Summer 2025 Intern - Medical Writer - Virginia

Work Flexibility: Onsite

Are you passionate about positively impacting worldwide access to medical devices? Stryker Spine is seeking a motivated Medical Affairs and Post-Market Surveillance Intern to join our team! This internship offers a comprehensive experience, exposing you to new product development (NPD), post-market clinical follow-up (PMCF), and post market surveillance (PMS) reporting! You will gain valuable insights into global medical device regulations and guidance documents as they pertain to post-market reporting requirements, clinical safety and performance, designing and executing systematic literature searches, compiling, analyzing, and benchmarking key safety and performance outcomes, and pre-and post-market safety and performance considerations for NPDs.

Who we want​

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Challengers. People who seek out the hard projects and work to find just the right solutions.​

Teammates. Partners who listen to ideas, share thoughts and work together to move the business forward.​

Charismatic networkers. Relationship-savvy people who intentionally make connections with both internal partners and external contacts.​

Strategic thinkers. Interns who propose innovative ideas and consistently exceed their performance objectives.​

Customer-oriented achievers. Individuals with an unparalleled work ethic and customer-focused attitude who bring value to their partnerships.​

Game changers. Persistent interns who will stop at nothing to live out Stryker’s mission to make healthcare better. ​

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What You Get Out of the Internship​​

Stryker, a global leader in medical technology takes great pride in their people, and that’s why we’re looking to expand our talent. As a result, we are looking for the best and brightest students to strengthen our team and drive our business going forward. As a Regulatory intern at Stryker, you will:​

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• 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​

• Learn about regulations within the medical device industry​​

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What You Need​​

• Currently working on completion of a Bachelor’s or Master’s degree in related field or equivalent; we will only consider students who plan to be enrolled in a degree-seeking program after the summer.​

• Cumulative 3.0 GPA or above; must be the case at the date of hire and will be verified during background check in the spring​

• Must be legally authorized to work in the U.S. and not require employment-based sponsorship now or in the future.​

• Excellent written and verbal communication skills. ​

• Strong interpersonal skills.​

• Ability to exercise independent judgment and proven leadership and business acumen skills. ​

• Proven ability to handle multiple projects and meet deadlines. ​

• Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm.