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Medical Device Regulatory Affairs Development (RAD) Program at Abbott Laboratories - ApplyBlast

Medical Device Regulatory Affairs Development (RAD) Program

Abbott Laboratories

2 months ago

3.7 on Glassdoor

Santa Clara, California, United States

Onsite

Full Time

Trainee

0 applicants

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About this role

The Medical Device Regulatory Affairs Development (RAD) Program offers a rotational opportunity across multiple U.S. locations, focusing on regulatory registration, compliance, and product market entry for medical devices. Participants will engage in specialized work assignments, including the preparation and submission of regulatory documentation, review of engineering changes, and support for global product release processes. The role requires collaboration with internal teams and regulatory agencies to ensure adherence to FDA and international standards.

Responsibilities

Prepare and submit regulatory applications and documentation for medical device registration
Review and analyze regulatory guidelines to ensure compliance with FDA and international standards
Support product release processes and maintain regulatory databases and file systems

Skills

Qualifications

BA or BS degree in life sciencesBA or BS degree in engineering

About Abbott Laboratories

abbott.com

Innovative medical devices and health care solutions for cardiovascular health, diabetes management, diagnostic testing, nutrition, chronic pain and more.