Summer 2027 RA/QA Internship

What You Get Out of the Internship

At Stryker, developing the next generation of talent is 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 shaping the future of healthcare.

• Apply classroom knowledge and gain experience in a fast-paced, growing industry.
• Implement new ideas, be constantly challenged, and develop your skills.
• Network with key/high-level stakeholders and business leaders.
• Be part of an innovative team and culture.
• Experience documenting complex processes and presenting them clearly.

Who We Want

Challengers: People who seek out hard projects and work to find the right solutions.

Teammates: Partners who listen to ideas, share thoughts, and work together to move the business forward.

Charismatic networkers: Relationship-savvy people who intentionally connect with internal partners and external contacts.

Strategic thinkers: Interns who propose innovative ideas and consistently exceed performance objectives.

Customer-oriented achievers: Individuals with an unparalleled work ethic and customer-focused attitude who bring value to partnerships.

Game changers: Persistent interns who will stop at nothing to live out Stryker's mission to make healthcare better.

Opportunities Available

As a Regulatory Affairs (RA) intern at Stryker, you will gain exposure to global regulatory strategy and compliance while working cross-functionally with teams such as R&D, Supplier Quality, Marketing, and Clinical Affairs. You will contribute to projects that ensure our products meet regulatory requirements and reach patients safely and effectively.

• 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.

What You Need

• Currently pursuing a Bachelor's or Master's degree in a scientific or technical discipline (e.g., Biomedical Engineering, Biological Sciences, Chemistry, Software Engineering, or related fields) and 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.

Compensation: $20 min hourly wage to $35 max hourly wage, sign-on bonus, 11 paid holidays annually, and either paid corporate housing or a living stipend, dependent upon hiring location.