[주요업무 내용] Support RAQA team in preparing submission dossiers for new registrations, license amendments, and renewals Assist with license amendments for Class I and II devices as needed Support QMS activities to ensure compliance with MDA, ISO 13485, and Stryker standards Participate in various internal and external RA/QA projects [후보자 필수 자격요건] Demonstrated interest in Regulatory Affairs Familiarity with medical device regulations and relevant terminology Proficiency in English preferred MS Offices 활용 가능자 (PPT, Excel, Word) Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.