Regulatory Affairs Specialist II

Regulatory Affairs Specialist II - (RAS
2.1) Company Description

Stereotaxis is the global leader in innovative robotic technologies designed to enhance the treatment of arrhythmias and perform endovascular procedures. Its mission is the discovery, development and delivery of robotic systems, instruments, and information solutions for the interventional laboratory. These innovations help physicians provide unsurpassed patient care with robotic precision and safety, improved lab efficiency and productivity, and enhanced integration of procedural information.

Core components of Stereotaxis’ systems have received regulatory clearance in the United States, European Union, China, Japan, Canada, and elsewhere. For more information, please visit

The Regulatory Affairs Specialist II provides hands‑on regulatory affairs support for new product marketing approvals and renewals for existing products, including development of regulatory requirements/strategies and preparation of submissions. This individual will represent Stereotaxis Regulatory with international regulators on submission reviews/approvals and ensure compliance with required regulations and established corporate standards.

• Evaluates potential global regulatory pathways for US, EU, and international product launches/enhancements as an active member of Product Development team(s).
• Prepares global regulatory submissions to regulatory authorities, including the FDA, EU Notified Bodies, and other regulatory authorities.
• Interacts directly with regulatory agencies on products/projects at reviewer level.
• Provides regulatory guidance to assigned product development teams to ensure the documents the team develops will meet the needs of regulatory submissions.
• Reviews technical documentation, such as test reports and test protocols, for completeness and compliance with regulatory standards, using scientific judgment to guide the teams in understanding how to close any gaps that exist.
• Timely compiles materials for license renewals, updates, and registrations.
• Reviews company marketing literature for compliance with applicable regulations.
• Maintains a thorough knowledge of current QSR and ISO requirements as they apply.

• B.S. Degree in a Science or Engineering field highly preferred and/or business experience.
• 3‑5 years’ experience in regulated medical device industry highly preferred.
• Knowledge of global Class I, II and/or III hardware/software/sterile medical device requirements.
• Extensive knowledge of global quality system requirements preferred.
• RAC Certification preferred.
• Ability to communicate effectively required.
• Ability to interpret domestic and international regulations as they apply to company activities.
• Demonstrated project management skills to plan, conduct and implement system assessments.
• Legally authorized to work in the United States.

This role is an in‑office position at our Rogers, MN facility.