Regulatory Reporting Specialist
Stryker is currently seeking a Regulatory Reporting Specialist to join our Joint Replacement Division to be based hybrid in Weston, FL. As the Regulatory Reporting Specialist, you will be responsible for ensuring the organization's compliance with FDA, European, and global requirements governing adverse event reporting. In this role, you will gain the clinical and regulatory experience required to accurately assess the reportability status of incoming complaints associated with hip, knee, limb salvage, and robotic devices utilizing risk documentation. In addition to managing adverse event reporting activities, you will have the opportunity to collaborate with several post-market teams and support continuous improvement and efficiency projects.
Responsibilities include :
Qualifications : Required :
Preferred :
Health benefits include : Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include : Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance.
Stryker 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.
Regulatory Reporting • Fort Lauderdale, FL, US