Eli Lilly and Company is a global healthcare leader headquartered in Indianapolis, Indiana. The Quality Engineer is responsible for providing technical guidance and leadership regarding quality standards at the LP1 site, focusing on utilities, bulk distributed materials, and facilities/equipment qualification.
Provide direct quality oversight to LP1 manufacturing and laboratory operations and assist others in interpretation of regulatory and corporate requirements
Provide quality guidance, technical support and recommendations to equipment and process issues and continuous improvement initiatives
Work with cross functional teams to implement QA objectives
Prepare for and participate in internal and external regulatory inspections
Maintain and improve facility, utility, maintenance and equipment (FUME) quality systems
Qualification
Required
Bachelors Degree in Engineering or science related field
1+ years in pharmaceutical industry
Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1
Preferred
Previous experience in pharmaceutical industry
Previous experience in QA, TS/MS QC or Engineering
Prior work with cGMPs or external regulations
Previous experience with root cause investigations
Effective problem-solving and analytical skills to resolve operational issues
Benefits
Company bonus
Company-sponsored 401(k)
Pension
Vacation benefits
Eligibility for medical, dental, vision and prescription drug benefits
Flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
Life insurance and death benefits
Certain time off and leave of absence benefits
Well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
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