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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.…
Lead the creation of regulatory and clinical documents for gene-editing cardiovascular therapies, collaborating with cross-functional teams to ensure scientific accuracy and compliance with FDA/EMA guidelines.
Leads GenAI software products at a global pharma company, defining vision, strategy, and execution while collaborating with engineering and design teams to deliver patient-focused solutions using modern tech stacks.
Lead a team of QC microbiology leaders to build and operate a new GMP manufacturing site, ensuring compliance, inspection readiness, and supply of life-saving medicines.
Lead cross-functional teams to start up a new gene-therapy manufacturing plant, ensuring quality, supply, and regulatory compliance while managing relationships with contract manufacturers.
Lead small-molecule API manufacturing operations at a new Lilly facility in Houston, overseeing daily production, safety, quality, and startup activities while building the site’s culture and systems.
Lead a technical team to oversee biopharmaceutical manufacturing processes for monoclonal antibodies and bioconjugates, ensuring GMP compliance and operational excellence during facility startup.
Maintains and supports lab informatics systems (NuGenesis SDMS/ELN and Empower CDS) for a global pharmaceutical company, ensuring GMP compliance, data integrity, and smooth lab operations.
Lead supply chain, warehousing, and logistics for a new GMP API manufacturing site, planning production, managing inventory, and ensuring regulatory compliance while building the startup team and systems.
Leads global communications and consumer campaigns for Lilly’s cardiometabolic medicines (e.g., Mounjaro, Zepbound) across 40+ markets, managing media relations, issues management, and medical meeting communications.
Lead the Occupational Health team at a pharmaceutical manufacturing site, overseeing clinical services, governance, and change initiatives to ensure employee wellbeing and regulatory compliance.
Principal Process Engineer designs and optimizes purification systems for biologics, peptides, and oligonucleotides at Lilly’s new Medicine Foundry, ensuring GMP compliance and scaling processes for clinical trial APIs.
Oversee large-scale manufacturing capital projects for a global pharmaceutical company, coordinating teams and contractors to deliver safe, compliant facilities from design through operation.
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