Fujifilm-posted 12 days ago
Holly Springs, NC

The Production Scheduler, Drug Product Finished Goods is responsible for creating, maintaining, and optimizing daily and long-term production schedules across drug product manufacturing, filling, inspection, and packaging operations. This role ensures timely product delivery and efficient use of resources while adhering to current Good Manufacturing Practices (cGMP). Acting as a central coordination point, the scheduler partners with other departments (e.g., Manufacturing, Planning, Quality, Supply Chain) to align material availability, equipment capacity, and staffing needs with the production plan.

  • Develops and manages detailed production schedules based on demand forecasts, inventory goals, and equipment and labor capacity
  • Collaborates with cross-functional teams (e.g., Manufacturing, Planning, Quality, Supply Chain, Facilities, Warehouse) to align production activities and meet operational objectives
  • Monitors execution of production schedules and makes proactive adjustments in response to delays, equipment issues, or deviations
  • Communicates schedule updates, challenges, and risks clearly and promptly to stakeholders
  • Coordinates with materials management to confirm availability of raw materials and components needed for production
  • Contributes to long-term capacity planning and resource forecasting in support of strategic business initiatives
  • Utilizes enterprise systems (Enterprise Resource Planning [ERP]/Manufacturing Execution System [MES]) to issue work orders, monitor progress, and track key performance metrics
  • Participates in daily and weekly planning meetings to support real-time operational decisions
  • High school diploma with 8+ years related experience OR
  • Associate’s Degree in Life or Pharmaceutical Sciences, Biotechnology, Microbiology, or a related field with 6+ years of direct experience OR
  • Bachelor’s in Life or Pharmaceutical Sciences, Biotechnology, Microbiology, or a related field with 4+ years of direct experience
  • Equivalent military experience or training
  • Experience in drug product manufacturing, sterile processing, or quality assurance
  • Proficiency in ERP systems (e.g., SAP, Oracle) and MES platforms (e.g., PAS-X)
  • BioWorks or BTEC coursework
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service