Job Description:

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Cerenovus, Inc., part of the Medical Devices sector within Johnson & Johnson, is recruiting for an intern/Co-op for its Medical Devices Regulatory Affairs organization. At CERENOVUS, we are proud to be on the front lines of stroke care – where every second counts – and strive to give patients a new lease on life after stroke.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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/.

The internship/Co-op 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/Co-op – 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
  

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Qualifications

• Candidates must be enrolled in an accredited college/university pursuing a Graduate degree (either Master's or PhD) in one of 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.
• A minimum G.P.A. of 3.0 is strongly preferred.

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