Five years industry experience in quality or manufacturing
Eli Lilly UK is seeking a Quality Assurance professional to support their Product Complaint Handling and Medical Device Reporting Processes. The ideal candidate will have experience in quality, technical services, or manufacturing operations, and possess strong analytical and communication skills
Job Summary
This role supports product complaint handling and medical device reporting processes while driving practical change across the organization.
The successful candidate will act as a Data Steward for complaint data and represent Indianapolis Device Manufacturing at inspections and audits.
Lilly offers a comprehensive benefit program including medical, dental, vision, 401(k), pension, and flexible benefits to eligible employees.
Matching Summary
Match Score: 85
Eli Lilly UK is seeking a Quality Assurance professional to support their Product Complaint Handling and Medical Device Reporting Processes. The ideal candidate will have experience in quality, technical services, or manufacturing operations, and possess strong analytical and communication skills.
Salary
Base: $126,000 - $204,600; Bonus/Equity: Eligible for company bonus; Benefits: Comprehensive program including 401(k) and medical
Skills & Requirements
Must-have
GMP document authoring and approval
Regulatory compliance knowledge cGMP ISO13485
Five years industry experience in Quality or Manufacturing
Complaint handling and device safety reporting
Trend analysis and data visualization skills
Nice-to-have
Experience with Six Sigma methodology
Mentoring and coaching junior staff
Advanced Excel and SQL querying skills
Power BI or Tableau dashboarding experience
Cross-functional stakeholder collaboration
Key Requirements
Bachelor's degree in Engineering, Medical, or Life Sciences
Minimum five years of industry related experience
Technical knowledge in design, manufacturing, and validation
Knowledge of regulatory requirements like 21 CFR 820