
10,000+ employees
đź’Š Pharmaceuticals
🏥 Healthcare
🧬 Biotechnology
đź’° $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.
🔥 17 hours ago
🇺🇸 United States – Remote
đź’µ $129k - $231k / year
⏰ Full Time
đźź Senior
đź‘” Director
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10,000+ employees
đź’Š Pharmaceuticals
🏥 Healthcare
🧬 Biotechnology
đź’° $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.
• Manage and guide external vendors, including CROs and CDMOs • Execute physicochemical characterization and pre-formulation studies for New Chemical Entities (NCEs) • Design and develop nonclinical oral, subcutaneous, and intravenous formulations for stability, bioavailability, and effective drug delivery in animal models • Design and oversee nonclinical formulation stability and compatibility studies • Support clinical formulation development of oral solid dosage forms as needed • Author, review, and approve development and dose preparation protocols and reports • Review formulation-related sections of PK, PD, and safety study protocols and reports • Represent CMC and provide nonclinical formulation, DS and DP stability, and supply guidance at cross-functional team meetings • Coordinate shipments supporting nonclinical and clinical development supply requirements to CDMO and CRO sites • Assist with formulation-related documentation for regulatory submissions such as INDs and CTAs • Collaborate with discovery, nonclinical, clinical, project management, legal, sourcing, supply chain, quality, regulatory, and other CMC functions • Travel occasionally to domestic and international vendors
• BS or MS in Pharmaceutical Sciences or a related scientific discipline required • 7+ years of experience in small molecule formulation development, including support of nonclinical and clinical programs across oral, subcutaneous, and intravenous dosage forms • Deep understanding of formulation development and manufacturing of poorly soluble (BCS Class II/IV) small molecule compounds for oral, subcutaneous, and intravenous delivery • Strong knowledge of pharmaceutical and engineering principles related to liquid and solid dosage form development at clinical and commercial scale • Proficiency with analytical and solid-state characterization techniques, including HPLC/UPLC, XRPD, DSC, TGA, DVS, and related methodologies • Experience managing external development partners (CROs, CDMOs, CMOs) and coordinating pharmaceutical product development activities • Working knowledge of cGMP requirements and pharmaceutical development standards • Strong strategic, analytical, and problem-solving skills, with the ability to anticipate risks, develop contingency plans, and drive timely, high-quality results • Excellent communication, interpersonal, and project leadership skills, with the ability to influence stakeholders, manage cross-functional and external relationships, and communicate complex concepts to diverse audiences • Highly organized, detail-oriented, and self-directed, with the ability to manage multiple priorities in a fast-paced, dynamic environment • Willingness to travel domestically and internationally (5-10%)
• 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 • Employee assistance program • Fitness benefits • Employee clubs and activities
Apply Now🔥 18 hours ago
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