2026 Summer Intern Regulatory Affairs California

StrykerSan Jose, CA
127d$19 - $34

About The Position

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. You will network with key/high-level stakeholders and leaders of the business, be a part of an innovative team and culture, and experience documenting complex processes and presenting them in a clear format.

Requirements

  • 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.

Nice To Haves

  • Majors in scientific or technical disciplines preferred (e.g., Biomedical Engineering, Biological Sciences, Chemistry, or related fields).

Responsibilities

  • Perform regulatory intelligence activities to monitor changes in global regulations and support strategy updates.
  • Assist with preparing regulatory submissions to register products internationally.
  • Shadow RA Specialists during new product development meetings to gain insight into the collaborative design and development process.
  • Support post-market regulatory reporting projects that help monitor device performance and identify potential safety or quality issues.
  • Contribute to the development of regulatory assessments and change notification strategies to minimize disruption to product registrations or approvals.

Benefits

  • $19.50 min hourly wage - $34.50 max hourly wage.
  • Sign-on bonus.
  • Paid holidays.
  • Paid corporate housing or a living stipend, dependent upon hiring location.

Stand Out From the Crowd

Upload your resume and get instant feedback on how well it matches this job.

Upload and Match Resume

What This Job Offers

Job Type

Full-time

Career Level

Intern

Industry

Miscellaneous Manufacturing

Education Level

Bachelor's degree

© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service