasting, production planning and supply chain business process activities to ensure continuity of supply and avoidance of back-orders Act as primary point of contact for communications and resolution of supply chain and technical issues that may impact timely supply of product and/or contractual obligations

  • Proactively identify supply risks and create strategies to avoid or minimize their impact

  • Manage inventory risk assessment process for inventory located at manufacturing site. Lead efforts to manage and execute risk mitigation plans.

  • Lead cross functional teams in implementing and managing processes between BMS, internal sites and CMOs.

  • Accountable for establishing and managing the technical transfer start-up and spend budgets for assigned manufacturing site and the associated variances.

  • Identify opportunities for improvements and execute Operational

  • Excellence and Process Improvement/Best Practices.

  • Establish Standard Business Processes to accelerate pipeline development, commercialization  and end to end supply chain excellence

  • Identify, evaluate, select

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Company

Bristol Myers Squibb

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