Quality Assurance Associate

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At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life‐changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, self‐less work—but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Interessato/a a questo ruolo? Può trovare tutte le informazioni pertinenti nella descrizione qui sotto.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 the Filling Cartridges Process Team, acting as a trusted partner to cross‐functional teams and a key point of escalation for quality matters.
What You'll Do
- 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 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
- 1-2 years of experience in pharmaceutical industry operations
- Basic knowledge of current GMPs, pharma

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