RA/QA Intern: Post‑Market Regulatory Strategy

Regulatory Jobs; Town of Florida (NY); Hybrid; USD 28,000 - 48,000; Full time

Benefits offered by this job

Sign-on bonus

11 paid holidays annually

Housing stipend

Job summary

Stryker is seeking a Regulatory Affairs intern in the United States to contribute to global regulatory strategy and compliance while working with R&D, Supplier Quality, Marketing, and Clinical Affairs. You will perform regulatory intelligence, help prepare submissions, and shadow specialists as you gain insight into product development and lifecycle management.

This internship emphasizes collaboration, documentation of complex processes, and presenting findings clearly.

Qualifications

• Pursuing a Bachelor’s or Master’s in a science/technical field and must stay enrolled.
• GPA 3.0+ verified at hire.
• Authorized to work in the U.S. without sponsorship now or in the future.
• Strong written and verbal communication; collaborative mindset.
• Demonstrated leadership, problem solving, and ability to handle multiple priorities.
• Proficiency with Microsoft Office and eagerness to learn in a dynamic environment.

Responsibilities

• Perform regulatory intelligence to monitor global regulation changes and support strategy updates.
• Assist with preparing regulatory submissions to register products internationally.
• Shadow RA Specialists during new product development meetings to learn collaborative design processes.
• Support post-market regulatory reporting to monitor device performance and safety or quality issues.
• Develop regulatory assessments and change notification strategies to minimize disruption to registrations or approvals.

Skills

Regulatory knowledge

Communication

Leadership

Organizational skills

Microsoft Office

Education

Bachelor’s or Master’s degree in a scientific/technical field

Tools

Excel

Word

PowerPoint

Job description

Stryker is seeking a Regulatory Affairs intern in the United States to contribute to global regulatory strategy and compliance while working with R&D, Supplier Quality, Marketing, and Clinical Affairs. You will perform regulatory intelligence, help prepare submissions, and shadow specialists as you gain insight into product development and lifecycle management.

This internship emphasizes collaboration, documentation of complex processes, and presenting findings clearly.