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Lilly Process Engineer-Vision in Indianapolis, Indiana

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 39,000 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.

Responsibilities :

The Process Engineering Center (PEC) is a group of skilled engineering practitioners who possess deep technical expertise and have access to appropriate lab facilities. The PEC partners with plant engineers, site process engineers, Global Facility Delivery engineers, development engineers, and scientists to provide rigorous technical solutions.

  • Provide ongoing technical support to sites, domestic and global for Automated Inspection (ASIM/AVIM/CAS). Interface with site technical experts in Engineering.

  • Technical leadership – Serves as technical resource in Aseptic Processing and Parenteral Technologies, specifically, Filling as well as consulting support on technical issues.  Parenteral sites supported include Indy Parenteral, Fegersheim, Sesto, RTP, and Suzhou. 

  • Major Capital Support - Provide technical leadership, both conceptual and detailed design, to Global Facilities Delivery on major capital projects; support the Design Delivery Gate Review process by maintaining Gate protocols and executing gates on major projects and participates in Manufacturability Review assessments.

  • Assist sites globally with technical evaluation, master planning, technology assessments, and specific problem resolution including troubleshooting and root cause analysis

  • Knowledge sharing - Provide ongoing technical support to site plant engineering groups, domestic and global; provide technical mentoring to Lilly engineers.

  • Assist with the investigation, development, and integrate emerging technology and capabilities applicable to the Development and Parenteral manufacturing process to meet production and compliance requirements.

  • Reviews and prepares protocols and technical reports.

Basic Qualifications :

  • Bachelors degree in Engineering or related technical field.

  • 3 plus years in cGMP manufacturing or manufacturing support experience in Aseptic Manufacturing

  • Project management experience

Additional Skills/Preferences :

  • Ability to work effectively with outside suppliers.

  • Ability to work across boundaries (functional, geographic, external company, etc).

  • Thorough technical understanding of the quality systems and regulatory requirements,

  • Experience in root cause analysis, and

  • Experience in solving technical problems and implement solutions.

Additional Information :

  • Must be able to travel up to 25% of the time, US and international.

  • Will require occasional work in a variety of manufacturing environments; some safety equipment and/or gowning may be required.

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.

Lilly is an EEO/Affirmative Action Employer and 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.

At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people.​ We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!