Quality Control Associate (r1-r3)

Eli Lilly and Company

Indianapolis, IN, US
Base: $106,434.00 py; bonus/equity: eligible for c...
Bachelor's degree in biotechnology or related field
1 year experience with quality control laboratory operations
Experience with parenteral products or pharmaceutical devices
Eli Lilly and Company seeks a dedicated professional to provide technical support for pharmaceutical device testing and ensure life-changing medicines reach those who need them

Job Summary

  • Eli Lilly and Company seeks a dedicated professional to provide technical support for pharmaceutical device testing and ensure life-changing medicines reach those who need them.
  • The role involves comprehensive review of lot release testing data, investigating deviations using root cause analysis, and supporting change management processes.
  • Candidates will benefit from a comprehensive benefit program including medical, dental, vision, 401(k), pension, and various well-being initiatives.

Matching Summary

Eli Lilly and Company seeks a dedicated professional to provide technical support for pharmaceutical device testing and ensure life-changing medicines reach those who need them.

Salary

Base: $106,434.00 per year; Bonus/Equity: Eligible for company bonus depending on performance; Benefits: Comprehensive program including 401(k), pension, medical, dental, vision, vacation, and well-being benefits

Skills & Requirements

Must-have

  • Bachelor's degree in Biotechnology or related field
  • 1 year experience with quality control laboratory operations
  • Experience with parenteral products or pharmaceutical devices
  • Proficiency with Zwick, CADI, and MicroVu analytical equipment
  • Knowledge of Veeva and Quality Docs documentation systems
  • Understanding of CGMP, 21 CFR 820, ISO13485 regulations

Nice-to-have

  • Root cause analysis skills for quality observations
  • Experience writing requirements documents and training materials
  • Participation in regulatory agency inspections
  • Ability to perform impact analyses for change management
  • Willingness to travel up to 5% domestically and internationally

Key Requirements

  • Bachelor's degree in Biotechnology, Biomedical Engineering, or closely related field
  • Minimum 1 year experience with quality control operations for parenteral/dry products/devices
  • 1 year experience with analytical lab equipment (Zwick, CADI, MicroVu)
  • 1 year experience with documentation management systems (Veeva, Quality Docs)
  • 1 year experience with quality systems and regulatory requirements (CGMP, 21 CFR 820, ISO13485)

Work Rights

Not specified

Tailored Resume

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