PpAt 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.
/p pAre you ready to play a key role in ensuring the quality and compliance of cutting-edge pharmaceutical manufacturing operations?
/p pWe are looking for a bQA Associate /b to join our Quality team at the bEli Lilly Italia Manufacturing Site /b in Sesto Fiorentino.
/p pAs 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.
/p h3What You'll Do /h3 ul liLead quality oversight for the formulation project, including qualification phases and start-up of the new suite /li liEnsure consistent application of cGMP standards and Eli Lilly quality requirements across the area /li liServe as the accountable escalation point for quality issues arising in the project or production area /li liSupport preparation for Regulatory inspections and contribute to the site self-inspection program /li liInvestigate deviations in the Cartridge area and perform Quality Assessments in Veeva QMS /li liReview and approve qualification protocols and procedures /li liAct as Media Fill observer and approve work orders where applicable /li liActively contribute to site Quality Systems and Quality Culture initiatives /li /ul h3What We're Looking For /h3 ul liMaster's Degree in a Scientific discipline /li liExperience in pharmaceutical industry operations /li liSolid knowledge of current GMPs, pharmaceutical legislation, and regulatory requirements /li liGood command of English (minimum B2 CEFR level) /li liStrong communication and influencing skills /li liCollaborative mindset with a pragmatic, compliance-oriented approach /li /ul pThis position is based on-site, with up to 4 days of remote work per month.
/p h3What We Offer /h3 pJoining Eli Lilly Italia means stepping into a role where your expertise is recognized and rewarded from day one.
/p ul liCompetitive compensation — a strong base salary plus an annual variable component tied to your objectives /li liRelocation support — a relocation package available depending on your location /li liComprehensive benefits — an extensive welfare and insurance plan /li liAnnual salary review — with advancement opportunities based on your performance /li liLong-term upside — eligibility for a stock option package, linking your growth to the company's success /li /ul pLilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions.
If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( for further assistance.
Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
/p pLilly 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.
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