Regulatory Affairs Intern — MedTech & Devices

Regulatory Jobs; Irvine (CA); On-site; USD 32,000 - 72,000; Full time

Job summary

Biosense Webster, Inc., part of Johnson & Johnson, is recruiting for an Intern in Medical Devices Regulatory Affairs (MD RA) in Irvine, CA. This internship offers mentorship, project exposure, and global regulatory experience within the Medical Devices Regulatory Affairs organization.

You will support regulatory submissions, database transitions, and cross-team collaboration while gaining hands-on regulatory knowledge across the product lifecycle in a global healthcare environment.

Qualifications

• Enrolled in accredited college/university pursuing Bachelor or Master degree in Life Sciences, Engineering, Law/Legal or Regulatory Affairs.
• Available to work Full-time with flexible start dates depending on school schedule.
• Legally authorized to work in the United States without sponsorship now or in the future.
• Demonstrated leadership is preferred.
• Detail-oriented, highly organized, able to manage multiple tasks.
• Able to work independently as well as on a team.
• Proficient with Microsoft Office, Word, Excel (pivot tables/graphs), PowerPoint; SharePoint/Teams desirable.
• Academic/industrial clinical trial experience preferred.
• Minimum GPA of 3.0 preferred.
• Campus/community service participation desired.

Responsibilities

• Assist in compiling and publishing global regulatory submissions for products.
• Support transition of files to regulatory/quality databases.
• Attend project team meetings with RA lead to aid in strategy discussions.
• Learn regulatory affairs competencies for product registration lifecycle compliance.
• Evaluate current processes and propose efficiency improvements.

Education

Bachelor's or Master in Life Sciences, Engineering, Law/Legal, or Regulatory Affairs

Tools

Microsoft Office Suite

Word

Excel

PowerPoint

SharePoint

Teams

Job description

Biosense Webster, Inc., part of Johnson & Johnson, is recruiting for an Intern in Medical Devices Regulatory Affairs (MD RA) in Irvine, CA. This internship offers mentorship, project exposure, and global regulatory experience within the Medical Devices Regulatory Affairs organization.

You will support regulatory submissions, database transitions, and cross-team collaboration while gaining hands-on regulatory knowledge across the product lifecycle in a global healthcare environment.