Regulatory Affairs Associate — Global Submissions

Medtronic; Mounds View (MN); On-site; USD 61,000 - 91,000; Full time

Benefits offered by this job

Health, Dental and Vision Insurance

Tuition assistance/reimbursement

401(k) plan with employer match

Life insurance

Well-being program

Job summary

Medtronic is seeking an Associate Regulatory Affairs Specialist in Minneapolis, MN. The role involves supporting international submissions, regulatory operations, and project coordination.

You will work under guidance to maintain regulatory approvals and manage listing data, among other duties, contributing to global regulatory excellence. Ideal candidates have a Bachelor’s degree and strong technical writing skills, with experience in medical devices.

Qualifications

• Bachelor's degree 0 years of regulatory affairs or related experience.

Responsibilities

• Understand global regulatory requirements and how to research detailed requirements.
• Contribute to global product registration maintenance, including EU MDR Technical Documentation/MDD Technical Files.
• Assess device changes for registration implications and notify geographies of regulatory changes.

Skills

Regulatory affairs

Technical writing

Project coordination

Regulatory submissions

Education

Bachelor's degree

Tools

Excel

PowerBI

Word processing

Job description

Medtronic is seeking an Associate Regulatory Affairs Specialist in Minneapolis, MN. The role involves supporting international submissions, regulatory operations, and project coordination.

You will work under guidance to maintain regulatory approvals and manage listing data, among other duties, contributing to global regulatory excellence. Ideal candidates have a Bachelor’s degree and strong technical writing skills, with experience in medical devices.