Associate Director, Supply Chain Product Planning
Immunovant
August 14, 2026
Remote
United States
Operations
The Associate Director, Supply Chain Product Planning is responsible for integrated clinical and commercial product planning, including generating/updating the master production schedule across multiple global external CMOs; monitoring global stock levels; setting safety stock guidelines; tracking expirations; and allocating bulk materials.
Key Responsibilities:
- Develop and maintain combined clinical and commercial forecasts in SCMS planning/inventory tools.
- Translate clinical enrollment schedules and commercial sales forecasts into master production plans for drug substance, drug product, drug/device combination products, and clinical/commercial finished goods.
- Allocate drug substance batches to clinical vs. commercial end use (regulatory-driven requirements).
- Build and maintain item/material masters in SCMS.
- Provide supply chain input into CD&OP/S&OP.
- Request supplies from CMO core teams and integrate endorsed manufacturing schedules into master production plans.
- Generate/communicate bulk material allocations and finished goods production plans for packaging/labeling execution.
- Establish safety stock guidelines, project inventory positions, and prevent overstocking/stockouts.
- Monitor global stock, safety stock, and expiration dates.
- Develop scenarios for dynamic projections and communicate end-to-end material impacts.
- Partner with finance on budget impact of planning scenarios.
- Identify supply bottlenecks, manage lead times, maintain continuity under GxP.
- Support commercial launch readiness.
Requirements:
- Bachelor’s degree in biotechnology, life sciences, supply chain, business, engineering, or related field.
- 7+ years biopharmaceutical industry experience; 3+ years in production planning, inventory control, or demand forecasting for clinical and commercial materials.
- Experience with planning/forecasting/inventory management and ERP processes.
- Strong manufacturing process knowledge (drug substance/product, drug/device combinations, clinical & commercial finished goods).
- Very good cGMP and regulatory understanding for material releases and country requirements; strong cGMP/GDP knowledge.
- Proficiency with MS Office/Excel/SharePoint; strong communication, organization, relationship-building, problem-solving.
- Hands-on, high-urgency drive; ability to challenge status quo.
Work Environment/Travel:
- Remote-based; domestic/international travel (10–20%).
Compensation:
- Salary range: $170,000–$190,000 USD.
Key Responsibilities:
- Develop and maintain combined clinical and commercial forecasts in SCMS planning/inventory tools.
- Translate clinical enrollment schedules and commercial sales forecasts into master production plans for drug substance, drug product, drug/device combination products, and clinical/commercial finished goods.
- Allocate drug substance batches to clinical vs. commercial end use (regulatory-driven requirements).
- Build and maintain item/material masters in SCMS.
- Provide supply chain input into CD&OP/S&OP.
- Request supplies from CMO core teams and integrate endorsed manufacturing schedules into master production plans.
- Generate/communicate bulk material allocations and finished goods production plans for packaging/labeling execution.
- Establish safety stock guidelines, project inventory positions, and prevent overstocking/stockouts.
- Monitor global stock, safety stock, and expiration dates.
- Develop scenarios for dynamic projections and communicate end-to-end material impacts.
- Partner with finance on budget impact of planning scenarios.
- Identify supply bottlenecks, manage lead times, maintain continuity under GxP.
- Support commercial launch readiness.
Requirements:
- Bachelor’s degree in biotechnology, life sciences, supply chain, business, engineering, or related field.
- 7+ years biopharmaceutical industry experience; 3+ years in production planning, inventory control, or demand forecasting for clinical and commercial materials.
- Experience with planning/forecasting/inventory management and ERP processes.
- Strong manufacturing process knowledge (drug substance/product, drug/device combinations, clinical & commercial finished goods).
- Very good cGMP and regulatory understanding for material releases and country requirements; strong cGMP/GDP knowledge.
- Proficiency with MS Office/Excel/SharePoint; strong communication, organization, relationship-building, problem-solving.
- Hands-on, high-urgency drive; ability to challenge status quo.
Work Environment/Travel:
- Remote-based; domestic/international travel (10–20%).
Compensation:
- Salary range: $170,000–$190,000 USD.