Medline is looking to add new talent to support its continued growth and build a strong foundation in Quality by providing employees with the knowledge, tools, and experiences they will need to be a successful Quality Engineer.
Requirements
- Experience using MS Office Suite products (Word, Excel, PowerPoint, Outlook)
- 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
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
- Collaborate with Regulatory, R&D, Product Managers, Manufacturing, Operations, and other cross functional groups
- 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
Other
- Bachelor's degree required with a minimum 3.0 GPA preferred, senior standing or previously graduated
- Unrestricted permanent US work authorization
- Ability to work 30 or more hours per week on average
- Ability to prioritize and organize multiple projects with varying completion dates
- Ability to communicate effectively with cross-functional groups
