Position Summary: 

The incumbent will manage the regulatory process, both domestic and international markets, for  NxStage Medical, Inc. products and provide regulatory input into key quality system processes, such as design controls, change control, labeling and advertising, and others.  

Responsibilities: 

• Develop regulatory strategies and plans for NxStage Medical, Inc. products. 

• Prepare and submit US regulatory submissions including 510(k)’s, IDE’s, etc.  

• Prepare and submit international regulatory submissions, as international market develops.  This includes but is not limited to Canada, Europe (CE Mark), Mexico, Asia, etc.  

• Communicate directly with senior management, economic operators, and regulatory agencies on all regulatory issues.  

• Monitor regulations, guidance and standards and communicate applicable requirements to affected departments of NxStage. 

• Determine impact of product and system changes on regulatory status for both US and OUS distributions. 

• Prepare documentation to support no-filing decisions for US & International Markets.  

• Participate on cross-functional developmental teams including project planning and design review activities.  

• Participate in compliance related activities, including Quality System Audits, labeling reviews, and verification/validation reviews. 

• Maintain corporate regulatory files. 

Education & Qualifications: 

• B.S. in technical discipline preferred or equivalent experience 

• 8+ years’ experience in domestic and international Regulatory Affairs in the medical device industry  

• Experience interacting with FDA regarding regulatory matters  

• Expertise in working within Medical Device Regulations including Quality System Regulation 21 CFR Part 820, ISO 13485, EU MDD/MDR, Canadian Regulations 

• Experience in product development of medical devices a plus