Associate Director, Supply Chain Product Planning
Immunovant
August 14, 2026
Remote
United States
Operations
The Role
Reporting to the Senior Director, Global Supply Chain and Logistics, the Associate Director, Supply Chain Product Planning is responsible for integrated clinical and commercial product planning. Responsibilities include 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 based on actual demands and future inputs.
- Translate clinical trial 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, considering regulatory-driven material requirements.
- Build and maintain item/material masters in SCMS.
- Provide supply chain input into CD&OP/S&OP processes.
- Submit supply plan requests to CMO core teams and integrate endorsed manufacturing schedules into the master production plan.
- Generate and communicate bulk material allocations and finished goods production plans to support packaging/labeling execution.
- Establish safety stock guidelines; project inventory positions; prevent overstocking/stockouts.
- Monitor global stock, safety stock, and expiration dates.
- Model scenarios for changing clinical/commercial projections and communicate end-to-end material impacts.
- Partner with finance on budget impact of planning scenarios.
- Identify supply bottlenecks, manage lead times, and maintain operational 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 production planning, inventory control, or demand forecasting for clinical and commercial regulated materials.
- Experience with planning/forecasting/inventory systems and ERP processes.
- Strong understanding of manufacturing processes for drug substance, drug product, drug/device combinations, and clinical/commercial finished goods.
- Very good understanding of cGMP and regulatory requirements for material releases and country requirements.
- Strong computer skills (MS Office, Excel, SharePoint, etc.).
- Hands-on, urgent, results-driven, strong communicator/problem-solver, highly organized.
- Ability to build internal/external relationships; analyze and resolve complex issues.
- Ability to challenge the status quo; entrepreneurial, collaborative.
- Strong working knowledge of cGMP and GDP.
- Remote-based; domestic/international travel 10–20%.
Salary range: $170,000 USD - $190,000 USD.
Reporting to the Senior Director, Global Supply Chain and Logistics, the Associate Director, Supply Chain Product Planning is responsible for integrated clinical and commercial product planning. Responsibilities include 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 based on actual demands and future inputs.
- Translate clinical trial 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, considering regulatory-driven material requirements.
- Build and maintain item/material masters in SCMS.
- Provide supply chain input into CD&OP/S&OP processes.
- Submit supply plan requests to CMO core teams and integrate endorsed manufacturing schedules into the master production plan.
- Generate and communicate bulk material allocations and finished goods production plans to support packaging/labeling execution.
- Establish safety stock guidelines; project inventory positions; prevent overstocking/stockouts.
- Monitor global stock, safety stock, and expiration dates.
- Model scenarios for changing clinical/commercial projections and communicate end-to-end material impacts.
- Partner with finance on budget impact of planning scenarios.
- Identify supply bottlenecks, manage lead times, and maintain operational 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 production planning, inventory control, or demand forecasting for clinical and commercial regulated materials.
- Experience with planning/forecasting/inventory systems and ERP processes.
- Strong understanding of manufacturing processes for drug substance, drug product, drug/device combinations, and clinical/commercial finished goods.
- Very good understanding of cGMP and regulatory requirements for material releases and country requirements.
- Strong computer skills (MS Office, Excel, SharePoint, etc.).
- Hands-on, urgent, results-driven, strong communicator/problem-solver, highly organized.
- Ability to build internal/external relationships; analyze and resolve complex issues.
- Ability to challenge the status quo; entrepreneurial, collaborative.
- Strong working knowledge of cGMP and GDP.
- Remote-based; domestic/international travel 10–20%.
Salary range: $170,000 USD - $190,000 USD.