Job Description
Join Stryker's **Ortho Tech** Division as a **Regulatory Affairs Specialist** and support regulatory activities for products used across a broad portfolio of Orthopedic Instruments. In this role, you will help maintain regulatory compliance, support submission activities, and provide regulatory intelligence that enables products to meet global market requirements. This is an excellent opportunity for an early-career professional to develop foundational regulatory affairs expertise while partnering with cross-functional teams in a highly regulated environment.
**What You Will Do**
+ Monitor regulatory requirements, guidance documents, and industry standards across applicable global markets.
+ Research and compile regulatory requirements, approval pathways, and compliance information for products and programs.
+ Collect, organize, and maintain regulatory intelligence files, submission documentation, and supporting records.
+ Assist in preparing regulatory d...
**What You Will Do**
+ Monitor regulatory requirements, guidance documents, and industry standards across applicable global markets.
+ Research and compile regulatory requirements, approval pathways, and compliance information for products and programs.
+ Collect, organize, and maintain regulatory intelligence files, submission documentation, and supporting records.
+ Assist in preparing regulatory d...
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