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.
Eli Lilly Italia is looking for a QA Associate to join our Manufacturing Operations team at the Sesto Fiorentino (FI) site, within the Pre-Filled Syringes (PFS) area.
In this role, the QA Associate reports directly to the Quality Manager and acts as the Quality point of contact for the PFS area. The role ensures the application of cGMP and Eli Lilly Quality standards, supporting compliance and driving a strong Quality culture. Depending on seniority, the scope of responsibilities and complexity of activities may evolve.
Key ResponsibilitiesManage the escalation process in case of Quality issues within the production area
Support inspection readiness for Regulatory Agencies and contribute to the site self-inspection program
Collaborate in investigations related to the PFS area, performing Quality Assessment of observations and deviations in Trackwise
Approve Change Controls (CHG) as part of Quality oversight
Perform Batch Review and Batch Disposition of semi-finished products
Review procedures (QP/LV) and serve as instructor for selected trainings and procedures
Execute Quality process monitoring and provide inputs for documentation such as APR and AQMS
Act as Media Fill observer
Approve work orders, where applicable
Contribute to site Quality Systems and Quality Culture initiatives
Master’s degree in a scientific discipline
Experience in pharmaceutical industry operations will be a strong plus
Good knowledge of English
Strong grasp of Quality principles and their application in pharmaceutical manufacturing
Ability to prioritize and assess criticality of Quality issues, with strong problem-solving and decision-making skills
Effective communicator with solid interpersonal, influencing, and teamwork abilities
Organized, pragmatic, and compliance-oriented mindset
What We Offer
Step into a role where your expertise is recognized, appreciated, and rewarded. As a member of our team, you can expect:
Competitive Salary: We offer a competitive base salary supplemented by an annual variable component based on achieving objectives.
Relocation Package: You will be eligible for a relocation package based on your location.
Comprehensive Benefits: Enjoy a well-rounded welfare package, including an extensive insurance plan.
Lilly 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 (https://careers.lilly.com/us/en/workplace-accommodation) 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.
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.
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What We Do
Eli Lilly and Company engages in the discovery, development, manufacture, and sale of products in pharmaceutical products business segment.
For more than a century, we have stayed true to a core set of values – excellence, integrity, and respect for people – that guide us in all we do: discovering medicines that meet real needs, improving the understanding and management of disease, and giving back to communities through philanthropy and volunteerism.
