Associate Director - Supply Chain

Lilly • Philadelphia, PA

4d • $127,500 - $187,000 • Hybrid

About The Position

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Position Overview:
The Associate Director, Supply Chain will lead and grow a supply chain team responsible for ensuring supply continuity of all critical components and consumables required for the uninterrupted manufacturing of commercial and clinical radiopharmaceutical drug products across a worldwide network of cGMP manufacturing sites. Key focus areas include optimizing the global supply chain, maintaining approved suppliers/products for global operations, demand/supply/capacity planning, sourcing, labeling, dispensing, inventory management, shipping, distribution, and selection of drug supply-related vendors and depots.

Requirements

• Earned Bachelor's degree in supply chain, science/engineering, production operations management, business, or related field
• 5+ years of experience in a supply chain function within a pharmaceutical environment
• 2+ years of CMC experience in the biotechnology or pharmaceutical development industries
• Strong supply management expertise, including a combination of experiences with forecasting, demand/supply planning, IRT systems, inventory management/ERP systems, clinical labeling, distribution including cold chain, import/export, reverse logistics, CMC and/or GxP regulations
• Excellent interpersonal, verbal, and written communication skills
• Ability to work with uncertainty and shifting priorities, and to resolve conflict in a constructive manner
• Must be self-motivated and comfortable in a fast-paced, demanding and dynamic work environment
• Must be proficient in the Microsoft 365 environment

Nice To Haves

• Earned Master's degree in a relevant field
• Familiarity with cGMPs as well as US, European, Japanese, Chinese, and ICH regulations and industry standards for pharmaceutical manufacturing
• Previous project management or project leadership
• Experience within a CMC/cGMP role in the radiopharmaceutical industry
• Familiarity with collaborative project management tools such as Microsoft Project, Smartsheet, Monday, Jira, etc.
• Solid understanding of pharmaceutical manufacturing and release within a cGMP environment
• Supply Chain Management certification(s) (e.g., CSCP, CPIM, SCOR-P, CPM, etc.)

Responsibilities

• Ensure uninterrupted supply of critical components and consumables to meet global manufacturing needs for commercial and clinical products
• Evaluate and communicate risks and interruptions to the supply chain and proactively establish mitigations wherever necessary
• Partner closely with Commercial, Clinical, Manufacturing, and Leadership teams to establish and maintain robust supply/demand forecasts in alignment with core business goals
• Build, deploy, and maintain tools for cross-functional tracking and communication of approved suppliers, products, and components
• Review technical and regulatory documentation to ensure accuracy, consistency, and currency of all critical components/key consumables
• Support management and closure of product investigations associated with critical components/key consumables including authoring and reviewing investigation documents and risk assessments
• Track component recalls/retrievals and communicate cross-functionally as necessary
• Identify alternative component sources; manage associated change control process where needed
• Manage financial planning and budget forecasting activities associated with the supply chain function; perform invoice reconciliation, ensure functional area adherence to budget
• Prepare and present supply chain updates at regular internal work group and team meetings; support the preparation of presentation materials for senior leadership, when required.
• Assume additional responsibilities supporting the broader CMC Development group, as needed.

Benefits

• company bonus (depending, in part, on company and individual performance)
• company-sponsored 401(k)
• pension
• vacation benefits
• medical, dental, vision and prescription drug benefits
• flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
• life insurance and death benefits
• certain time off and leave of absence benefits
• well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)

What This Job Offers

• Job Type: Full-time
• Career Level: Manager