ApplyBlast uses AI to match you with the right jobs, tailor your resume and cover letter, and apply automatically so you can land your dream job faster.

Features

Auto Apply Resume Optimizer Cover Letter Optimizer Interview Prep

Company

Social Media

Need Help?

team@applyblast.com

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

Plymouth, Minnesota, United States

Onsite

Full Time

Trainee

0 applicants

View Job Listing

Apply to 100+ jobs

About this role

The Medical Device Regulatory Affairs Development (RAD) Program offers a rotational opportunity across multiple US locations, focusing on regulatory registration, compliance, and product market entry for medical devices. The role involves preparing regulatory applications, reviewing engineering changes, and maintaining global regulatory databases to ensure adherence to FDA and international standards. Participants will support product release processes and interface with regulatory agencies to facilitate successful product launches.

Responsibilities

Prepare and submit regulatory documentation for medical device registration and compliance
Review and analyze regulatory guidelines and engineering changes for FDA and international agencies
Maintain regulatory databases and support global product release processes

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.