Regulatory Affairs Intern: Global Submissions (Paid)

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

Benefits offered by this job

Sign-on bonus

11 paid holidays annually

Housing stipend or corporate housing

Job summary

Stryker Group is seeking a Regulatory Affairs intern in the United States. You will gain exposure to global regulatory strategy and work with R&D, Supplier Quality, Marketing, and Clinical Affairs to ensure products meet regulatory requirements.

Ideal candidates are pursuing science-related degrees, have a ≥3.0 GPA, and demonstrate strong communication, leadership, and teamwork. The role offers hands-on regulatory experience and a fast-paced clinical environment.

Qualifications

• Pursuing a Bachelor’s or Master’s degree in a related field with demonstrated academic excellence.
• 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 and ability to collaborate.

Responsibilities

• 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.

Skills

Regulatory knowledge

Communication skills

Leadership

Team collaboration

Problem-solving

Education

Bachelor’s or Master’s degree in Biology, Chemistry, Biomedical Engineering, Healthcare or related field

Tools

Microsoft Office (Excel, Word, PowerPoint)

Job description

Stryker Group is seeking a Regulatory Affairs intern in the United States. You will gain exposure to global regulatory strategy and work with R&D, Supplier Quality, Marketing, and Clinical Affairs to ensure products meet regulatory requirements.

Ideal candidates are pursuing science-related degrees, have a ≥3.0 GPA, and demonstrate strong communication, leadership, and teamwork. The role offers hands-on regulatory experience and a fast-paced clinical environment.