Intern - Device Development Engineering

As a Device Development Engineering Intern in Teva's West Chester R&D Devices group, you will participate in the design, development, verification and validation of combination products in support of Teva’s global R&D pipeline with special focus on the parenteral delivery of biologics and biosimilars. You will gain knowledge of the regulations, directives, guidelines and standards relevant to the combination products on which you contribute. You will be exposed to a global team of biologics and combination products developers who are motivated by the opportunity to have a positive impact on patient’s lives.

Location: Onsite at our West Chester, PA campus.

Length: 12 weeks

Schedule: You must be available to work a 40-hour work week for 12 weeks during the summer of 2026.

Essential Duties & Responsibilities:

• Contribute to user needs and product requirements, specifications, verification and validation (V&V) 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 (HF) engineers on early usability assessments and formative and summative validation studies.

Qualifications

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