Regulatory Affairs- Internship- Summer 2026

DEKA Research & Development • Manchester, NH

7d

About The Position

The DEKA Research & Development Regulatory Team is seeking a motivated summer intern with an interest in medical device regulation. As a Regulatory Affairs intern you will be immersed in regulatory affairs processes that support the fast-paced and dynamic environment for developing innovative medical device technologies.

As a Regulatory Affairs Intern you will be immersed in the regulatory affairs processes that support many of DEKA’s medical device projects. You will learn about the medical device regulation and focus your work on two specific projects: (1) Develop a standardized system to document the regulatory history across DEKA projects; (2) Development of a process for gathering, assessing, and communicating matters of regulatory intelligence to relevant parties. These projects will teach you about different regulatory processes, device-specific regulatory topics, and how regulatory strategy can be integrated into the medical device development process.

Requirements

• Currently enrolled in an accredited college/institution pursuing Bachelors of Science or Master’s Degree in an Engineering discipline or Regulatory Affairs.
• Demonstrated interest in an FDA-regulated medical device environment
• Strong written and oral communication skills.
• Strong attention to detail.
• Ability to work both independently and in team settings
• Strong interpersonal skills, positive attitude, proactive approach to problem solving, reliable and outcome driven.

Responsibilities

• Develop a company-wide system for documenting regulatory correspondence, developments and activities for a diverse array of medical devices.
• Develop a process for communicating regulatory intelligence to key DEKA personnel.
• Work closely with other RA personnel to learn regulatory processes, strategy and developments across multiple medical device projects in a real-world environment.

What This Job Offers

• Career Level: Intern