Inspection Operator, IPM - Nights - Fulltime
Listed on 2026-03-01
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Manufacturing / Production
Manufacturing Engineer, Manufacturing Production, Production Associate / Production Line, Quality Engineering
Location: Indianapolis
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.
For 140 years, Lilly has manufactured medicines that improve people’s lives around the world. We produce our medicines using some of the most sophisticated manufacturing technologies and rigorous quality standards. Lilly Manufacturing strives for excellence in its process, standards, procedures and behaviors to develop medicines with safety first and quality always.
Path / LevelB1
The annual base salary for this position in country = United States of America ranges from: $35,000.00 - $80,000.00 USD
The job profiles on this job requisition are:
Manufacturing-Process-B1-Prod Oper, Manufacturing-Process-B2-Prod Oper, Manufacturing-Process-B3-Prod Oper
Note:
Roles are posted at the lowest level of a band, however, employees should search across all levels of the band to identify all opportunities. Employees hired on banded positions (ex: P1-P3, R1-R2, B1-B3, etc.) transfer at their current level, despite the level indicated on the job posting. For example, if a P2 candidate is selected for a P1-P3 banded position, the candidate will remain a P2 in the new role.
To understand a U.S. role’s salary range, employees should visit the U.S. Lilly Now Total Base Pay page () or contact HR Solutions. For roles located in Puerto Rico and outside the United States, employees should contact local HR or HR Solutions ().
Quick Benefit Overview- Medical, Dental, Vision, Prescription benefits are effective on your first day of employment
- Paid vacation- starting annually at 120 hours (prorated based on start date)
- $3,000 sign‑on bonus
- The Operator will work in the Indianapolis Parenteral Manufacturing site where Parenteral products for domestic and international markets are formulated, filled, and inspected. The primary purpose of the job is to safely inspect high quality pharmaceutical filled syringes utilizing Lilly standards by following good manufacturing practices in controlled facilities.
- Responsible for maintaining a safe work environment, working safely, adhering to parenteral plant safety policies and procedures, and accountable for supporting all HSE Corporate and Site Goals.
- Setup and operations in non‑aseptic manufacturing processes, including the set‑up, use, and/or operation of automated and semi‑automated inspection machines in controlled facilities.
- Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product.
- Document process steps on appropriate batch documentation (paper and electronic).
- Unloading / loading of materials for use in manufacturing areas, storage of material in appropriate storage zones and ASRS (Automated Storage Retrieval System).
- High School diploma / GED
- Basic math skills
- Basic computer skills, including the use of HMIs and other computer terminals used to monitor equipment status, document production activities, and the capability to learn in more detail
- Completion of Post Offer Exam, or Completion of Work Simulation if applicable.
- Must pass a “fitness for Duty” physical exam
- Must pass eye exam and not be color blind.
- 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.
- Ability to demonstrate attention to detail
- Excellent documentation skills
- Experience with GMPs
- Experience working in a manufacturing environment, preferably pharmaceutical manufacturing experience
- Certified to operate all types of powered industrial…
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