Medical Devices Regulatory Affairs Intern

Wayne State University; Irvine (CA); On-site; USD 32,000 - 72,000; Full time

Job summary

Biosense Webster, Inc., part of Johnson & Johnson, is recruiting an Intern for Medical Devices Regulatory Affairs (MD RA) to gain hands-on experience in regulatory submissions and database management in Irvine, CA. You will work with RA leaders to support project activities and learn essential regulatory competencies.

The role offers mentorship, exposure to global submissions, and opportunities to develop practical skills in a global healthcare company within the Medical Devices sector.

Qualifications

• Pursuing a Bachelor or Master in Life Sciences, Engineering, Law/Regulatory Affairs.
• Full-time availability; start dates flexible to school schedule.
• Authorized to work in the United States; visa sponsorship not needed now or in future.

Responsibilities

• Assist in compiling and publishing global regulatory submissions.
• Support transition of files to regulatory/quality databases.
• Attend project team meetings with RA lead to help collaboration.
• Learn regulatory affairs processes to ensure lifecycle compliance.
• Identify process improvements to increase efficiency.

Skills

Microsoft Office

Pivot Tables

PowerPoint

Written Communication

Education

Life Sciences/Bachelor/Master

Regulatory Affairs/Engineering

Tools

SharePoint

Teams

Excel

Job description

Biosense Webster, Inc., part of Johnson & Johnson, is recruiting an Intern for Medical Devices Regulatory Affairs (MD RA) to gain hands-on experience in regulatory submissions and database management in Irvine, CA. You will work with RA leaders to support project activities and learn essential regulatory competencies.

The role offers mentorship, exposure to global submissions, and opportunities to develop practical skills in a global healthcare company within the Medical Devices sector.