Director, Integrated Demand and Supply Planning

Role Summary

Director, Integrated Demand and Supply Planning

Join Immatics to lead site planning, master production scheduling, and end-to-end planning processes across Supply Chain, Manufacturing, Clinical, and Development to support clinical and commercial operations. Oversee ERP/digital system implementations and ensure robust capacity forecasting and inventory management in a regulated environment.

Responsibilities

• Act as the main point of contact for communication and coordination between Supply Chain, Manufacturing, Clinical, and Development teams to ensure accurate demand planning, material forecasting, and capacity management.
• Develop, implement, and manage a robust Master Production Schedule (MPS) aligned with demand forecasts, capacity constraints, material availability, and quality timelines.
• Lead Sales & Operations Planning (S&OP) processes at site and global levels, incorporating tactical and strategic horizons.
• Collaborate with cross-functional teams to ensure a feasible and optimized integrated site operational plan.
• Create and maintain scenario planning tools to assess impacts of changes in demand, supply interruptions, or constraints.
• Serve as the site planning SME during internal and external audits, inspections, and cross-functional meetings.
• Partner with IT/Systems teams to optimize planning tools and SAP modules; support material planning and inventory management initiatives; lead or support digital transformation projects.
• Mentor and develop planning capabilities in adjacent teams; assist in budget and headcount forecasting based on production scenarios.

Qualifications

• Bachelor‚Äôs degree in Supply Chain Management, Business Administration, Engineering, or related field (or equivalent).
• 5+ years of direct SAP experience in Plan to Produce and/or Materials Management Modules; strong ERP/MRP proficiency (e.g., SAP, Oracle, NetSuite) and advanced Excel.
• Deep understanding of production planning, inventory management, and supply chain dynamics; experience in clinical or commercial manufacturing, especially cell or gene therapy.
• Experience developing and managing a Master Production Schedule in a dynamic, regulated environment.
• Excellent interpersonal and communication skills with ability to influence cross-functional stakeholders.

Preferred Qualifications

• ERP implementation experience.
• APICS CPIM or similar certification.
• Experience with early-stage commercialization or new product introduction in biotech.
• Knowledge of cell therapy process flows, including scheduling, cleanroom constraints, and QC release.

Skills

• Strategic Thinking
• Executional Rigor
• Problem Solving
• Cross-functional Collaboration
• Adaptability
• Leadership
• Strong written and verbal communication
• Ability to follow CFR/OSHA/GMP procedures

Education

• Bachelor‚Äôs degree in a relevant field (or equivalent experience)

Additional Requirements

• On-site role in Stafford, TX; 8:00 AM ‚Äì 5:00 PM; may require work in cleanrooms and labs with PPE as needed.
• Legal eligibility to work in the United States; E-Verify participation