Manager of Site Supply Planning and Scheduling
Regeneron
August 13, 2026
On-site
East Greenbush, NY
Operations
Discover Your Role
- Oversee the creation and execution of the site master production schedule to ensure reliable supply of clinical and commercial products based on demand forecasts, program strategies, and operational capabilities.
- Act as the planning liaison for site teams, reflecting manufacturing capabilities, constraints, and performance; proactively identify and resolve conflicts.
- Lead finite scheduling for production and post-production activities, coordinating with external departments for maintenance, cleaning, validation, and microbial monitoring.
- Steward produced batches through post-production milestones, tracking batch statuses and mitigating risks to downstream supply nodes.
- Lead scenario-based planning and risk assessments; implement business continuity plans to ensure uninterrupted supply.
- Manage capacity project portfolio, recommending capital expenditures and aligning implementation with program, regulatory, and supply strategies.
- Implement real-time monitoring systems for schedule adherence; improve communication to and from the production floor.
- Champion continuous improvement to reduce lead times, manage costs, and enhance operational efficiency.
This Role Requires
- Bachelor’s degree in Business, Engineering, Supply Chain Management, or related field.
- Associate Manager: 6+ years; Manager: 7+ years in supply chain, manufacturing, or operations planning within biotech, pharmaceutical, or life sciences.
- End-to-end planning experience in a cGMP manufacturing environment with strong regulatory understanding.
- Expertise in production planning, capacity planning, and supply chain concepts; ERP/MRP/APS and project management systems experience a plus.
- Track record managing complex cross-functional projects/portfolios; PMP, APICS, or Lean Six Sigma a plus.
Application instructions
- “Apply now.”
- Oversee the creation and execution of the site master production schedule to ensure reliable supply of clinical and commercial products based on demand forecasts, program strategies, and operational capabilities.
- Act as the planning liaison for site teams, reflecting manufacturing capabilities, constraints, and performance; proactively identify and resolve conflicts.
- Lead finite scheduling for production and post-production activities, coordinating with external departments for maintenance, cleaning, validation, and microbial monitoring.
- Steward produced batches through post-production milestones, tracking batch statuses and mitigating risks to downstream supply nodes.
- Lead scenario-based planning and risk assessments; implement business continuity plans to ensure uninterrupted supply.
- Manage capacity project portfolio, recommending capital expenditures and aligning implementation with program, regulatory, and supply strategies.
- Implement real-time monitoring systems for schedule adherence; improve communication to and from the production floor.
- Champion continuous improvement to reduce lead times, manage costs, and enhance operational efficiency.
This Role Requires
- Bachelor’s degree in Business, Engineering, Supply Chain Management, or related field.
- Associate Manager: 6+ years; Manager: 7+ years in supply chain, manufacturing, or operations planning within biotech, pharmaceutical, or life sciences.
- End-to-end planning experience in a cGMP manufacturing environment with strong regulatory understanding.
- Expertise in production planning, capacity planning, and supply chain concepts; ERP/MRP/APS and project management systems experience a plus.
- Track record managing complex cross-functional projects/portfolios; PMP, APICS, or Lean Six Sigma a plus.
Application instructions
- “Apply now.”