Eli Lilly and Company→
Manufacturing Science - Intern to Intern at Eli Lilly and… · US:…
InternshipOn-siteFull-timeUS: Research Triangle Park NC$43k–$110k/yr
Skills
laboratory practicesmanufacturing practicesanalytical techniqueswet chemistryhplcicpatomic absorption (aa)titrationmicrobiological assaysprocess improvementdata analysisquality controlquality assurancepharmaceutical manufacturingregulatory compliance
Job Description
Summary: Eli Lilly and Company is a global healthcare leader headquartered in Indianapolis, Indiana. They are seeking a Manufacturing Science Intern to contribute to the Tech Services Manufacturing Sciences or Quality organizations, focusing on ensuring reliability of manufacturing systems and implementing continuous improvements.
Responsibilities:
- Ensuring reliability of our manufacturing and utility systems
- Searching for and implementing continuous improvements
- Maintaining our facilities and processes in a state of compliance with US and global regulations
- Managing capital projects
- Designing and developing drug delivery systems
- Provide a practical real-life solution to a manufacturing business-related technical project
- Understand the scientific principles required for manufacturing pharmaceutical substances, including the interaction with equipment
- Provide technical support to non-routine (e.g. deviation) investigations
- Be capable of preparing relevant technical documents, such as Reports, Change Controls, Regulatory submissions, Deviations, Protocols, etc
- Utilize the principles of Good Laboratory Practices/Good Manufacturing Practices and principles to analyze process intermediates, active pharma ingredients, and drug product in a Quality Control Lab (QCL) using analytical techniques such as wet chemistry, HPLC, ICP, AA, Titration, and/or Microbiological Assays
- Actively run a technical improvement agenda within the area of responsibility to drive process improvement
- Monitor and appropriately react to established statistically based metrics in real time to assess process variability and capability
- Work within cross-functional teams in a positive fashion to implement TSMS or Quality objectives and deliver business plans and quality objectives
- Work individually and with a supervisor to determine and achieve project goals driving process productivity through the implementation and execution of the project
- Document and present project accomplishments and progress
Required Qualifications:
- Currently attending college and completion of a BS or MS scientific discipline degree by August 2028
- Successful completion of a previous Lilly internship
- Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor the following work authorization or visas for this role: F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1
- Analysis/problem assessment skills, communication (oral and written) skills, information/data monitoring skills, quality orientation, and teamwork/interpersonal skills
Preferred Qualifications:
- Previous internship experience within the pharmaceutical industry
Required Skills: Laboratory Practices, Manufacturing Practices, Analytical techniques, Wet chemistry, HPLC, ICP, Atomic Absorption (AA), Titration, Microbiological Assays, Process improvement, Data analysis, Quality Control, Quality Assurance, Pharmaceutical manufacturing, Regulatory compliance
Benefits: 1 week of paid time off during the Lilly summer shutdown, Competitive salary, Free parking at their work site, Access to Lilly’s onsite facilities, Subsidized housing
Benefits
1 week of paid time off during the Lilly summer shutdown
Competitive salary
Free parking at their work site
Access to Lilly’s onsite facilities
Subsidized housing