Medline is looking for a Quality Intern to manage multiple projects related to product quality, including Design Files, Risk Analysis, CAPA process, 510k data collection, product testing, and creating documentation for the Master Device Record.
Requirements
- Design project experience
Responsibilities
- Developing test plans to evaluate new and existing products
- Authoring Device Master Records, Design Controls, protocols, reports, and other critical Quality documentation
- Investigating customer/sales force complaints and assuring files are addressed and closed on time
- Engaging in process improvement activities related to product quality and regulatory compliance
- Contributing to product design and development, including generation of documentation required for submission to the FDA
- Supporting CAPA’s, SCAR’s, supplier maintenance, risk analysis, and more!
Other
- Engineering or Science related majors preferred
- Junior standing with 3.0 minimum GPA preferred
- Detail oriented with superior organizational, analytical, and problem-solving skills
- Motivated self-starter
- Good documentation skills and an attention to detail
- Unrestricted permanent US work authorization
