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Director, QC Automation

$197.47k - $239.29k

Bristol Myers Squibb

Bristol Myers Squibb seeks a Director to own the deployment and lifecycle of automated quality control systems across cell therapy manufacturing sites. This role coordinates multi-program priorities, manages vendor relationships, and ensures regulatory compliance while leading cross-functional teams.

Responsibilities

  • Own technology roadmap and lifecycle for automated QC equipment and software, including vendor management
  • Lead deployment of automated QC systems across cell therapy manufacturing network nodes
  • Partner with assay automation and analytical sciences teams to define requirements and resolve issues
  • Serve as primary contact for receiving sites, ensuring operational and quality readiness
  • Identify deployment risks and drive mitigation plans; ensure cGMP compliance

Requirements

  • 12+ years experience in regulated pharmaceutical or biotech manufacturing
  • 5+ years leading technology deployment, automation, or tech transfer projects
  • In-depth knowledge of cGMP and pharmaceutical regulations
  • Experience with automated lab or analytical technologies
  • Proven cross-functional team leadership and competing priority coordination
  • Strong stakeholder management and influencing skills in matrix organizations
  • Solid problem-solving and risk-mitigation capabilities

Compensation: $184,550 - $245,995 base depending on location

Vacancy posted 13 days ago
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