Freelance SaMD Quality & Regulatory Lead

A technology solution provider is seeking a Quality & Regulatory Affairs Manager for a 3-month freelance engagement in the United States. This role focuses on the retroactive normalization and completion of technical documentation related to SaMD. The ideal candidate will have strong experience with MedTech documentation, knowledge of ISO 13485 and FDA requirements, and proven skills in organizing compliance documentation. This position requires a hands-on mindset, English proficiency, and commitment for the project duration. #J-18808-Ljbffr