Advanced Regulatory Affairs Associate (Albertville)

3M in Albertville, MN

  • Industry: Executive Management - Marketing/Public Relations
  • Type: Full Time
  • $140,350.00 - 140,350.00
position filled

Position Description

Advanced Regulatory Affairs Associate

Collaborate with Innovative 3Mers Around the World

Choosing where to start and grow your career has a major impact on your professional and personal life, so its equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a diversity of people, global locations, technologies and products, 3M is a place where you can collaborate with 93,000 other curious, creative 3Mers.

Ive seen firsthand how 3M is a place where curious, creative and collaborative people thrive and build a rewarding career. As a leader in this company, my goal is to ensure each 3Mer sees and feels the positive impact theyre making around the world, and that they know theyre valued. Kristen Ludgate, senior vice president of Human Resources at 3M

The Impact Youll Make in this Role
The person hired for this opportunity will provide regulatory support to marketed device product teams.

As an Advanced Regulatory Affairs Associate, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:

  • Providing regulatory support and guidance to assigned medical device platform operations teams.
  • Choosing regulatory pathway and provide complete global regulatory assessment of proposed product changes.
  • Coordinating the preparation of US and global regulatory registrations for medical device products.
  • Inputting into requirements for medical product labeling, claims, advertising, and approve final versions.
  • Your Skills and Expertise
    To set you up for success in this role from day one, 3M is looking for candidates who must have the following qualifications:

  • Possess a Bachelors degree or higher (completed and verified prior to start) from an accredited institution
  • Minimum of one (1) yearcombined regulatory affairs and/or medical device experience within a private, public, government or militaryenvironment
  • Additional qualifications that could help you succeed even further in this role include:

  • Possess expertise equivalent to that which would be obtained in masters degree or higher
  • Advanced regulated medical product experience working inregulatory affairs, laboratory and/or quality or other related function
  • Understanding of medical device regulations and/orquality systems
  • Experiencein medical product design and/orsupport
  • Travel: May include up to 5% domestic/international

    Relocation Assistance: Is not authorized

    Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).

    Supporting Your Well-being

    3M offers many programs to help you live your best life both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope.

    Resources for You

    For more details on what happens before, during and after the interview process, check out the Insights for Candidates page at

    Associated topics: blood collection, laboratory, medical, medical laboratory science, microbiology, pathology, scientist, technician ii, technologist, toxicology

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