Job Description
Stryker is currently seeking a **Staff Regulatory Affairs Specialist** to join our **Ortho Tech – Mako and Enabling Technologies** division to be based in **Weston, Florida** or **remotely** anywhere within the United States.
As the **Staff Regulatory Affairs Specialist** , you will join a regulatory affairs team supporting a portfolio of advanced orthopedic technologies across U.S. and global markets. You will work cross-functionally to ensure products remain compliant and available in dynamic regulatory environments. This role focuses on sustaining regulatory compliance, managing post-market activities, and supporting submission strategies for modified and existing products.
**What you will do**
+ Develop and execute regulatory strategies for post-market products to maintain market access across global regions.
+ Evaluate regulatory requirements and identify submission pathways for product changes, ensuring alignment with applicable regulations....
As the **Staff Regulatory Affairs Specialist** , you will join a regulatory affairs team supporting a portfolio of advanced orthopedic technologies across U.S. and global markets. You will work cross-functionally to ensure products remain compliant and available in dynamic regulatory environments. This role focuses on sustaining regulatory compliance, managing post-market activities, and supporting submission strategies for modified and existing products.
**What you will do**
+ Develop and execute regulatory strategies for post-market products to maintain market access across global regions.
+ Evaluate regulatory requirements and identify submission pathways for product changes, ensuring alignment with applicable regulations....