Quality Control Associate (r1-r3)

Eli Lilly UK

Indianapolis, IN, US
Base: $106,434.00 py; bonus/equity: compyny bonus ...
Quality control laboratory operations
Pharmaceutical device testing
Root cause analysis for quality deviations
Eli Lilly and Company seeks a Quality Control Associate (R1-R3) to provide technical support for pharmaceutical device testing and quality control operations

Job Summary

  • Eli Lilly and Company seeks a Quality Control Associate (R1-R3) to provide technical support for pharmaceutical device testing and quality control operations.
  • The position offers a comprehensive benefit program including 401(k), pension, medical, dental, vision, life insurance, and well-being benefits.
  • Lilly is dedicated to diversity, equal opportunity employment, and offers accommodations for individuals with disabilities during the application process.

Matching Summary

Eli Lilly and Company seeks a Quality Control Associate (R1-R3) to provide technical support for pharmaceutical device testing and quality control operations.

Salary

Base: $106,434.00 per year; Bonus/Equity: Company bonus eligible; Benefits: Comprehensive benefits including 401(k), pension, medical, dental, vision, life insurance, and wellness programs

Skills & Requirements

Must-have

  • quality control laboratory operations
  • pharmaceutical device testing
  • root cause analysis for quality deviations
  • Good Manufacturing Practices (GMP) compliance
  • documentation management systems
  • analytical lab equipment operation
  • regulatory requirements adherence

Nice-to-have

  • participation in regulatory inspections
  • change management support
  • technical report review
  • training material development
  • employee resource group involvement

Key Requirements

  • Bachelor’s degree in Biotechnology or related field
  • 1 year experience in quality control laboratory operations
  • 1 year experience with parenteral, dry products or pharmaceutical devices
  • 1 year experience writing requirements and training materials
  • 1 year experience with Zwick, CADI, MicroVu lab equipment
  • 1 year experience with Veeva and Quality Docs systems
  • 1 year experience with CGMP, 21 CFR 820, ISO13485, EU Medical Device Directive compliance

Work Rights

Not specified

Tailored Resume

Cover Letter