Analyst – Qc Chemistry & Device

Lilly

Indianapolis, Indiana, US
Base: $65,250 - $169,400; bonus/equity: compyny bo...
Gmp qc laboratory environment
Analytical testing and data documentation
Laboratory investigations
The Analyst – QC Chemistry & Device performs accurate and timely laboratory testing and second person verification (SPV) of analytical data in accordance with applicable GMP, regulatory, and safety requirements to support site production and stability needs

Job Summary

  • The Analyst – QC Chemistry & Device performs accurate and timely laboratory testing and second person verification (SPV) of analytical data in accordance with applicable GMP, regulatory, and safety requirements to support site production and stability needs.
  • Key Objectives include independently performing accurate and timely analytical testing, performing second person verification (SPV) and peer review of analytical data, and executing laboratory testing techniques including HPLC, UV-Vis, Capillary Electrophoresis (CE), device testing, compendial testing, and utilities testing.
  • Full-time equivalent employees are eligible for a company bonus, a comprehensive benefit program including 401(k), pension, vacation, medical, dental, vision, and more.

Matching Summary

The Analyst – QC Chemistry & Device performs accurate and timely laboratory testing and second person verification (SPV) of analytical data in accordance with applicable GMP, regulatory, and safety requirements to support site production and stability needs.

Salary

Base: $65,250 - $169,400; Bonus/Equity: company bonus; Benefits: comprehensive benefit program

Skills & Requirements

Must-have

  • GMP QC laboratory environment
  • analytical testing and data documentation
  • laboratory investigations
  • HPLC, UV-Vis, CE testing
  • night shift team contributor

Nice-to-have

  • strong attention to detail
  • ability to work independently
  • collaborate across shifts
  • lean lab and 5S concepts

Key Requirements

  • Bachelor's degree in Chemistry, Biology, Microbiology, or related scientific discipline
  • Demonstrated experience in GMP QC laboratory
  • Experience performing work with minimal supervision
  • Experience supporting manufacturing or stability testing
  • Experience with LIMS and Empower
  • Hands-on experience with HPLC, CE, device testing, compendial methods
  • Experience performing second person verification (SPV)
  • Working knowledge of FDA regulations, cGMP, compendial requirements
  • Experience participating in laboratory investigations, root cause analysis, CAPA activities
  • Familiarity with Veeva Vault QMS or similar electronic quality management systems

Work Rights

Not specified

Tailored Resume

Cover Letter