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 Manage scope traceability for files under MDR regulationsCollaborating with multiple stakeholders to establish objectives, timelines and milestones in Medical Writing and Post Market Surveillance (PMS) DepartmentParticipating in project teams (meetings, presentations, etc.)Supports the team members in proper tracking of project activitiesReporting out to Leadership on the status of projects, issues and mitigationsWhat Makes You Stand Out Basic computer skills, including Microsoft Office SuiteStrong writing and communication skillsStrong interpersonal skillsStrong Analytical Skills with affinity for detailsVersatility, flexibility, and willingness to work with changing prioritiesStrong organizational, teamwork, problem-solving and analytical skills are essentialAbility to work autonomously and efficiently on specific tasksAbility to work with rapid changesAbility to learn regulations pertinent to medical devicesAbility to learn basics of medical device regulationsAbility to handle multiple projects and meet deadlines, working closely with RA Specialists and ManagersYour Background Must be actively enrolled an academic program for the entire duration of the assignment.Pursuit of Bachelor’s Degree in the health, life sciences, or engineering disciplines.GPA of 3.0 or higher is strongly preferredTravel Expectations Up to 5%EOE/M/F/Vet/Disability