Sr. Director - Quality Control Laboratories

Role: Senior Director of QC Laboratories overseeing analytical operations at Lilly's new API manufacturing site in Huntsville, Alabama, supporting GMP compliance and advanced analytical capabilities for biopharma modalities. Responsibilities: build and lead a high-performing, GMP-compliant QC organization; develop laboratory strategies aligned with digital, paperless visions; coordinate with global quality and operations teams; manage regulatory inspections and ensure safety standards; foster personnel development and technical capability within the team. Requirements: Bachelor's degree in chemistry, microbiology, engineering, or related; 10+ years supporting complex analytical testing (chromatography, bioassays, characterization); 2+ years in GMP/cGMP environment; 5+ years leadership experience; expertise in analytical quality systems and regulatory submissions. Preferred: proficiency with computer systems, technical writing, strong communication, cross-functional influence skills; ability to travel (~10%). High-value biopharma specifics: supporting production of APIs for multiple modalities, including new modalities, in a GMP environment, with a focus on automation and analytical excellence. Cross-functional collaboration with global quality, manufacturing, and site leadership. Work setup: full-time, based in Huntsville with some travel.