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Regulatory Intern

Highridge Medical • Westminster, CO, US • 1w ago

Regulatory Intern

Intern

Westminster, CO, US

Yesterday

Requisition ID: 1288

ApplySalary Range:

$21.00 To $21.00 Hourly

Highridge Medical

Highridge Medical creates the world’s most innovative spinal solutions across the spectrum from Motion Preservation to Minimally Invasive Surgery to Core Spine.

Working at Highridge Medical is not just work. Life at Highridge Medical is purpose driven. Every day, you have the privilege of using your talents to demonstrate Confidence in your work and restore Confidence for our patients. Confidence that moves.

Highridge 2026 Summer College Associate Mentor Program (CAMP)

The Highridge Summer CAMP is a paid internship program that has been designed to give students from a variety of backgrounds, universities, and degree programs the opportunity to experience our business firsthand and gain practical skills that can be used in both their academic and future professional endeavors. The individuals who are selected to participate in the program will meet with organizational leaders, participate in leadership learning sessions, and complete a real-world, solution-based, career focused project that will have a meaningful impact on our business.

The Highridge Summer CAMP is scheduled to run between Tuesday, May 26, 2026, and Friday, August 14, 2026. Participants in the program will be expected to:

Be present for the entirety of the program.
Work on-site at our Corporate Headquarters in Westminster, CO.
Work a normal business work week, Monday – Friday, between the normal hours of 8:00 AM – 5:00 PM.

Highly successful interns may be considered for continuing intern opportunities and/or full-time job opportunities.

Job Summary

The Regulatory Intern will aid in maintaining regulatory data for Regulatory Affairs department. This internship is ideal for someone interested in learning about the medical device industry while gaining hands-on experience in clerical and administrative functions. All work will be performed under the guidance of the Regulatory Affairs Manager and senior support staff.

Principal Duties and Responsibilities

Assist with the organization and maintenance of regulatory data and documentation
Perform data entry and cleanup in regulatory tracking systems.
Help prepare submission packets and formatting of regulatory documents.
Maintain electronic and physical filing systems.
Support the migration or integration of data into new systems or platforms Provide general clerical assistance to the Regulatory Affairs team
Participate in all trainings, education opportunities, and community service activities.

This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.