Associate - Manufacturing Process

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.

Job Description

Eli Lilly Italia is looking for a Manufacturing Process Associate to join our Manufacturing Operations team at the Sesto Fiorentino (FI) site, within the Cartridge Formulation production line dedicated to injectable pharmaceuticals.

In this role, the Manufacturing Process Associate reports directly to the Line Manager and plays a central role in coordinating and supporting daily manufacturing operations. The position ensures that all production phases are executed efficiently, safely, and in compliance with regulatory standards.

The focus of this role is primarily operational, ensuring the smooth execution of daily production activities, proper adherence to procedures, and timely completion of the manufacturing plan. Alongside this, the role contributes to continuous improvement initiatives aimed at optimizing efficiency and maintaining technical excellence.

As a member of the Process Team, the Manufacturing Process Associate works closely with Shift Supervisors, production crews, and technical support functions, promoting open communication and alignment across all shifts. The position contributes to sustaining a proactive, safety-focused, and quality-oriented work environment.

Key Responsibilities:

Actively participate in the daily organization and coordination of shop floor activities within the Cartridge Formulation Line

Ensure the efficient and compliant execution of production operations, working closely with Production Supervisors and the Process and Technical Teams

Collaborate with Planning to define and adjust the production plan, ensuring alignment with operational priorities

Support Production Supervisors in achieving daily production targets, promptly responding to operational issues or deviations while maintaining Safety and Quality standards

Collect, analyze, and report production metrics and performance data

Conduct deviation investigations and prepare related reports

Manage small Capital and Operating Expenses projects related to the production area

Contribute to maintaining technical knowledge and training standards within the department

Actively promote and enforce an interdependent HSE culture

Partner with QA Associates to sustain and strengthen the Quality culture, ensuring all operations are performed and documented according to GMP procedures

Basic Requirements:

Master’s degree in a scientific discipline (Engineering, Biology, Chemistry, Biotechnology)

2–5 years of experience in complex manufacturing environments (pharmaceutical experience preferred)

Good command of English

Sound knowledge of Good Manufacturing Practices (GMP) and HSE regulations

Solid understanding of manufacturing processes and operations

Additional Skills/Preferences:

Strong organizational and planning skills

Leadership and communication abilities

Results-driven and proactive mindset

Problem-solving and negotiation skills

What We Offer:

Step into a role where your hands-on operational expertise and commitment to excellence are recognized and valued. As part of our team, you will benefit from:

Competitive Salary: Base salary with annual performance-based variable component

Relocation Package: Available based on candidate location

Comprehensive Benefits: Extensive welfare and insurance coverage

Annual Salary Review: Recognition and reward for continued contribution, with opportunities for growth and eligibility for stock option packages aligned with company performance

golatori (AIFA, FDA, etc.).

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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