Regulatory Affairs Intern — Global Submissions & Mentorship

Stryker; Tempe (AZ); On-site; USD 28,000 - 48,000; Full time

Benefits offered by this job

Hourly wage $20–$35

Sign-on bonus

11 paid holidays annually

Housing stipend or corporate housing

Job summary

Stryker, a global leader in medical technologies, offers an RA internship in Tempe that provides exposure to global regulatory strategy and cross-functional teams including R&D, Supplier Quality, Marketing, and Clinical Affairs. You’ll contribute to regulatory submissions and post-market activities while developing practical skills in a fast-paced environment.

You will shadow RA specialists, support change notifications, and help ensure product registrations reach patients safely.

Qualifications

• Enrolled in BS/MS in a scientific/technical discipline.
• GPA 3.0 or higher (verified at hire).
• Authorized to work in the U.S. without sponsorship.
• Strong communication and collaboration skills.

Responsibilities

• Perform regulatory intelligence activities and monitor global regulations.
• Assist with preparing regulatory submissions to register products internationally.
• Shadow RA Specialists during product development meetings.
• Support post-market regulatory reporting projects to monitor device performance.
• Contribute to regulatory assessments and change notification strategies.

Skills

Strong communication

Leadership

Problem solving

Organizational skills

Microsoft Office proficiency

Education

Bachelor's or Master’s in Mechanical Engineering

Biomedical Engineering

Biology

Chemistry

Tools

Microsoft Office

Job description

Stryker, a global leader in medical technologies, offers an RA internship in Tempe that provides exposure to global regulatory strategy and cross-functional teams including R&D, Supplier Quality, Marketing, and Clinical Affairs. You’ll contribute to regulatory submissions and post-market activities while developing practical skills in a fast-paced environment.

You will shadow RA specialists, support change notifications, and help ensure product registrations reach patients safely.