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Regulatory Affairs Intern

Regulatory Affairs Intern

Boston ScientificMaple Grove, MN, US
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Regulatory Affairs Intern

At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing whatever your ambitions.

Interns working in Regulatory will support many of our global commercial products by working on regulatory submissions, upholding global regulatory requirements, maintaining internal regulatory file documentation and supporting continuous improvement activities.

Your Responsibilities will include :

  • Learn regulatory requirements to commercialize medical devices
  • Support EU MDR Technical Documentation updates
  • Prepare and submit regulatory submissions (potential example - FDA PMA supplement for a manufacturing change)
  • Use regulatory advocacy to influence the regulatory process
  • Collaborate with cross functional partners to support product and manufacturing changes and draft assessments regarding compliance with applicable regulations

Required Qualifications :

  • Must graduate between Fall 2026 and Spring 2027
  • Currently pursuing a degree in a Science or Healthcare related major, OR Engineering, Exercise Science, Psychology, Math, Business, English or Communications, OR a Master's degree in Regulatory Affairs, Clinical Affairs, or Public Health
  • Must be able to commit to one of the following full internship program periods : May 18th August 7th OR May 26th August 14th
  • Must be eligible to work in the U.S. without company sponsorship, now or in the future, for employment-based work authorization
  • Must have reliable transportation to and from the Maple Grove, MN or Arden Hills, MN Boston Scientific Corporate location
  • Experience with Office Suite : PowerPoint, Word, Excel, Outlook
  • Prior experience with owning and executing a project with a direct output (study or experiment)
  • Preferred Qualifications :

  • Technical writing experience
  • Experience in medical device or healthcare field, in a school or professional environment
  • Must possess excellent written and verbal communication skills
  • Display basic understanding of data collection, analysis and interpretation tools, techniques and outcomes
  • Confident presentation skills preferred
  • Ability to translate technical information into clearly written documents
  • Quick learner, self-motivated, independent worker
  • So, choosing a career with Boston Scientific isn't just business, it's personal. And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

    Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

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    Regulatory Intern • Maple Grove, MN, US