Medical Device Regulatory Affairs Development (RAD) Program (on-site)
Abbott Laboratories
About this role
Abbott offers a role within their Medical Device Regulatory Affairs Development Program, providing rotation-based experience in regulatory submission processes, compliance, and communication with regulatory agencies. The position supports global product registration activities and ensures adherence to international regulations in a dynamic healthcare environment.
Skills
About Abbott Laboratories
abbott.comInnovative medical devices and health care solutions for cardiovascular health, diabetes management, diagnostic testing, nutrition, chronic pain and more.
Recent company news
AIA Group Ltd Raises Position in Abbott Laboratories $ABT
7 hours ago
Pharmaceutical companies move away from horseshoe crab biomedical testing
2 days ago
Abbott Laboratories revenue 2004-2025
1 week ago
Hilltop Holdings Inc. Acquires 83,190 Shares of Abbott Laboratories $ABT
3 days ago
Mairs & Power Inc. Decreases Stock Holdings in Abbott Laboratories $ABT
2 days ago
About Abbott Laboratories
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Leadership Team
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
Unlock Company Insights
View leadership team, funding history,
and employee contacts for Abbott Laboratories.
Salary
$74k – $116k
per year
More jobs at Abbott Laboratories
Similar Jobs
Senior Regulatory Affairs Manager
Novartis
Assoc Regulatory Affairs Spec
Collabera
Regulatory Affairs Specialist
Integrated Resources INC
Senior Regulatory Affairs Specialist Medical device
United States Postal Service
Principal Regulatory Affairs Specialist
Cardinal Health
Regulatory Affairs Specialist II
Arizona State Jobs