Manufacturing Science Intern

Eli Lilly and Company • Us, IN

3d • Onsite

About The Position

The Manufacturing Science Intern is a temporary summer position lasting 12 continuous weeks beginning in May or June 2027. Interns are assigned a project within Tech Services Manufacturing Sciences (TSMS) or Quality, contributing to work in science and technology, direct process support, or analytical laboratory support. The role provides exposure to the technology, science, and regulatory requirements involved in manufacturing commercial medicines in therapeutic areas including diabetes, oncology, and endocrinology. Project areas may include parenteral products, bulk processing of small and large molecules, and global delivery devices.

Interns work with engineering, manufacturing, and science professionals, including senior management. They receive opportunities for professional development and social events, and present project findings and accomplishments to science and manufacturing professionals at the end of the internship. The role also offers opportunities to build fluency with business AI tools, with an emphasis on critical thinking, accuracy, confidentiality, and ethical use.

Requirements

• Currently attending college and expected to complete a BS or MS in a scientific discipline by August 2029.
• Authorized to work in the United States on a full-time basis; the employer will not sponsor or support the listed visa or work authorization categories.
• Analysis and problem-assessment skills.
• Oral and written communication skills.
• Information and data monitoring skills.
• Quality orientation.
• Teamwork and interpersonal skills.

Nice To Haves

• Previous internship experience in the pharmaceutical industry.
• Prior experience using AI tools, such as generative AI platforms, automation tools, or AI-assisted research or analytics tools, in an academic, project, or work setting.

Responsibilities

• Deliver a practical solution to a manufacturing business-related technical project.
• Understand the scientific principles of pharmaceutical-substance manufacturing, including interactions with equipment.
• Provide technical support for non-routine investigations, such as deviation investigations.
• Prepare technical documents such as reports, change controls, regulatory submissions, deviations, and protocols.
• Apply Good Laboratory Practices and Good Manufacturing Practices when analyzing process intermediates, active pharmaceutical ingredients, and drug products in a Quality Control Lab using applicable analytical techniques.
• Run technical improvement initiatives within the assigned area to drive process improvement.
• Monitor statistically based metrics in real time and respond appropriately to assess process variability and capability.
• Collaborate positively with cross-functional teams to implement TSMS or Quality objectives and deliver business and quality plans.
• Work independently and with a supervisor to set and achieve project goals that improve process productivity.
• Document and present project accomplishments and progress.
• Use AI tools with curiosity and critical thinking while prioritizing accuracy, confidentiality, and ethical standards.

Benefits

• One week of paid time off during the Lilly summer shutdown (July 5–9).
• Competitive salary.
• Free parking at the work site and access to onsite facilities.
• Subsidized housing if the internship requires relocation from another location.
• Intern activities, including sporting events, dinners, lunch-and-learns, and volunteer activities, as well as professional development and learning opportunities.
• Interns may be considered for full-time positions based on internship performance.

What This Job Offers

• Career Level: Intern