This job is closed
We regret to inform you that the job you were interested in has been closed. Although this specific position is no longer available, we encourage you to continue exploring other opportunities on our job board.
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. The Operator position resides in the Product delivery (PD) organization and supports the B358 clinical trial parenteral manufacturing plant. This position will report to the CT Leader Parenteral Operations. The Operator will draw upon previous parenteral manufacturing experience to support the B358 CT manufacturing business needs for this GFD capital project. Initial responsibilities will focus on design reviews, procedure and training development, commissioning and qualification support and then startup of the facility. Ultimately, the position will work in B358 CT parenteral manufacturing operations. The Operator will be responsible for manufacturing/inspecting drug product while ensuring compliance with all policies/procedures. The Operator may be required to work in Formulation, Filling, Component Preparation, and/or Inspection.