Intern - Device Development Engineering

Role Summary

Intern - Device Development Engineering. Participate in the design, development, verification and validation of combination products in support of Teva’s global R&D pipeline with focus on parenteral delivery of biologics and biosimilars. Learn regulations, directives, guidelines and standards relevant to the products and collaborate with a global team of developers to impact patient lives. Location: West Chester, PA. Length: 12 weeks. Schedule: 40 hours/week for 12 weeks in Summer 2026.

Responsibilities

• Contribute to user needs and product requirements, specifications, verification and validation plans and reports.
• Create or modify SolidWorks solid models and drawings.
• Support development of analytical models and simulations.
• Design, develop, and prototype lab fixtures and equipment for product performance assessment.
• Establish test protocols and methods to challenge functionality through robustness testing and Design of Experiments (DoE).
• Lead the development of 3D printed or machined rapid prototype models.
• Participate in small quantity builds and execute testing.
• Collaborate with human factors engineers on early usability assessments and formative and summative validation studies.

Qualifications

• Currently enrolled in undergraduate or graduate program in Mechanical or Biomedical Engineering or related discipline.
• Excellent verbal and written communication skills.
• Self-motivated and able to work collaboratively in a team environment.
• Experience with SOLIDWORKS, MATLAB, Minitab, Instron, and other lab equipment is preferred but not required.