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.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

$63,000 - $140,800

Description:

The Chemist in the Raw Materials Laboratory performs accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. This individual completes second person verification of others results and also assists in laboratory root cause investigations, equipment evaluations and qualifications, and some quality system improvement initiatives by performing well-defined protocols and procedures. The Chemist shares technical information and best practice within plant sites or group.

Responsibilities:

• 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 conformance to procedures, standards and protocols and/or real-time recognition of aberrant data and results.

• Perform data entry and review work ensuring accuracy in accordance with laboratory procedures, standards and GMP requirements.

• May perform comprehensive review of data for release of data from the laboratory.

• Recognizes when a deviation from procedures, etc. has occurred and initiates and participates in a Root Cause Investigation.

• Performs investigations for deviations.

• Troubleshoot equipment and methods as required.

• Assist in improvement of quality systems by crafting or revising worksheets and other lab documentation systems.

• Evaluates and communicates opportunities for improvement initiatives in daily work activities.

• Contribute to development of PQEs.

• Reviews SOPs for executable as written.

• Shares technical information and best practice within plant sites or group.

• Write protocols for non-routine testing or validation with appropriate guidance.

• Develops equipment qualification protocols with appropriate guidance.

• Perform routine equipment calibrations or maintenance through execution of well- defined protocols.

• Follow and implement safety standards.

• Handles notification to management when required by procedures or standards.

• Initiate change controls and deviations.

• Train and mentoring others. Develop training materials.

Basic Qualifications:

• Bachelor's degree required, preferably in Chemistry.

• 1+ year experience in a GMP analytical chemistry lab required.

Additional Skills:

• Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.

• Proficiency with computer systems including Microsoft Office products, LIMS (list other lab systems), etc.

• Ability to working in a lab environment including wearing appropriate PPE and other safety required equipment and considerations.

• Demonstrated strong math and documentation skills.

• Demonstrated strong oral and written communication and interpersonal interaction skills.

Other Information: