Associate - Cartrdiges Formulation Operations

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