What are the responsibilities and job description for the Chemist - Quality Control position at Eli Lilly?
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.
Position Brand Description :
The Chemist - QC - IAPI performs accurate and timely testing of routine and investigative lab samples in accordance with appropriate GMP and safety guidelines. The Chemist - QC - IAPI also participates in second person verification (SPV) of analytical data, laboratory investigations, equipment calibrations and maintenance by executing well-defined protocols and procedures. The Chemist - QC - IAPI identifies, communicates, and owns opportunities for improvement within the lab. The Chemist - QC - IAPI utilizes technical skills to perform in-depth problem solving, proactively identify opportunities for continuous improvement, and complete thorough investigations of atypical data and results. Outcomes of these activities including results, conclusions, and action plans and / or technical documents.
The position is also responsible for technical mentoring of laboratory staff and sharing technical information and best practices within the work group and across plant sites. The Chemist - QC - IAPI participates and influences the technical agenda of the plant or corporation.
Key Objectives / Deliverables :
Sample Analysis and Reporting
- Accurately and safely perform analytical test methods or related support activities (such as Forensic Investigations) as per procedures or protocols and reviews that results conform to standards.
- Perform data entry and reviews own work for accuracy in accordance with laboratory procedures, standards, and GMP requirements.
- Recognizes when a deviation from procedures has occurred and initiates an investigation.
- Verify (SPV) analytical data of other analysts within the lab as required.
Continuous Improvement Initiatives
Lab Operations
Basic Requirements :
Additional Preferences :
Other Information :
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