Regulatory Affairs Intern – MedTech Software Submissions

SafeBeat Rx; United States; On-site; USD 20,000 - 30,000; Full time

Job summary

SafeBeat Rx in the United States is looking for a Regulatory Affairs intern to support regulatory activities for software as a medical device. The intern will assist in the compilation of requirements for global regulatory submissions and support file management to meet applicable regulations.

If you are enrolled in a relevant undergraduate or graduate program and want to make a direct impact on patients' lives, we would love to connect with you!

Qualifications

• Enrollment in a scientific, technology, engineering, business, or law-related program.
• Proficient with generating pivot tables and graphs in Excel.
• Ability to work individually and as part of a group.

Responsibilities

• Assist in regulatory submissions for software as a medical device.
• Support file management to meet applicable regulations.
• Participate in project team meetings for strategic discussions.

Skills

US and Global Regulatory Policies Understanding

Microsoft Office

Oral and written communication

Education

Currently enrolled in an undergraduate or graduate program in related fields

Job description

SafeBeat Rx in the United States is looking for a Regulatory Affairs intern to support regulatory activities for software as a medical device. The intern will assist in the compilation of requirements for global regulatory submissions and support file management to meet applicable regulations.

If you are enrolled in a relevant undergraduate or graduate program and want to make a direct impact on patients' lives, we would love to connect with you!