Manufacturing Production Scheduler & Process Optimization Specialist

Job Title: Manufacturing Production Scheduler & Process Optimization Specialist Location: Pearl River, NY About the Job We are seeking a dynamic Industrial Engineering professional to join our manufacturing team as a Manufacturing Production Scheduler & Process Optimization Specialist. This L2-1 role is ideal for someone who is passionate about optimizing manufacturing operations while ensuring compliance with pharmaceutical industry standards. About Sanofi We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Main Responsibilities Production Planning & Scheduling Build, plan, and optimize manufacturing production schedules to maximize efficiency and meet delivery commitments Coordinate with cross-functional teams to ensure seamless production flow and capacity utilization Manage daily capacity planning and resource allocation across manufacturing operations Lean Manufacturing & SMS Implementation Drive implementation and continuous improvement of Lean Manufacturing principles and SMS (Sanofi Manufacturing System) 2.0 tools and practices Lead 5S initiatives and workplace organization programs Facilitate Gemba walks and problem‑solving sessions to identify and eliminate waste Support visual management systems and standard work documentation Process Optimization & Continuous Improvement Analyze production data to identify bottlenecks, inefficiencies, and improvement opportunities Lead cross-functional problem‑solving initiatives using structured methodologies Support process improvements and optimization projects to enhance productivity and quality Leadership Support & Backup Serve as backup support for Manufacturing Managers during absences Participate in daily management routines and escalation processes Support decision‑making processes and operational troubleshooting Regulatory & Compliance Requirements Ensure all activities comply with Good Manufacturing Practices (GMP) guidelines and pharmaceutical quality standards Maintain adherence to Good Documentation Practices (GDP) where applicable Support regulatory inspections and compliance audits Follow all Health, Safety, and Environmental (HSE) regulations and procedures Maintain accurate documentation and batch records in accordance with cGMP requirements About You Basic Qualifications Bachelor's degree in engineering, Business or related field 1+ years of experience in manufacturing processes and production planning principles. Technical Skills Knowledge of Lean Manufacturing methodologies and continuous improvement tools Familiarity with GMP/GDP requirements in pharmaceutical manufacturing Soft Skills Excellent analytical and problem‑solving skills Strong communication and collaboration abilities Proficiency in data analysis and manufacturing systems (MES, ERP) Proficiency in data analysis and manufacturing systems (MES, ERP) Preferred Qualifications Master's Degree or MBA Previous internship or experience in pharmaceutical manufacturingExperience with SMS tools and visual management systems Knowledge of capacity planning and scheduling software Understanding of regulatory compliance in pharmaceutical operations 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 Inc. and its U.S. affiliates are Equal Opportunity and Affative Action employers committed to a culturally diverse 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. 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. #J-18808-Ljbffr Sanofi