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Chemist - QC - FDE

Eli Lilly and Company

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Location: Indianapolis, IN Posted Date: 4/15/2013 Position Type: Full time Job Code: ELY3069BRBS Required Education: Bachelors Degree Areas of Expertise Desired: Quality Control

Description

Company Description:
Lilly is the 10th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 135 years. Across the globe, we are a leader in investing in research and development and we also invest in our employees – in competitive salaries, training and development, and health.
The pharmaceutical industry is a complex, rapidly changing environment and we are looking for highly capable leaders to help us continue bringing innovation to patients.
If you are interested in being considered for employment at Lilly, we encourage you to review the following opportunity:

Job Description:
The chemist performs accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. The chemist completes second person verification of results. The chemist also participates in laboratory root cause 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 practice with group. This position is a Fixed Duration Position.

Key Objectives/Deliverables:
•   Verify analytical data within the lab as requested.
•   Accurately and safely perform analytical test methods or related support activities as per procedure or protocols.
•   Use technical knowledge in the review and interpretation of data for conformance to procedures, standards and protocols and/or real time recognition of aberrant data results.
•   Perform data entry and review of own work for accuracy in accordance with laboratory procedures, standards and GMP requirements.
•   Recognizes when a deviation from procedures, etc has occurred and initiates and participates in a Root Cause Investigation.
•   Troubleshoot 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.
•   Contribute to development of laboratory quality reviews.
•   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.
•   Comply with and implement safety standards.
•   Executes notification to management when required by procedures or standards. Initiate change controls and deviations.
•   Train and mentoring others.
•   Develop training materials.

Requirements

Basic Qualifications
•   Bachelor degree in a science field related to the lab or 7-10 years of relevant experience in a GMP lab.
•   Responsible for maintaining a safe work environment, working safely and accountable for supporting all Health, Safety and Environmental Corporate and Site Goals.
•   Demonstrated proficiency with HPLC
•   Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position

Additional Skills/Preferences
•   Proficiency with computer systems including Microsoft Office products, Empower, Smartlab and Trackwise.
•   Ability to multitask and manage time effectively.
•   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.

Additional Information
•   Tasks may require repetitive motion and standing for long periods of time.
•   Overtime or weekend work may be required.
•   Required to wear a pager off shift and respond to issues.
•   Day shift Monday- Friday, 8hours a day Minimal travel required, if any.
•   Some allergens are present in the Parenteral Plant.
•   Mobility requirements and exposure to allergens should be considered when applying for this position
•   Background check is required.

This is not a permanent position. Fixed duration employment of up to four years

ELI LILLY AND COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER
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