At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised. **What You Can Expect** Under supervision of the Clinical Project Manager, the Clinical Affairs Intern (CAI) is responsible for administrative activities in support of ongoing MDR and Clinical projects supporting the hip, knees, sport medicine, trauma and extremities businesses. This position requires basic knowledge and understanding of medical device industry, regulatory, product lifecycle data, and project management concepts. May perform some or all of the following functions, depending upon their specific assigned focus. **How You'll Create Impact** + Collaborating with multiple stakeholders to establish objectives, timelines and milestones in Medical Writing and Post Market Surveillance (PMS) Department + Participating in project teams (meetings, presentations, etc.) + Supports the team members in proper tracking of project activities + Reporting out to Leadership on the status of projects, issues and mitigations + Optimize product lifecycle traceability **What Makes You Stand Out** + Basic computer skills, including Microsoft Office Suite + Strong writing and communication skills + Strong interpersonal skills + Strong Analytical Skills with affinity for details + Versatility, flexibility, and willingness to work with changing priorities + Strong organizational, teamwork, problem-solving and analytical skills are essential + Ability to work autonomously and efficiently on specific tasks + Ability to work with rapid changes + Ability to learn regulations pertinent to medical devices + Ability to learn basics of medical device regulations + Ability to handle multiple projects and meet deadlines, working closely with RA Specialists and Managers **Your Background** + Must be actively enrolled in an academic program for the entire duration of the assignment + Must be available to work full-time (40 hours/week) throughout the co-op session + Must be authorized to work in the U.S. without requiring employer sponsorship + Pursuing a Bachelor's degree in health, life sciences, or engineering disciplines + A minimum GPA of 3.0 is strongly preferred **Travel Expectations** + Up to 5% EOE/M/F/Vet/Disability