Deputy Director Manufacturing Operations

Job Title
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Deputy Director Manufacturing Operations

Location: Pearl River, NY

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and  Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s 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.

• 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 elevate risks to manufacturing readiness, supply continuity, or compliance in a timely manner

• Support the development and management of departmental budgets and resource planning

• Bachelor’s degree in engineering, Science, Life Sciences, Business, or any related field.

• 5
  -7 years of experience in pharmaceutical or biopharmaceutical manufacturing.

• 5+ years of Progressive, hands‑on leadership experience in a GMP manufacturing environment, with an expectation to interact with and solve problems at the shop floor level.

• Strong working knowledge of GMP and GDP regulations and their application in a manufacturing environment

• Proven expertise in Lean manufacturing methodologies (5s, Gemba Problem Solving, Daily Capacity Management) and defect identification/reduction.

• Demonstrated ability to perform thorough root cause analysis on manufacturing deviations and…