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 is a global healthcare leader seeking a Quality Control Associate to provide technical support for pharmaceutical device testing
Job Summary
Eli Lilly is a global healthcare leader seeking a Quality Control Associate to provide technical support for pharmaceutical device testing.
The role involves investigating quality observations, reviewing GMP laboratory data, and participating in regulatory inspections.
Candidates will receive a comprehensive benefit program including medical, dental, vision, 401(k), and wellness benefits.
Matching Summary
Eli Lilly is a global healthcare leader seeking a Quality Control Associate to provide technical support for pharmaceutical device testing.
Salary
Base: $106,434.00 per year; Bonus/Equity: Eligible for company bonus depending on performance; Benefits: Comprehensive program including 401(k), pension, vacation, medical, dental, vision, life insurance, 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, and EU Medical Device Directive
Nice-to-have
Experience writing requirements documents and training materials
Participation in regulatory agency and internal inspections
Strong root cause analysis skills for quality observations
Ability to perform impact analyses for change management
Key Requirements
Bachelor's degree in Biotechnology, Biomedical Engineering, or closely related field
Minimum 1 year of experience with quality control operations for parenteral or dry products
1 year of experience with analytical lab equipment including Zwick, CADI, and MicroVu
1 year of experience with documentation management systems like Veeva and Quality Docs
1 year of experience with quality systems and regulatory requirements (CGMP, 21 CFR 820, ISO13485)