About The Position
This internship focuses on supporting the design control documentation and design activities for multiple complex generic projects within the R&D Scientific Affairs department. Interns will also gain exposure to project management activities. The role provides an opportunity to learn about the design and development of medical devices, interact with cross-functional teams, understand the regulatory landscape, and develop device compliance documents.
Requirements
- Current full-time enrollment in an accredited college or university undergraduate or graduate program in Human Resources, Business Administration, Psychology, or a related field
- Minimum cumulative GPA of 3.0
- Must be at least 18 years old
- Must be legally authorized to work in the United States
- Must commit to the full duration of the internship (June 1, 2026 - August 28, 2026)
Nice To Haves
- Bio-medical engineer
- Mechanical engineer
- Design
- Plastics
- Medical device development
- CAD modelling
- MATLAB
Responsibilities
- Support design control documentation of multiple complex generics projects (50%)
- Support design activities on 3 projects (30%)
- Support project management activities on 3 projects (20%)
Benefits
- Paid internships
- Rates starting at $20/hr
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What This Job Offers
Job Type
Full-time
Career Level
Intern
Education Level
High school or GED
Number of Employees
1,001-5,000 employees
