Chemist - Quality Control

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 put people first and are looking for people who are determined to make life better for people around the world.

The Chemist – QC in Indianapolis Radioligand Therapy (IRLT) group performs accurate and timely testing of routine and some non-routine radioactive lab samples in accordance with GMP and safety guidelines. The chemist completes second-person verification of others’ results and participates in laboratory analytical investigations, equipment evaluations and qualifications, and some quality system improvement initiatives by executing well-defined protocols and procedures. The chemist shares technical information and best practices within plant sites or groups.

• Sample Analysis and Reporting
  • Verify (SPV) analytical data of other analysts within the lab as requested.
  • Accurately and safely perform analytical test methods or related support activities per procedures or protocols. Use technical knowledge to review and interpret data for conformance to procedures, standards, protocols, and real-time recognition of aberrant data and results.
  • Perform data entry and review 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.
  • Problem Solving:
    Recognize deviations from test methods or procedures and initiate analytical investigations, including root cause investigations.
  • Participate in investigations for deviations, including lead investigator duties as appropriate.
  • Assist in troubleshooting equipment and methods as required.

• Assist in improving quality systems by creating or revising worksheets and other lab documentation systems.
• Identify and communicate opportunities for improvement in daily work activities.
• Review SOPs for executable as written.
• Share technical information and best practice within plant sites or groups.

• 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.

• Bachelor’s degree in a science field related to the lab (e.g., chemistry, biochemistry, biology, etc.).
• Preferred 1+ years of experience in a GMP analytical lab.

• Experience with radioactive materials a plus.
• Proficiency with computer systems LIMS, Empower, Chromeleon, Excel, etc.
• Proficiency with UHPLC, pH meters, ICPMS, Rad detectors, Dose calibrators, and Gamma detectors, among others, a plus.
• 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.

• Position supports a 4 day, 10 hour shift (Saturday-Wednesday) or (Wednesday-Sunday) with both day and night shifts available. Night shift preferences will be considered favorably.
• Tasks may require repetitive motion and standing for long periods of time.
• Must be able to lift at least 5 liters of liquid.
• Overtime work required, as necessary.
• Note:
  
  When applying internally for a position your current supervisor receives notification that you have applied to the position. We encourage employees to discuss the opportunity with their supervisor prior to applying.

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