A company is looking for a Quality Engineer to support post-market projects related to medical devices.
Key Responsibilities
Support post-market updates and maintenance of risk documentation
Assist in design change evaluations and complaint investigations
Work on high-quality impacting projects within the Sustaining Quality Engineering team
Required Qualifications
2+ years of Quality Engineering experience, preferably in Medical Device Manufacturing or other regulated industries
Experience in executing tasks for projects, risk review, and CAPA
Familiarity with risk assessment review and inspection plan creation
Knowledge of documentation change management and project management
Strong work ethic and ability to work independently
Quality Engineer • Rockford, Illinois, United States