Regulatory Affairs Intern - Remote

Overview

The RA Intern provides support for a variety of Regulatory Affairs activities related to global registrations or RA projects, assisting multiple professionals across different product lines to ensure compliance with global regulatory requirements.

In Short

• Support Regulatory Affairs activities and projects.
• Assist with regulatory submissions and documentation.
• Manage multiple competing priorities in a regulated environment.
• Collaborate with subject matter experts.
• Work with Microsoft Office and internal software programs.
• Detail-oriented and methodical approach to project work.
• Ability to work independently with minimal supervision.
• Good problem-solving and analytical skills.
• Strong written and oral communication skills.
• Currently enrolled in or recently graduated from an undergraduate or graduate program.

Requirements

• High school diploma or equivalent required.
• Strong organizational skills.
• Ability to summarize scientific and technical data.
• Experience in a team-oriented and fast-paced environment.
• Ability to review and collate project-related documentation.
• Good communication and interpersonal skills.
• Experience with auditing and publishing regulatory submissions preferred.
• Detail-oriented with a high degree of accuracy.

Benefits

• Opportunity to learn and grow in a global medical technology company.
• Supportive work environment.
• Encouragement to bring your authentic self to work.
• Engagement in meaningful projects that impact health.
• Collaboration with diverse teams.
• Potential for flexible work arrangements.