Regulatory Affairs Intern: Global Submissions & Strategy

Regulatory Jobs; Tempe (AZ); In loco; USD 28.000 - 48.000; Tempo pieno

Descrizione del lavoro

Stryker invites motivated interns to contribute to meaningful projects in regulatory affairs. You will gain exposure to global regulatory strategy and work with R&D, Supplier Quality, Marketing and Clinical Affairs.

You’ll help ensure products meet regulatory requirements and reach patients safely. Responsibilities include regulatory intelligence, assisting with submissions, shadowing RA Specialists, supporting post-market reporting, and helping develop regulatory assessments and change

Competenze

• Pursuing Bachelor's or Master's degree; must remain enrolled after internship.
• GPA 3.0+ verified at time of hire.
• U.S. work authorization and no future sponsorship required.
• Strong written and verbal communication; collaboration skills.
• Leadership and ability to manage multiple priorities.
• Proficiency in Microsoft Office; eager to learn in a dynamic environment.

Mansioni

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

Conoscenze

Written and verbal communication

Leadership

Problem-solving

Organizational skills

Formazione

Bachelor's or Master's degree in related field

Strumenti

Microsoft Office

Descrizione del lavoro

Stryker invites motivated interns to contribute to meaningful projects in regulatory affairs. You will gain exposure to global regulatory strategy and work with R&D, Supplier Quality, Marketing and Clinical Affairs.

You’ll help ensure products meet regulatory requirements and reach patients safely. Responsibilities include regulatory intelligence, assisting with submissions, shadowing RA Specialists, supporting post-market reporting, and helping develop regulatory assessments and change