Regulatory Affairs Intern: Global Submissions & Strategy

Stryker

Portage (MI)

On-site

USD 28,000 - 48,000

Full time

14 days+

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

Sign-on bonus
11 paid holidays annually
Housing stipend

Job summary

Stryker is seeking a Regulatory Affairs intern to gain hands-on experience with global regulatory strategy and compliance while working cross-functionally with R&D, Supplier Quality, Marketing, and Clinical Affairs.

You will contribute to regulatory submissions, shadow specialists, and support post-market reporting. Applicants should be pursuing a Bachelor's or Master’s in a related field with a 3.0+ GPA and U.S. work authorization.

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

  • 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

Communication
Leadership
Problem-solving
Organizational skills
Collaboration

Education

Bachelor's or Master's degree in related field

Tools

Microsoft Office

Job description

Stryker is seeking a Regulatory Affairs intern to gain hands-on experience with global regulatory strategy and compliance while working cross-functionally with R&D, Supplier Quality, Marketing, and Clinical Affairs.

You will contribute to regulatory submissions, shadow specialists, and support post-market reporting. Applicants should be pursuing a Bachelor's or Master’s in a related field with a 3.0+ GPA and U.S. work authorization.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Remote Regulatory Affairs Intern: Post‑Market Submissions
Remote Regulatory Affairs Intern: Post‑Market Submissions

Stryker • Florida

Hybrid
USD 28,000 - 48,000
Summer 2027 Internship RAQA Regulatory Affairs Michigan
Summer 2027 Internship RAQA Regulatory Affairs Michigan

Stryker • Portage (MI)

On-site
USD 28,000 - 48,000
Sign-on bonus
11 paid holidays annually
Housing stipend
Global Regulatory Affairs Specialist (Hybrid)
Global Regulatory Affairs Specialist (Hybrid)

Stryker • Irvine (CA)

Hybrid
USD 110,000 - 183,000
Senior Regulatory Affairs Leader - M&A & Lifecycle Strategy
Senior Regulatory Affairs Leader - M&A & Lifecycle Strategy

Regulatory Toolkit • Portage (MI)

Hybrid
USD 127,000 - 211,000
Hybrid work arrangement
Onsite Clinical Affairs Internship: Cross-Functional Impact
Onsite Clinical Affairs Internship: Cross-Functional Impact

Stryker • Portage (MI)

On-site
USD 28,000 - 48,000
Sign-on bonus
11 paid holidays annually
Corporate housing or living stipend
Staff International Regulatory Affairs Specialist
Staff International Regulatory Affairs Specialist

Regulatory Toolkit • Irvine (CA)

Hybrid
USD 110,000 - 183,000
Remote QA Intern: Drive Healthcare Quality
Remote QA Intern: Drive Healthcare Quality

Stryker Employment Company, LLC • Flower Mound (TX)

Remote
USD 28,000 - 48,000
Sign-on bonus
11 paid holidays annually
Housing stipend or corporate housing
Senior Regulatory Affairs Specialist - Medical Devices
Senior Regulatory Affairs Specialist - Medical Devices

Regulatory Toolkit • Redmond (WA)

Hybrid
USD 96,000 - 160,000
Biomedical R&D Lab Analyst Intern
Biomedical R&D Lab Analyst Intern

Stryker • Tennessee

Hybrid
USD 28,000 - 48,000
Sign-on bonus
11 paid holidays annually
Housing stipend or corporate housing
Remote Regulatory Affairs Lead, Medical Devices
Remote Regulatory Affairs Lead, Medical Devices

Regulatory Toolkit • United States

Remote
USD 110,000 - 190,000