Engineering Intern

About the Role

Engineering Intern - Summer 2027 at AMETEK provides support for engineering teams focused on the commercialization of medical devices, specifically within the orthopedic industry (hip, knee, and spine segments). Three primary rotations are available: Design & Development, Manufacturing Engineering, and Quality Engineering.

Key Responsibilities

• Support the commercialization of complex new products.
• Under general supervision, conceptualize, design, and develop complex new products.
• Assist in various project aspects including timelines, prototypes, testing, and suppliers.
• Drive problem-solving for design-related issues.
• Research, specify, and recommend materials or alternative solutions.
• Generate documentation per design control procedures.
• Assist in compliance with ISO, FDA, and applicable regulations.
• Support Design for Manufacturability (DFM).
• Support Device Master Record (DMR) development.
• Assist in developing product process flows, including value stream mapping and CTQ (Critical to Quality) flow through.
• Assist in pFEMA (Process Failure Mode and Effects Analysis) development and risk mitigation activities.
• Support Control Plan (CP) development, including inspection methodology, controls, reaction plans, and monitoring.
• Generate engineering test protocols and reports for process characterization and testing.
• Monitor and analyze quality performance for new product development.
• Support device design for inspection.
• Participate in all quality activities associated with new product development.
• Generate gage designs.
• Analyze data to identify trends and improve process quality using statistical analysis.
• Develop sampling rationale.
• Lead special quality projects for continuous improvement.
• May participate in internal and/or supplier audits.
• Special projects as assigned.
• Participation in cadaver studies.
• May be required to train others in similar roles once competency is demonstrated.

Requirements & Tech Stack

• Working toward a bachelor’s degree in Mechanical or Biomedical Engineering preferred.
• Attention to detail required.
• Good written and verbal communication skills required.
• Ability to handle multiple priorities simultaneously.
• Ability to work under direct supervision.
• General understanding of human anatomy required.
• Understand how to apply geometric dimensioning and tolerance (GD&T) required.
• Self-starter/motivator for personal and professional growth.
• 3D CAD modeling experience preferred.
• Microsoft Office (particularly Excel) preferred.

Physical Demands and Work Environment

• Physical demands: Frequently required to stand, walk, sit, use hands to handle objects, reach, stoop, talk, or hear. Specific vision abilities include close vision, color vision, depth perception, and ability to see print in various sizes. May require climbing stairs, kneeling, or crouching. May be required to pull and push up to 15 pounds and occasionally lift boxes up to 25 pounds.
• Work environment: Office environment with a low noise level.