Regulatory Intern

Job Summary

Highridge Medical creates the world’s most innovative spinal solutions across the spectrum from Motion Preservation to MIS to Bone Healing 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.

We are seeking a detail-oriented and motivated student to join our Regulatory Affairs team as a summer intern. This internship is ideal for someone interested in learning about the medical device industry while gaining hands-on experience in clerical and administrative functions.

Principal Duties And Responsibilities

• Assist with the organization and maintenance of regulatory documentation and files
• 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 audit preparation and archiving activities
• Provide general clerical assistance to the Regulatory Affairs team
  
  

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.

Skills

Expected Areas of Competence (i.e. knowledge, skills, and abilities)

• Current undergraduate student (preferably in life sciences, healthcare, business, or related field)
• Strong attention to detail and organizational skills
• Proficient in Microsoft Office (especially Word and Excel); familiarity with SharePoint a plus
• Ability to manage time effectively and follow instructions
  
  

What You’ll Gain

• Insight into the role of documentation and recordkeeping in product lifecycle management
• Experience working in a professional and collaborative office environment
• Opportunities for mentorship and career development
  
  

Travel Requirements

• N/A