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Associate - qa formulation line 3 (re)

Re
Eli Lilly and
Pubblicato il 8 gennaio
Descrizione

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 aQA Associateto join our Quality team at theEli Lilly Italia Manufacturing Sitein 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 GMPs, pharmaceutical legislation, and regulatory requirements
Good command of English (minimum B2 CEFR level)
Strong communication and influencing skills
Collaborative mindset with a pragmatic, compliance-oriented approach
This position is based on-site, with up to 4 days of remote work per month.
What We Offer
Joining Eli Lilly Italia means stepping into a role where your expertise is recognized and rewarded from day one.
Competitive compensation— a strong base salary plus an annual variable component tied to your objectives
Relocation support— a relocation package available depending on your location
Comprehensive benefits— an extensive welfare and insurance plan
Annual salary review— with advancement opportunities based on your performance
Long-term upside— eligibility for a stock option package, linking your growth to the company's success
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 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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