Jobs · Information Technology · New York

Deputy Director Manufacturing Operations

BioSpace · Pearl River, NY · 3 wk ago
Information TechnologyFull-time

About the role

Join a global network that powers how Sanofi delivers seamlessly, purposefully, and at scale. In Manufacturing & Supply, youll help reimagine how life-changing treatments reach people everywhere, faster. Sanofi is an R&D-driven, AI-powered biopharma company committed to improving peoples lives and delivering compelling growth. Our deep understanding of the immune system and innovative pipeline enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve lives.

Responsibilities

  • Ensure all areas and employees are safe at all times
  • Directly manage manufacturing teams supporting upstream and downstream Flublok drug substance operations
  • Foster a high-performance culture grounded in accountability, collaboration, and continuous improvement
  • Provide coaching, mentorship, and professional development to team members at all levels
  • Effectively manage conflict within and across teams to maintain a productive and respectful work environment
  • Drive a strong sense of urgency in day-to-day operations while maintaining quality and compliance standards
  • Ensure manufacturing areas are consistently ready for scheduled production activities
  • Oversee upstream and downstream manufacturing processes, including cell culture, protein production, clarification, purification, and related unit operations
  • Monitor and manage production schedules to meet output targets while maintaining compliance with all applicable standards
  • Ensure all equipment, materials, documentation, and personnel are in a state of readiness prior to manufacturing execution
  • Ensure all manufacturing activities are conducted in strict accordance with GMP (Good Manufacturing Practice) and GDP (Good Documentation Practice) requirements
  • Lead and support deviation investigations, applying structured root cause analysis (RCA) methodologies to identify, document, and resolve manufacturing deviations
  • Champion Lean manufacturing principles and defect identification practices to eliminate waste and drive process efficiency
  • Implement and sustain performance management routines, including +QDCI (Quality, Delivery, Cost, Involvement) metrics and visual management tools
  • Partner with Quality Assurance and Regulatory Affairs to support inspections, audits, and regulatory submissions as needed
  • Collaborate with Process Development, Quality, Supply Chain, and Engineering teams to support technology transfers, process improvements, and capacity planning
  • Represent manufacturing in cross-functional forums and contribute to site-level strategic initiatives
  • Identify and escalate risks to manufacturing readiness, supply continuity, or compliance in a

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