Quality Engineer Intern - Summer 2027
Core
Managing multiple projects related to product quality, including design files, risk analysis, CAPA processes, 510k data collection, product testing, and FDA submission documentation.
Role type
Quality Engineer Intern
Builds
Product quality documentation, test plans, and regulatory compliance records for medical devices
Domain
Healthcare / Medical Devices
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Design project experience, risk analysis, CAPA process management, 510k data collection, product testing, documentation authoring, process improvement
Preferred skills
Engineering or Science major, Junior standing, 3.0+ GPA, detail-oriented, organizational skills, analytical skills, problem-solving skills
Technologies
None stated
Responsibilities
Developing test plans to evaluate new and existing products, Authoring Device Master Records and Design Controls, Investigating customer/sales force complaints, Engaging in process improvement activities related to regulatory compliance, Contributing to product design and development for FDA submission, Supporting CAPA's and supplier maintenance
Seniority
Intern