
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.
🔥 4 minutes ago
🇺🇸 United States – Remote
đź’µ $153k - $290.4k / year
⏰ Full Time
đźź Senior
đź‘” Director
đź‘» Ghost score 0%
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• Lead work with external vendors and oversee nonclinical formulation development across programs • Directly manage CROs and CDMOs • Execute physicochemical characterization and pre-formulation studies for New Chemical Entities • 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 formulation, DS and DP stability, and supply guidance at cross-functional meetings • Coordinate shipments supporting nonclinical and clinical development supply requirements • Assist with formulation 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 • Report to the Executive Director, CMC
• Advanced degree in Chemistry, Pharmaceutical Sciences, or a related discipline; Ph.D. strongly preferred • 10+ years of drug product/formulation development experience supporting nonclinical and clinical programs • Expertise across oral, subcutaneous, and intravenous dosage forms for small molecules • Deep technical expertise in developing and manufacturing poorly soluble BCS Class II/IV compounds • Strong understanding of pharmaceutical sciences and engineering principles for liquid and solid dosage form development through clinical and commercial manufacturing • Working knowledge of analytical and solid-state characterization techniques, including HPLC/UPLC, XRPD, DSC, TGA, DVS, and related methodologies • Experience managing external development and manufacturing partners, including CROs, CDMOs, and CMOs • Solid understanding of cGMP requirements • Ability to lead multiple complex programs in a fast-paced environment, with project management, prioritization, resource management, and organizational skills • Excellent communication, presentation, and interpersonal skills • Ability to influence stakeholders, build internal and external partnerships, and communicate complex scientific concepts to diverse audiences • Strategic, hands-on leadership with decision-making, problem-solving, resilience, and a track record of delivering high-quality results with urgency and integrity • Willing and able to travel domestically and internationally as needed
• 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, including 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
Apply Now🔥 5 minutes ago
Field Medical Affairs leader advancing Regeneron respiratory medicines across Southern California and the Central Valley. Building scientific partnerships with healthcare providers, payers, and investigators.
🇺🇸 United States – Remote
đź’µ $176.1k - $287.3k / year
đź’° Post-IPO Equity on 2023-10
⏰ Full Time
đźź Senior
đź‘” Director
🦅 H1B Visa Sponsor
🔥 40 minutes ago
Field Medical Affairs leader supporting Pierre Fabre’s oncology portfolio and healthcare stakeholders across the Midwest. Building KOL relationships, guiding medical strategy, and supporting clinical studies.
🔥 44 minutes ago
Senior Director leading provider contracting, network development, and optimization for Centene’s healthcare plans. Developing market strategies, negotiating provider agreements, and supporting new business launches in Texas.
đź•’ 3 days ago
Senior Director overseeing institutional loan servicing, repayment, and collections for Arizona College of Nursing. Improving borrower outcomes through portfolio analytics, compliance, vendors, and team leadership.
đź•’ 3 days ago
Associate Director configuring Adobe Workfront, Fusion automation, and integrations for Bounteous’s enterprise AI services clients. Driving implementation, training, support, and workflow optimization.
🇺🇸 United States – Remote
đź’µ $105k - $130k / year
đź’° Private Equity Round on 2021-08
⏰ Full Time
đźź Senior
đź‘” Director
🦅 H1B Visa Sponsor