Tara Burrell

Senior Regulatory Affairs Specialist

Role
Senior Regulatory Affairs Specialist at Bracco Medical Technologies
Location
Minneapolis, MN, US
LinkedIn followers
500 followers
Healthcare & Human ServicesView LinkedIn profile

About Tara Burrell

Dedicated, knowledgeable and reliable Regulatory Affairs and Quality Assurance professional working in a medical device company where I am able to utilize my FDA and EU CE marking submission experience, my contributions to new product development teams, my experience in developing new and challenging regulatory strategies, with successful outcomes, and my proven ability to deliver.14 years of medical device regulatory and quality experience with a focus on technical writing in various forms including scientific rationale, justifications, test methods, test protocols, and test reports.

Experience

  1. Senior Regulatory Affairs Specialist

    Bracco Medical Technologies

    Apr 2025 — Present · Eden Prairie, MN, US

Skills

  • Regulatory Requirements
  • Healthcare
  • Project Management
  • Cross-Functional Team Leadership
  • Iso 14971
  • Glp
  • Product Launch
  • Fda Gmp
  • Biocompatibility
  • 21 Cfr
  • Market Development
  • Part 820
  • Management
  • Manufacturing
  • Iso
  • Pharmaceutical Industry
  • Strategic Planning
  • R
  • Capital Equipment
  • Product Development

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Tara Burrell — Senior Regulatory Affairs Specialist at Bracco Medical Technologies in Minneapolis, MN, US | Unifers