Deputy Director Manufacturing Operations

Job Description:

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Job Title: Deputy Director Manufacturing Operations

Location: Pearl River, NY

About the Job

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

About Sanofi:

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.

Main Responsibilities

Leadership & Team Management

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

Manufacturing Readiness & Operations

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

Quality, Compliance & Continuous Improvement

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

Strategic & Cross-Functional Collaboration

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 timely manner

Support the development and management of departmental budgets and resource planning

About You

Basic Qualifications

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 implement effective corrective actions.

Experience with performance management routines, including +QDCI or equivalent operational excellence frameworks.

Strong conflict management skills with the ability to navigate interpersonal and team dynamics effectively.

Demonstrated sense of urgency and ability to prioritize and respond decisively in a fast-paced manufacturing environment

Excellent communication, organizational, and stakeholder management skills

Understanding of cell growth and propagation principles as they apply to biopharmaceutical drug substance manufacturing

Preferred Qualifications

Advanced degree (MS, MBA) in Life Sciences, Engineering, Business Administration or related technical field.

Hands-on experience with one or more of the following technologies:

Single Use Systems

Chromatography

Tangential Flow Filtration

Stainless Steel Systems (Fermenters and Bioreactors)

Why choose us?

Bring the miracles of science to life alongside a supportive, future-focused team.

Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.

Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.

Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.

Power industry-leading performance by leveraging digital, data, and AI-driven innovation – at speed and scale

Transform lives worldwide by delivering life-changing treatments anywhere, anytime.

Sanofi US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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All compensation will be determined commensurate with demonstrated experience. xhyhwjd Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.