Medline is looking to build a strong foundation in Quality by providing employees with the knowledge, tools, and experiences they will need to be a successful Quality Engineer at Medline through a two-year development program.
Requirements
- Experience in processing details and understanding and prioritizing their importance to problem solve and draw clear and concise conclusions
- Experience using time management skills such as prioritizing/organizing and tracking details and meeting deadlines of multiple projects with varying completion dates
- Experience using MS Office Suite products (Word, Excel, PowerPoint, Outlook).
Responsibilities
- Providing Quality support throughout the lifetime of a product from design, to launch, to post-market surveillance
- Authoring Device Master Records, Design Controls, Risk Management, protocols, reports, and other critical Quality documentation in compliance with applicable regulations
- Developing test plans to evaluate new and existing products
- Investigate, track, and trend customer and sales force complaints, including generation of trend and Management Review reports
- Communicate significant issues or developments identified during quality assurance activities and provide recommended process improvements to management
- Engaging in process improvement activities related to product quality and regulatory compliance
- Supporting CAPA’s, SCAR’s, supplier maintenance, and more!
Other
- Bachelor's degree required with a minimum 3.0 GPA preferred, senior standing or previously graduated
- Unrestricted permanent US work authorization
