Director, Supply Chain Product Planning

🕒 il y a 1 jour

🇺🇸 États-Unis – Télétravail

💵 $200 000 - $235 000 / an

⏰ Temps Plein

🔴 Expert

🔗 Responsable Supply Chain

🗣️🇺🇸🇬🇧 Anglais requis

D'où vient cette offre

Publiée sur la page carrières de Immunovant, pas via un site d'emploi

Repérée par Remote Rocketship il y a 1 jour

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Immunovant

51 - 200 employés

Fondée en 2018

🏥 Santé

🧬 Biotechnologie

💊 Pharmaceutique

Healthcare • Biotechnology • Pharmaceuticals

Immunovant est une entreprise dédiée à l'avancement des traitements pour les maladies auto-immunes grâce à une approche centrée sur le patient. Avec pour vision de permettre une vie normale aux personnes atteintes de maladies auto-immunes, Immunovant utilise son expertise scientifique pour développer et tester de nouvelles thérapies. L'entreprise met l'accent sur les besoins complexes et variés à travers les différents stades et degrés de gravité des maladies. Immunovant s'engage à faire progresser ses domaines thérapeutiques et ses essais cliniques, tout en dialoguant avec les patients, les aidants et les investisseurs au sujet de leurs études en cours et de leurs initiatives d'entreprise.

Description

• Develop and maintain combined clinical and commercial forecasts in the SCMS planning and inventory management tool • Track forecast accuracy • Translate clinical trial enrollment schedules and commercial sales forecasts into master production plans • Allocate drug substance batches to clinical and commercial end use • Communicate bulk material allocations and finished goods production plans to supply colleagues and vendors • Build and maintain item/material masters and help define master data standards • Contribute supply chain input to cross-functional CD&OP/S&OP processes • Provide supply plan requests to CMO core teams and integrate manufacturing schedules into the master production plan • Establish safety stock, lot sizing, shelf-life, and expiry policies • Project inventory positions and monitor global stock levels, safety stock, and expiration dates • Plan material requirements against bills of materials and CMO schedules • Develop scenarios and communicate end-to-end material and budget impacts with Finance • Identify supply bottlenecks, manage lead times, and maintain operational continuity under GxP rules • Support commercial launch readiness • Develop, document, and implement forecasting, S&OP, master production scheduling, materials planning, inventory management, and allocation processes • Define requirements, configure, test, validate, and train users on ERP and SCMS planning processes • Support evaluation and selection of ERP, SCMS, planning, and analytics tools • Build dashboards, reports, and models from ERP and SCMS data • Define and track planning KPIs including forecast accuracy, plan adherence, CMO schedule adherence, inventory days on hand, and expiry/write-off rates • Collaborate with clinical supply chain, commercial supply chain, CMC project management, CMC-QA, Finance, IT, QA, and external CMO partners

🎯 Exigences

• Bachelor's degree in biotechnology, life sciences, supply chain, business, engineering or another relevant field • 10+ years of relevant biopharmaceutical industry experience • 7+ years in production planning, inventory control, or demand forecasting for both clinical and commercial materials within biotech, pharmaceutical, or regulated life sciences sectors • Hands-on expertise with ERP, SCMS, and planning systems for planning, forecasting, inventory management, and materials requirements planning • Deep expertise in demand, supply, and materials planning, including S&OP, master production scheduling, MRP, safety stock and inventory optimization, and scenario planning • Experience designing planning processes within and outside ERP and SCMS tools and implementing them in systems, including testing, validation, and change management • Experience contributing to system evaluation and selection • Strong data analytics skills, including advanced Excel, SQL, and BI tools such as Power BI and Tableau • Ability to present analyses and recommendations to senior leadership and work effectively with external CMO and vendor partners • Understanding of manufacturing processes for drug substance, drug product, drug/device combination products, clinical finished goods, and commercial finished goods • Working knowledge of cGMP, GDP, and regulatory requirements • Strong computer skills including MS Office, Excel, and SharePoint • Strong communication, problem-solving, organization, relationship-building, and cross-functional collaboration skills • Ability to work in a fast-paced, dynamic, and innovative environment • Domestic or international travel required (10–20%) • Advanced degree and/or APICS CPIM/CSCP certification preferred

🏖️ Avantages

• Equity and other forms of compensation may be provided as part of a total compensation package • Medical benefits • Dental benefits • Vision benefits • 401k • Unlimited paid time off • Parental leave • Remote-based work environment

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