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Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Director, ASAT Systems and Technology Sciences

Biology & BiotechConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A bachelor's degree in a scientific, engineering, information systems, or related discipline is required; an advanced degree (MS or PhD) is preferred.
  • At least 12 years of relevant experience, or an equivalent combination of education and experience, within biotechnology, pharmaceuticals, cell therapy, gene therapy, or biologics manufacturing environments.
  • At least 6 years of leadership experience managing technical teams and complex cross-functional programs.
  • Demonstrated experience leading network-scale laboratory systems, digital transformation, automation, informatics, quality systems, or technology-enabled business initiatives.
  • Proven success developing and executing strategic roadmaps that drive operational excellence, compliance, scalability, and business value.
  • Demonstrated ability to influence senior leadership and lead large, complex, high-risk, or high-visibility programs across multiple sites, functions, and technology platforms.
  • Extensive knowledge of GMP regulations, data integrity principles, quality systems, risk management, and commercial manufacturing operations.
  • Strong enterprise mindset and business acumen, with the ability to balance operational needs, regulatory requirements, and long-term business objectives.
  • Demonstrated leadership, influencing, and stakeholder-management skills, including driving alignment across Quality, Manufacturing, Technical Operations, IT, and other cross-functional organizations.
  • Demonstrated ability to identify emerging technologies, industry trends, and innovative solutions and translate them into business value and organizational capability.
  • Proven ability to build, develop, and lead high-performing teams through coaching, mentoring, succession planning, and organizational development.
  • Ability to engage effectively with senior leadership, regulatory agencies, external partners, and industry forums.

Responsibilities

  • Define and execute the long-term strategy, governance model, and roadmap for laboratory systems, digital technologies, data platforms, and analytical capabilities supporting Cell Therapy laboratory operations.
  • Establish strategic priorities that align technology investments with business objectives, regulatory requirements, and operational needs.
  • Serve as the technology and business leader for laboratory systems and digital capabilities across the Cell Therapy laboratory network.
  • Drive network-level decisions regarding laboratory digitalization, automation, data management, and systems integration.
  • Oversee lifecycle management, governance, enhancement, and expansion of GMP laboratory systems and technology platforms.
  • Ensure alignment, standardization, and harmonization of laboratory systems, processes, data standards, and business practices across sites and functions.
  • Partner with Quality, Manufacturing, Technical Operations, IT, Digital, Regulatory, and Supply Chain organizations to establish future-state capabilities and technology solutions.
  • Ensure laboratory systems remain inspection-ready, compliant, secure, and aligned with global regulatory expectations and data integrity requirements.
  • Sponsor strategic initiatives related to system modernization, automation, integration, analytics, and digital transformation.
  • Lead complex, high-impact initiatives that improve laboratory performance, compliance, efficiency, and business outcomes.
  • Identify and implement new technologies, advanced analytics, automation tools, and digital solutions to drive innovation.
  • Challenge existing processes and practices to deliver sustainable improvements and organizational transformation.
  • Establish metrics and governance processes to monitor system performance, user adoption, operational effectiveness, and business value realization.
  • Translate industry best practices and emerging technologies into strategic initiatives that strengthen Cell Therapy capabilities.
  • Lead cross-functional teams supporting large, complex, high-risk, or high-value initiatives across multiple sites and technology platforms.
  • Represent ASAT and Quality organizations in strategic governance forums, leadership reviews, inspections, and regulatory interactions.
  • Foster a culture of accountability, innovation, scientific excellence, inclusion, and continuous learning.
  • Mentor and serve as a role model, influencing culture, leadership behaviors, and technical excellence across teams and functions.

About the Company

Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Bristol Myers Squibb discovers, develops and sells prescription medicines for serious illnesses, including cancer, blood disorders, immune diseases and heart disease, for patients treated by doctors and hospitals around the world. Its best-known drug is Opdivo, an immunotherapy that helps the body's own immune system find and attack many kinds of cancer. Researchers develop drug candidates in its labs or bring them in through acquisitions and partnerships, then test them in clinical trials to win regulatory approval. The company makes and markets the approved medicines and earns its revenue from sales of patent-protected drugs. Its roots go back to a business founded in 1887, and it is based in Lawrence Township, New Jersey.

Company size
10,001+
Company stage
IPO
Headquarters
Lawrence Township, NJ
Founded
1887

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