Regulatory Affairs Intern

Location
San Francisco

Job Type
Part-time and Full-time

About the role

The Regulatory Affairs intern will support regulatory activities for software as a medical device to develop submissions while interpreting global regulations.

Activities include:

  • Assist in the compilation of requirements for global regulatory submissions (510k, de novo, technical document) of software as a medical device

  • Support the acquisition and management of files to meet applicable regulations (design control/design history files, risk management files, usability files)

  • 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

  • Data analytics specifically from software applications and write ups

Candidate Requirements:

  • US and Global Regulatory Policies Understanding and Shaping activities

  • Currently enrolled full-time in an undergraduate program, or enrolled full-time in a graduate program (M.S., M.E., Ph. D., or M.D.), pursuing a degree majoring in a scientific, technology, engineering, business, or law related field

  • Examples include, biomedical, mechanical, electrical engineering, data analytics/applied statistics, quantitative modeling in biology, pharmacy, life Sciences, medical / scientific writing or public health administration

  • Candidate 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

  • 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

  • Able to work individually, as well as, part of a group, with curiosity and flexibility

  • Possess a “can do” approach, and courage to speak your voice and suggest innovative ideas

Why you should join SafeBeat Rx

At SafeBeat Rx (YC S21), we are building ECG software that saves lives and replaces a hospitalization. By joining our team, you will have a direct impact on millions of patients' lives. Because we focus on medical software, our FDA and go-to-market pathways are much faster than other biotech/medtech startup companies. If our mission and product excite you, we would love to connect.