Manufacturing Production Scheduler & Process Optimization Specialist

Sanofi•Pearl River, NY

3d•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.

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