
51 - 200 employees
Founded 2018
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
Healthcare • Biotechnology • Pharmaceuticals
Immunovant is a company focused on advancing treatments for autoimmune diseases through a patient-focused approach. With a vision of enabling normal lives for people with autoimmune diseases, Immunovant applies its expertise in science to develop and test new therapies. The company emphasizes complex and variable needs across different stages and severities of diseases. Immunovant is committed to pushing forward its therapeutic areas and clinical trials, while also engaging with patients, caregivers, and investors about their ongoing studies and corporate initiatives.
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51 - 200 employees
Founded 2018
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
Healthcare • Biotechnology • Pharmaceuticals
Immunovant is a company focused on advancing treatments for autoimmune diseases through a patient-focused approach. With a vision of enabling normal lives for people with autoimmune diseases, Immunovant applies its expertise in science to develop and test new therapies. The company emphasizes complex and variable needs across different stages and severities of diseases. Immunovant is committed to pushing forward its therapeutic areas and clinical trials, while also engaging with patients, caregivers, and investors about their ongoing studies and corporate initiatives.
• Develop and maintain combined clinical and commercial forecasts in the supply chain management system (SCMS) planning and inventory management tool • Translate clinical trial enrollment schedules and commercial sales forecasts into master production plans for drug substance, drug product, drug/device combination products, clinical finished goods, and commercial finished goods • Allocate drug substance batches to clinical versus commercial end use, considering Regulatory-driven material requirements • Build and maintain item/material masters within the SCMS tool • Contribute supply chain input to cross-functional CD&OP/S&OP processes • Provide supply plan requests to CMO core teams and integrate endorsed manufacturing schedules into the SCMS master production plan • Generate and communicate bulk material allocations and finished goods production plans to clinical and commercial supply colleagues • Establish safety stock guidelines, project future inventory positions, and prevent overstocking or stockouts • Monitor global stock levels, safety stock, and expiration dates • Develop and compare planning scenarios and communicate their end-to-end materials impact • Partner with finance to determine the budget impact of planning scenarios • Identify supply bottlenecks, manage lead times, and maintain operational continuity under strict GxP rules • Support commercial launch readiness activities
• Bachelor's degree in biotechnology, life sciences, supply chain, business, engineering, or another relevant field • 7+ years of relevant biopharmaceutical industry experience • 3+ years in production planning, inventory control, or demand forecasting for both clinical and commercial materials in biotech, pharmaceutical, or regulated life sciences sectors • Experience using multiple systems for planning, forecasting, inventory management, and ERP processes • Excellent understanding of manufacturing processes for drug substance, drug product, drug/device combination products, clinical finished goods, and commercial finished goods • Very good understanding of cGMP and Regulatory requirements for material releases, country requirements, and related areas • Strong computer skills, including MS Office, Excel, and SharePoint • Strong communication, problem-solving, and organization skills • Strong capability to build relationships across the organization and externally • Technical, operational, and business-oriented mindset capable of analyzing and resolving complex, multifaceted issues • Ability to challenge the status quo and think outside the box • Entrepreneurial spirit and dedication to delivering results • Desire to work in a fast-paced, dynamic, and innovative environment • Ability to collaborate on a cross-functional team • Strong working knowledge of cGMP and GDP requirements • Remote-based work environment • Domestic or international travel required (10–20%)
• Equity and other forms of compensation may be provided as part of a total compensation package • Medical benefits • Dental benefits • Vision benefits • 401(k) • Unlimited paid time off • Parental leave
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