Manufacturing Production Scheduler & Process Optimization Specialist
Sanofi•Pearl River, NY
•$78,000 - $112,667•Onsite
About The Position
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. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Requirements
- Bachelor's degree in engineering, Business or related field
- 1+ years of experience in manufacturing processes and production planning principles.
- Knowledge of Lean Manufacturing methodologies and continuous improvement tools
- Familiarity with GMP/GDP requirements in pharmaceutical manufacturing
- Excellent analytical and problem-solving skills
- Strong communication and collaboration abilities
- Proficiency in data analysis and manufacturing systems (MES, ERP)
Nice To Haves
- Master's Degree or MBA
- Previous internship or experience in pharmaceutical manufacturing
- Experience with SMS tools and visual management systems
- Knowledge of capacity planning and scheduling software
- Understanding of regulatory compliance in pharmaceutical operations
Responsibilities
- 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
- 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
- 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
- Serve as backup support for Manufacturing Managers during absences
- Participate in daily management routines and escalation processes
- Support decision-making processes and operational troubleshooting
- 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
Benefits
- high-quality healthcare
- prevention and wellness programs
- at least 14 weeks’ gender-neutral parental leave
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
