Technician-QC-IAPI-Bulk Testing Lab

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.

The Technician – QC in Indianapolis Active Pharmaceutical Ingredient (IAPI) group performs accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. The technician completes second person verification of other's results. The technician also participates in laboratory analytical investigations, equipment evaluations and qualification, and some quality system improvement initiatives by executing well-defined protocols and procedures.

The technician shares technical information and best practice within plant sites or group.

• Verify (SPV) analytical data of other analysts within the lab as requested.
• Accurately and safely perform analytical test methods or related support activities as per procedures or protocols. Uses technical knowledge in the review and interpretation of data for conformances to procedures, standards, protocols, and/or real-time recognition of aberrant data and results.
• Perform data entry and reviews own work for accuracy in accordance with laboratory procedures, standards and GMP requirements.
• May perform holistic review of data for release of data from the laboratory.

• Recognizes when a deviation from test methods, procedures, et cetera has occurred and initiates analytical investigations and participates in a Root Cause Investigations.
• Participates in investigations for deviations.
• Assists in troubleshooting equipment and methods as required.

• Assist in improvement of quality systems by creating or revising worksheets and other lab documentation systems.
• Identifies and communicates opportunities for improvement initiatives in daily work activities.
• Reviews SOPs for executable as written.
• Shares technical information and best practice within plant sites or group.

• Assist with drafting protocols for non-routine testing or validation with appropriate guidance.
• Assist in developing equipment qualification protocols with appropriate guidance.
• Perform routine equipment calibrations or maintenance.
• Comply with and assist with implementing safety standards.
• Execute notification to management when required by procedures or standards.
• Initiate lab deviations
• Train and mentor others. Assist with developing training materials.

• Associate’s degree in a science field related to the lab (e.g., chemistry for Chem. Labs) or 1+ years of demonstrated relevant experience in a GMP analytical lab

• Proficiency with computer systems LIMS, Empower, Excel, etc.
• Ability to work in a lab environment, including wearing appropriate PPE and other safety required equipment and considerations.
• Demonstrate strong math and documentation skills.
• Demonstrate strong oral and written communication and interpersonal interaction skills.

• Sunday-Thursday 8 Hour Evening to Night Shift.
• Tasks may require repetitive motion and standing for long periods of time.
• Must be able to lift at least 5 liters of liquid.
• Overtime or weekend work required, as necessary.

If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form at  for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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