Regulatory Affairs Intern: Mentorship & Global Impact

Stryker; Portage (MI); On-site; USD 28,000 - 48,000; Full time

Benefits offered by this job

Sign-on bonus

Housing stipend

Paid holidays

Job summary

Stryker in Portage, MI offers a Regulatory Affairs internship where you contribute to meaningful projects, gain leadership mentorship, and join an innovative team shaping healthcare. You’ll work with RA peers and cross-functional partners to ensure products meet regulatory requirements and reach patients safely.

You will participate in regulatory submissions, post-market monitoring, and strategy discussions, while developing critical analytics and presentation skills.

Qualifications

• 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.

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.

Education

Bachelor's or Master’s degree

Job description

Stryker in Portage, MI offers a Regulatory Affairs internship where you contribute to meaningful projects, gain leadership mentorship, and join an innovative team shaping healthcare. You’ll work with RA peers and cross-functional partners to ensure products meet regulatory requirements and reach patients safely.

You will participate in regulatory submissions, post-market monitoring, and strategy discussions, while developing critical analytics and presentation skills.