Symmetrio is recruiting for our client for a Regulatory Affairs Manager to lead U.S. regulatory strategy and submissions for innovative healthcare software products. This role will focus on FDA 510(k) submissions and regulatory pathways for Software as a Medical Device (SaMD) within a global, multinational environment.   
Key Responsibilities 
- Lead preparation and submission of FDA 510(k) filings for healthcare software and digital health products 

- Develop and execute regulatory strategies supporting product development and commercialization 

- Collaborate with product development, quality, clinical, and engineering teams to ensure regulatory compliance 

- Interpret FDA guidance related to medical device software and digital health technologies 

- Partner with global regulatory teams to support international regulatory initiatives 

Requirements
- 5–10+ years of regulatory affairs experience in medical devices or healthcare software 

- Proven experience with FDA 510(k) submissions, ideally for software-based medical devices 

- Strong knowledge of SaMD, FDA regulations, and quality standards (21 CFR Part 820, ISO 13485, IEC 62304) 

- Experience working within a multinational organization 

- Strong cross-functional collaboration and communication skills