Medical Device Compliance Manager

3 weeks ago


Saint Paul, Minnesota, United States Collabera Full time
Company Overview

Collabera is a Global Digital Solutions Company providing Software Engineering Solutions for the world's most tech-forward organizations.

Job Description

This role involves leading project submissions for regulatory approvals and acting independently to identify and resolve problems. The ideal candidate will have advanced regulatory expertise, strategic thinking, and creativity in support of programs.

Responsibilities
  • Lead project submissions for regulatory approvals
  • Apply advanced regulatory expertise to guide cross-functional partners
  • Demonstrate strategic thinking and creativity in support of programs
  • Provide regulatory affairs project management for various areas
Requirements
  • Bachelor's degree in a medical, science, or engineering-related discipline
  • 8 years of experience in the medical device industry, with 5 years related to FDA and EU MDR submissions
  • Ability to work effectively on project teams
Benefits
  • Competitive salary: $120,000 - $180,000 per year
  • Opportunities for career growth and professional development


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