
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.
🔥 14 hours ago
🇺🇸 United States – Remote
💵 $66k - $169.4k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
✅ Product Manager
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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.
• Serve as Product Quality Lead for assigned programs • Investigate and finalize reporting activities for potential product complaints • Support Clinical Operations in evaluating product temperature excursions • Support manufacturing campaigns and release activities • Ensure archival and expedient retrieval of key manufacturing documentation • Review deviations, investigations, CAPAs, and change controls for adequacy • Analyze and report product quality trends • Facilitate risk assessments and mitigation activities • Perform routine risk monitoring activities • Partner with Technical Operations, Supply Chain, Regulatory Affairs, and Manufacturing teams to support regulatory submissions • Support inspections and audits
• BS/MS in Life Sciences • 5-10 years pharmaceutical quality experience • Knowledge of GMP manufacturing and quality systems • Adaptive problem solver • Technical depth and a growth mindset • Curiosity and drive for self-identified innovation, especially in artificial intelligence and digital
• 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 • Time off and leave of absence benefits • Employee assistance program • Fitness benefits • Employee clubs and activities
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