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.
Are you ready to play a key role in ensuring the quality and compliance of cutting‐edge pharmaceutical manufacturing operations?
We are looking for a QA Associate to join our Quality team at the Eli Lilly Italia Manufacturing Site in Sesto Fiorentino.
As a QA Associate, you will serve as the primary Quality contact within both the Project Team and the Formulation Cartridges Process Team. You will support the implementation of a new formulation suite from its earliest stages,

acting as a trusted partner to cross‐functional teams and a key point of escalation for quality matters.
What You'll Do
Lead quality oversight for the formulation project, including qualification phases and start‐up of the new suite
Ensure consistent application of cGMP standards and Eli Lilly quality requirements across the area
Serve as the accountable escalation point for quality issues arising in the project or production area
Support preparation for Regulatory inspections and contribute to the site self‐inspection program
Investigate deviations in the Cartridge area and perform Quality Assessments in Veeva QMS
Review and approve qualification protocols and procedures
Act as Media Fill observer and approve work orders where applicable
Actively contribute to site Quality Systems and Quality Culture initiatives
What We're Looking For
Master's Degree in a Scientific discipline
Experience in pharmaceutical industry operations
Solid knowledge of current GMP

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