Deputy Director Manufacturing Operations

Sanofi

Pearl River (NY)

On-site

USD 134,000 - 193,000

Full time

2 days ago
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Benefits offered by this job

14+ weeks parental leave
Health and wellbeing programs
Competitive compensation

Job summary

Sanofi Pearl River site in New York is seeking a Deputy Director of Manufacturing Operations to lead safe, compliant, and high-performing production activities. This role oversees upstream and downstream operations, drives readiness for scheduled production, and partners with QA, Regulatory Affairs, and cross-functional teams.

We expect 5+ years of GMP leadership, strong Lean and RCA experience, and excellent communication to foster accountability and continuous improvement in a fast-paced

Qualifications

  • Bachelor’s degree in engineering, science, life sciences, business or related field.
  • 7+ years in pharmaceutical/biopharmaceutical manufacturing.
  • 5+ years of progressive, hands-on leadership in GMP manufacturing.
  • Strong GMP/GDP knowledge and application.
  • Lean manufacturing knowledge including 5S and RCA.
  • Experience with performance management routines (+QDCI).
  • Strong communication and stakeholder management skills.

Responsibilities

  • Lead manufacturing readiness and oversee upstream/downstream processes (cell culture, protein production, purification).
  • Direct manufacturing teams to achieve output targets while ensuring quality and compliance.
  • Drive Lean initiatives to reduce waste and improve process efficiency.
  • Support inspections, audits, and regulatory submissions with QA and RA.

Skills

Leadership
GMP knowledge
Lean manufacturing
Root cause analysis
Quality systems
Cross-functional collaboration
Communication

Education

Bachelor's degree in engineering or life sciences

Tools

Single Use Systems
Chromatography
Tangential flow filtration
Fermenters/Bioreactors

Job description

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 elevate 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.
  • 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
  • Previous experience leading Managers or Supervisors is highly desired.
  • 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 andwellness 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 Inc. 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; colour; 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.

Sanofi US endeavours to make our career center accessible to any and all users. US and Puerto Rico Residents Only Sanofi Inc. 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. North America Applicants Only The salary range for this position is: $133.500,00 - $192.833,33 All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here. We are an R&D driven, AI-powered biopharma company committed to improving people’s lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people’s lives. We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world. Discover more about us visiting www.sanofi.com or via our movie We are Sanofi Start a career that makes a difference. Reinvention is in our DNA. It’s what drove our evolution from a small French enterprise to one of the world’s leading biopharma companies. Whether it’s using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities. This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people’s lives.

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