Principal Associate - HSE

Role: Lead HSE professional supporting the startup of Lilly's new GMP manufacturing site for monoclonal antibodies and bioconjugates in Virginia. Responsibilities: develop and improve the site HSE Management System; lead safety/health program development; act as technical expert on compliance and legislation; foster safety culture; deliver training and initiatives; manage safety performance metrics; lead audits and assessments; collaborate with internal and external partners; mentor HSE team members. Requirements: Bachelor's in occupational health, safety, engineering, or related field; 5+ years’ experience in regulated GMP environments; proven ability to interpret safety regulations and develop programs; authorized to work in the U.S. without sponsorship. Preferred: experience supporting greenfield or startup projects in pharma or regulated manufacturing; strong organizational, analytical, communication, and leadership skills. HighValue: GMP manufacturing, biologics (monoclonal antibodies, bioconjugates), startup phase, safety program development, regulatory compliance, cross-functional collaboration, site culture building. WorkSetup: Full-time, based in Goochland County, VA; role involves significant project/support collaboration during construction and startup phases.