Associate Director, Supply Chain

🔥 45 minutes ago

🇺🇸 United States – Remote

💵 $117k - $189.2k / year

⏰ Full Time

🟠 Senior

🔗 Supply Chain

👻 Ghost score 0%

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Logo of Eli Lilly and Company

Eli Lilly and Company

10,000+ employees

💊 Pharmaceuticals

🏥 Healthcare

🧬 Biotechnology

💰 $6.5M Post-IPO Debt - Eli Lilly on 2024-02

Pharmaceuticals • Healthcare • Biotechnology

Eli Lilly and Company is a multinational pharmaceutical company that researches, develops, manufactures, and markets prescription medicines across multiple therapeutic areas including diabetes, oncology, immunology, neuroscience, and pain. Headquartered in Indianapolis, Indiana, Lilly is known for its extensive R&D, clinical development, and global commercialization of biologic and small-molecule drugs. The company focuses on drug discovery, clinical trials, regulatory approvals, and large-scale pharmaceutical manufacturing and distribution.

📋 Description

• Develop and implement strategies to deliver Investigational Product in support of several clinical programs • Report to the Senior Director, Clinical Supply Chain • Develop collaborative relationships with internal departments and third-party procurement, packaging, and distribution providers • Develop and maintain clinical forecasts, inventory databases and IRT systems • Provide daily oversight of clinical supplies • Develop and update clinical supply strategies to meet corporate demands • Identify supply chain risks and develop and implement mitigation strategies • Manage study/program budgets, contracts, change orders and spending • Develop and regularly update forecast/demand plans for late-phase clinical trials • Collaborate with Quality, Clinical, CMC and external CDMOs to develop and approve clinical labels • Manage CDMO packaging and labeling schedules • Manage logistics and licenses required to ship materials to bulk storage facilities, courier depots and investigator sites • Facilitate document transfer required for IP/QP release by CDMOs • Manage and track clinical supply inventory manually or through an IRT system • Manage product recovery pending investigation of IP from investigator sites • Monitor shelf life and expiry dating and coordinate retest extensions • Manage investigations, reporting and communication of temperature excursions and product complaints • Author or review supply chain sections of regulatory submissions • Participate as SME in CDMO audits or for-cause inspections when required • Contribute as an SME to CDMO selection and approval and review related MSAs and Quality Agreements • Represent Supply Chain in Clinical and CMC Sub Team meetings • Travel domestically and internationally as required

🎯 Requirements

• Bachelor’s degree in engineering or science is required • 7+ years of biotech/pharma industry experience in clinical supply with significant international experience is required • Experience in all aspects of clinical supply chain • Deep understanding of GMP/GDP • Strong understanding of managing groups, CMOs, CDMOs and other CDMOs • Strong organizational, analytical, decision-making and interpersonal skills • Ability to work on multiple projects independently in a fast-paced dynamic environment • Demonstrated ability to coordinate CDMO activities in the development and commercialization of pharmaceutical products • Excellent organizational skills, project management skills and detail-oriented leadership approach • Willing and able to travel both domestically and internationally

🏖️ 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 • 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, including employee assistance program, fitness benefits, and employee clubs and activities

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