Process Engineer - Global Parenteral Program

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 is looking for a Process Engineer to support the Global Parenteral Program Team (GPP), a cross-functional group dedicated to supporting and harmonizing the aseptic filling lines of the parenteral syringe platform, which is expanding rapidly.

The figure, inserted in an international context, will be responsible for supporting the multiple lines of the PFS (Pre-Filled Syringes) global platform from a technical and strategic point of view. The latter currently consists of several production lines, distributed over different production sites (in Italy and the US).

Working with the GPP Team, local site groups, and equipment suppliers, the Process Engineer will be responsible for ensuring the completion of the design and validation phases of the equipment, as well as providing the appropriate support in the production start-up phase.

The role will require frequent and prolonged travel to Lilly sites located in the US.

Main responsibilities of the role:

• In-depth knowledge of parenteral processes and equipment (it will be a valued experience in pre-filled syringes production).

• Design of machine parts and software logic of the equipment (in collaboration with other team members and with the supplier's SME) with a view to bug fixes and continuous improvement.

• Support for troubleshooting activities and adequate technical coaching.

• Execution of tests, validation, and technical process studies.

• Production and review of technical and validation documentation, in accordance with cGMP.

• Knowledge sharing and on-the-floor training for members of the sites hosting the new production lines.

• Support for the execution of qualification/validation activities (FAT, SAT, PQ, CD, AFPT ...) at suppliers and sites.

• Management and prioritization of continuous improvement activities with a view to aligning and harmonizing the lines pertaining to the network.

Minimum requirements:

• BS in Mechanical, Chemical, or Electronic Engineering.

• Previous experience of at least 2+ years in pharmaceutical production, preferably pre-filled syringes filling lines.

Additional Preferences / Information:

• Filling equipment is the preferred experience, specifically isolators and PFS filling lines.

• High flexibility and teamwork attitude.

• Willingness to travel at least 30% of the time.

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Actual compensation will depend on a candidat