Regulatory Intern

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. Expected Areas of Competence (i.e. knowledge, skills, and abilities) Proficient in Microsoft Office Suite, focused heavily in Excel and SharePoint. Familiarity with medical device, orthopedic, or biomechanics content is a plus Strong attention to detail and ability to identify trends in data sets Strong written and verbal communication skills. Ability to tolerate ambiguity, handle multiple priorities, and identify creative solutions to complex problems. Ability to take initiative, meet commitments, and create new tools or solutions to achieve business results. Strong interest in healthcare, medical devices, or orthopedics preferred. Education/Experience Requirements Students currently enrolled in a college or university program who are working towards a bachelor's or master's degree in engineering, management, business administration, communications, or related field. Travel Requirements N/A Highridge Medical is an equal opportunity employer committed to diversity and inclusion in the workplace. All qualified applicants for employment and employment decisions are considered and evaluated without regard to race, color, religion, national origin, age, gender, sex (including pregnancy, childbirth, related medical conditions, lactation and breastfeeding), gender identity or expression (including transgender status), sexual orientation, marital status, military status, protected veteran status, disability, protected medical condition as defined by applicable state or local law, genetic information, or any other status protected under applicable federal, state, and local laws.

Created: 2026-03-10