(#R-103940) Regulatory Affairs Intern at Johnson & Johnson

Wayne State University; Irvine (CA); Vor Ort; USD 32.000 - 72.000; Vollzeit

Zusammenfassung

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.

Qualifikationen

• 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.

Aufgaben

• 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.

Kenntnisse

Microsoft Office

Pivot Tables

PowerPoint

Written Communication

Ausbildung

Life Sciences/Bachelor/Master

Regulatory Affairs/Engineering

Tools

SharePoint

Teams

Excel

Jobbeschreibung

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At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function

Career Programs

Job Sub Function

Non-LDP Intern/Co-Op

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Category

Career Program

All Job Posting Locations

Irvine, California, United States of America

Job Description

Biosense Webster, Inc., part of the Medical Devices sector withinJohnson & Johnson, is recruiting for an intern for itsMedical Devices Regulatory Affairs organization.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/ .

Biosense Webster, Inc. is recognized worldwide as a leader in the science behind the diagnosis and treatment of cardiac arrhythmias.

The internship experience gives you the opportunity to shine and share your knowledge, energy, and passion on meaningful projects that impact people all over the world. In addition to projects that will provide maximum experience and exposure in your desired field our team provides opportunities to learn more about the company, network with leadership, and develop the skills needed to succeed in a global organization.

The Intern –Medical Devices Regulatory Affairs (MD RA)opportunity will help you grow in your educational and career development, and we will provide training and mentorship as you hone your skills and build confidence in the healthcare field. During this internship, you will also have an opportunity to:

• Assist in the compilation and publishing of global regulatory submissions of our products
• Support the transition of files to applicable regulatory/quality databases
• Attend project team meetings with RA lead to assist in strategic discussions to hone team collaboration skillset
• Learn regulatory affairs competencies to ensure product registration lifecycle processes compliance
• Evaluate current processes and propose opportunities for efficiencies/improvements

Qualifications

• Candidates must be enrolled in an accredited college/university pursuing a Bachelor or Master degree in one the following areas:Life Sciences, Engineering, Law/Legal, and Regulatory Affairs.
• Candidates must be available to work Full-time. Exact start dates are flexible depending on school schedule.
• Candidates must be legally authorized to work in the United States and not require sponsorship for employment visa status (e.g. H1-B status) now or in the future.
• Demonstrated leadership is preferred.
• Candidates must be detail-oriented, highly organized and able to manage multiple tasks.
• Candidates must have the ability to work independently as well as on a team.
• Candidates need to be proficient with Microsoft Office, Word, Excel (including a high proficiency with generating pivot tables and graphs), and Power Point, and have strong oral and written communication skills. Additional technical competencies in SharePoint, Teams and other information technology systems are highly desirable.
• Candidates with academic and/or industrial clinical trial experience are strongly preferred.
• A minimum G.P.A. of 3.0 is strongly preferred.
• Participation in campus/community service activities is desired.

The anticipated base pay range for this position is :

$23.50/hr to $52.50/hr

Additional Description for Pay Transparency

The expected pay range for this position is between $23.50 per hour and $52.50 per hour but will be based on candidate's program year, discipline, degree and/or experience. Co-Ops/Interns are eligible to participate in Company sponsored employee medical benefits in accordance with the terms of the plan. Co-Ops and Interns are eligible for the following sick time benefits: up to 40 hours per calendar year; for employees who reside in the State of Washington, up to 56 hours per calendar year. Co-Ops and Interns are eligible to participate in the Company’s consolidated retirement plan (pension). For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits This job posting is anticipated to close on [8/27/2027]. The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.