Regulatory Affairs Intern
About The Position
Biosense Webster, Inc., part of Johnson & Johnson’s Medical Devices sector, is recruiting an intern for its Medical Devices Regulatory Affairs organization. Biosense Webster is recognized worldwide for its work in diagnosing and treating cardiac arrhythmias. The internship offers 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 support global regulatory submissions and regulatory/quality file management, participate in project-team discussions, learn regulatory affairs competencies related to product registration lifecycle compliance, and assess processes for potential improvements. Candidates must 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. The role is full-time, with start dates flexible around the school schedule, and is located in Irvine, California. Candidates must be permanently authorized to work in the United States without current or future employment-visa sponsorship.
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; exact start dates are flexible depending on the school schedule.
- 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 with Microsoft Office, including Word, Excel (with strong proficiency 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 the Regulatory Affairs lead and assist in strategic discussions.
- Learn regulatory affairs competencies to support compliance with product registration lifecycle processes.
- Evaluate current processes and propose opportunities for efficiency improvements.
Benefits
- Company-sponsored employee medical benefits, subject to 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).
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What This Job Offers
Job Type
Full-time
Career Level
Intern
