Regulatory Affairs Dev Program – Medical Devices

Abbott (abbottcareers2 board); Santa Clara (CA); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Tuition reimbursement

Education benefits

Job summary

Abbott is a global healthcare leader seeking candidates for the Medical Device Regulatory Affairs Development (RAD) Program. The role involves three 1-year rotations across multiple U.S.

locations, with responsibilities including regulatory submissions, documentation management, and interactions with FDA and other regulatory bodies. Ideal candidates have a life sciences or engineering background and strong communication skills to operate in a fast-paced, matrixed environment.

Qualifications

• Ability to work in a highly matrixed and geographically diverse business environment.
• Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
• Multitasks, prioritizes and meets deadlines in timely manner.

Responsibilities

• Assists in regulatory applications and annual reports to achieve objectives.
• Creates, reviews and approves engineering changes.
• Maintains regulatory submissions and ensures compliance with FDA and worldwide regulations.

Skills

Matrixed environment

Team collaboration

Strong communication

Multitasking

Education

BA/BS in life sciences or engineering

Tools

Regulatory database

SharePoint

Job description

Abbott is a global healthcare leader seeking candidates for the Medical Device Regulatory Affairs Development (RAD) Program. The role involves three 1-year rotations across multiple U.S.

locations, with responsibilities including regulatory submissions, documentation management, and interactions with FDA and other regulatory bodies. Ideal candidates have a life sciences or engineering background and strong communication skills to operate in a fast-paced, matrixed environment.