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 35,000 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. Eli Lilly Italia is looking for a TSMS Process Support Associate Director to join the Manufacturing Team in Sesto Fiorentino (FI). He/She will be responsible of a team of SME of the secondary loop in the TSMS function, supporting both Parenteral and Device Assembly & Packaging Operations. In additon, He/She will be responsible that the team investigates major issues on the lines as well as lead continuous improvement activities and major project. The Associate Director will also be part of the TSMS Staff and will collaborate with the Site Technical Teams and Flow Teams. Main responsibilities of the role: - Guarantee the support, through dedicated resources in the TS/MS area, for the activities of the Technical Teams, both Parenteral and Device Assembling & Packaging - Contribute to the definition of plant project priorities, in agreement with the Flow Teams and the Technical Team coordinators - Ensure the alignment, within his/her area of responsibility, of the processes implemented at Sesto vs global reference standards (internal and external) - Might act as Project Manager for complex or cross-functional initiatives - Supervise highly experienced personnel belonging to the Technical Teams - Prepare, personally or through collaborators, technical evaluation documents in support of complex operational events or practices - Manage troubleshooting, personally or through collaborators, for serious quality problems in production or in case of major deviations, coordinating task forces created for specific cases - Interact with Network Technical forum (e.g. GPP, IDM, Global Packaging) and influence qualification strategies - By means of qualified personnel, ensure adequate support for the implementation of improvement projects and the resolution of equipment problems while coaching the new emerging technical talent at the site - Support GMP inspections as a SME Minimum requirements: - Scientific Master’s Degree - 5 years of experience in Pharmaceutical Company (parenteral knowledge preferred) - Fluent English Additional skills/preferences: - Troubleshooting - Project Management - Good communication and influencing skills - Teamworking attitude - Knowledge of regulatory/compliance expectation Additional Information: - Position located in Sesto Fiorentino - Full time position - 5/10% travel - The contractual framework for this role corresponds to _quadro _of the national contract for the pharmaceutical sector.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.