Chemist - QC at Eli Lilly and Company

Indianapolis, Indiana, United States

Eli Lilly and Company Logo
Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, Healthcare, BiotechnologyIndustries

Requirements

  • 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 (preferred)
  • Proficiency with computer systems (LIMS, Empower, Chromeleon, Excel, etc.) (preferred)
  • Proficiency with UHPLC, pH meters, ICPMS, Rad detectors, Dose calibrators, and Gamma detectors, among others (preferred)
  • 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
  • Tasks may require repetitive motion and standing for long periods of time
  • Must be able to lift

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 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 and procedures has occurred and initiates analytical investigations and participates in a Root Cause Investigations
  • Participates, including lead investigator duties, 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

Skills

GMP
analytical testing
sample analysis
data verification
SPV
root cause investigation
laboratory procedures
analytical chemistry
equipment qualification
quality control

Eli Lilly and Company

Develops and delivers prescription medicines globally

About Eli Lilly and Company

Eli Lilly and Company is a global pharmaceutical company that focuses on discovering, developing, and delivering medicines to improve health. The company has a long history of scientific achievements, including the creation of insulin, the first life-saving treatment for diabetes. Lilly's operations involve extensive research and development to create new medications and enhance existing ones, ensuring they are safe and effective. Their products are primarily prescription medicines sold to healthcare providers for various medical conditions, including diabetes, cancer, and pain management. What sets Lilly apart from its competitors is its strong commitment to ethical practices and the protection of its products from counterfeiting. The company's goal is to enhance lives through innovative medical solutions while maintaining high standards of quality and ethics.

Indianapolis, IndianaHeadquarters
1876Year Founded
$1,180.1MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Competition from Novo Nordisk's Ozempic may impact tirzepatide's market share.
Potential construction delays in Indiana could affect GLP-1 drug production timelines.
Regulatory challenges may hinder Kisunla's expansion in new Alzheimer's markets.

Differentiation

Eli Lilly's rich history includes the first life-saving insulin treatment.
Lilly's strategic partnerships enhance its position in neurodegenerative disease treatments.
FDA approval of Zepbound opens new therapeutic markets for sleep disorder treatments.

Upsides

Lilly's $9 billion complex in Indiana boosts GLP-1 drug production capacity.
Kisunla's approval in China expands Lilly's Alzheimer's treatment market in Asia.
Collaboration with EVA Pharma enhances Lilly's reputation as socially responsible.

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