Job Description

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 it’s 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 other curious, creative 3Mers.

This position provides an opportunity to transition from other private, public, government or military experience to a 3M career.

The Impact You’ll Make in this Role

As a 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:

Lead/coordinate regulatory operations systems and master data support; organizational subject matter expert
Lead connection with IT to represent regulatory needs for systems as required; represent design requirements for system
Provide support and expertise as part of the Regulatory organization using knowledge of Global regulatory systems requirements and paths to support achievement of business objectives.
Prepare Technical and Regulatory documentation for Consumer Health products
Own and update regulatory master data as required
Assure that device listings, import licenses, establishment licenses, and registrations for Consumer Health products are accurate and up to date 
Advise on new regulatory requirements impacting systems and regulatory operations

Your Skills and Expertise 

To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications:

Bachelor’s degree or higher (completed and verified prior to start)
Three (3) years of combined experience in Regulatory Affairs, Quality Systems, or regulated R&D in a private, public, government or military environment

Additional qualifications that could help you succeed even further in this role include:

Master's degree in from an accredited institution
Medical Device Regulatory Affairs experience with FDA
EU MDR experience
Regulatory operations experience and process/systems understanding
International regulatory experience
Consumer experience
IT, master data, or system experience (e.g. SAP, data syndication tools, agency databases, etc.)
Ability to interface with regulatory agencies and support audits
Proficient in Microsoft Office Tools

Work location:

Hybrid Eligible (Job Duties allow for some remote work but require travel to Maplewood)

Travel: May include up to 5% domestic/international

Relocation Assistance: May be 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. 

Chat with Max

For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting assistant on 3M.com/careers.