Regulatory Affairs Intern - Global Submissions & Strategy

Stryker; Fremont (CA); On-site; USD 28,000 - 48,000; Full time

Benefits offered by this job

Sign-on bonus

11 paid holidays annually

Housing stipend or corporate housing

Job summary

Stryker is seeking a Regulatory Affairs intern in California to gain exposure to global regulatory strategy and compliance while collaborating with R&D, Supplier Quality, Marketing, and Clinical Affairs. You will contribute to projects ensuring products meet regulatory requirements and reach patients safely and effectively.

Ideal candidates are pursuing a Bachelor’s or Master’s in a related field, with a 3.0+ GPA, and legal work authorization in the U.S.

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.
• Proficiency in Microsoft Office (Excel, Word, PowerPoint) and eagerness to learn in a dynamic environment.

Responsibilities

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

Skills

Strong communication

Leadership

Problem solving

Organizational skills

Microsoft Office

Education

Bachelor’s or Master’s degree in a related field

Tools

Microsoft Office

Job description

Stryker is seeking a Regulatory Affairs intern in California to gain exposure to global regulatory strategy and compliance while collaborating with R&D, Supplier Quality, Marketing, and Clinical Affairs. You will contribute to projects ensuring products meet regulatory requirements and reach patients safely and effectively.

Ideal candidates are pursuing a Bachelor’s or Master’s in a related field, with a 3.0+ GPA, and legal work authorization in the U.S.