Regulatory Affairs Intern

Johnson & Johnson • Irvine, CA

1d

About The Position

Biosense Webster, Inc., part of Johnson & Johnson’s Medical Devices sector, is recruiting a Regulatory Affairs Intern for its Medical Devices Regulatory Affairs organization in Irvine, California. The internship provides meaningful project experience, exposure to the field, opportunities to learn about the company and network with leadership, and training and mentorship to support educational and career development.

The intern will assist with global regulatory submissions and the transition of files into applicable regulatory and quality databases. The role also includes attending project team meetings with a Regulatory Affairs lead, participating in strategic discussions, learning regulatory affairs competencies related to product registration lifecycle compliance, and evaluating processes to identify potential efficiencies and improvements. Candidates must be enrolled in an accredited college or university and available to work full-time. Start dates are flexible depending on the school schedule.

Requirements

• Be enrolled in an accredited college or university pursuing a bachelor's or master's degree in Life Sciences, Engineering, Law/Legal, or Regulatory Affairs.
• Be available to work full-time.
• Be legally authorized to work in the United States without requiring employment visa sponsorship now or in the future.
• Be detail-oriented and highly organized, with the ability to manage multiple tasks.
• Be able to work independently and as part of a team.
• Be proficient in Microsoft Office, including Word, Excel (with high proficiency in generating pivot tables and graphs), and PowerPoint.
• Have strong oral and written communication skills.

Nice To Haves

• Demonstrated leadership.
• Technical competencies in SharePoint, Teams, and other information technology systems.
• Academic and/or industrial clinical trial experience.
• A minimum GPA of 3.0.
• Participation in campus or community service activities.

Responsibilities

• Assist in compiling and publishing global regulatory submissions for products.
• Support the transition of files to applicable regulatory and quality databases.
• Attend project team meetings with a Regulatory Affairs lead and assist in strategic discussions.
• Develop regulatory affairs competencies to support compliance with product registration lifecycle processes.
• Evaluate current processes and propose opportunities for efficiencies and improvements.

Benefits

• Co-ops and interns may participate in company-sponsored employee medical benefits in accordance with the plan terms.
• Up to 40 hours of sick time per calendar year; Washington State employees may receive up to 56 hours per calendar year.
• Eligibility to participate in the company’s consolidated retirement plan (pension).

What This Job Offers

• Job Type: Full-time
• Career Level: Intern