Stryker-posted 1 day ago
Intern
Onsite • Bloomington, MN
5,001-10,000 employees

At Stryker, we believe that developing the next generation of talent is just as important as developing life-changing medical technologies. As an intern, you won’t just observe — you’ll contribute to meaningful projects, gain exposure to leaders who will mentor you, and experience a culture of innovation and teamwork that is shaping the future of healthcare. As an intern, you will : Apply classroom knowledge and gain experience in a fast-paced and growing industry setting Implement new ideas , be constantly challenged, and develop your skills Network with key/high-level stakeholders and leaders of the business Be a part of an innovative team and culture Experience documenting complex processes and presenting them in a clear format

  • As a Regulatory Affairs Intern, you will gain exposure to regulatory and legal frameworks, requirements, and processes that guide medical device development and compliance.
  • support activities such as gathering and maintaining regulatory data
  • assisting in the preparation of submission documentation
  • contributing to process improvements for key regulatory procedures.
  • Currently pursuing a Bachelor’s or Master’s degree in a related field; must remain enrolled in a degree-seeking program after the internship .
  • Cumulative 3.0 GPA or above (verified at time of hire)
  • Must be legally authorized to work in the U.S. and not require sponsorship now or in the future .
  • Strong written and verbal communication skills, with proven ability to collaborate and build relationships
  • Demonstrated leadership, problem-solving, and organizational skills with the ability to manage multiple priorities
  • Proficiency in Microsoft Office (Excel, Word, PowerPoint) and eagerness to learn in a dynamic environment .
  • Scientific or technical disciplines preferred (e.g., Biomedical Engineering, Biological Sciences, Chemistry, or related fields)
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