Regulatory Affairs Specialist

Regulatory Affairs Specialist

This position is responsible for preparing submissions to various regulatory agencies. Additionally, the position will help maintain and improve upon domestic and international compliance. Candidate must possess the ability to work well in a team environment and demonstrate great attention to detail.

This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties may be assigned.

• Prepare and submit regulatory documentation, such as FDA 510(k) premarket notifications, to regulatory agencies, including FDA, Notified Bodies, and Authorized Representatives.
• Prepare, maintain, and submit, when necessary, European Medical Device Directive and European Medical Device Regulation compliant Technical Files.
• Create and/or modify regulatory procedures to remain in compliance with FDA, ISO, European, Canadian, and other standards.
• Work with the international department on various regulatory filings for product registration in different countries.
• Provides regulatory support for other projects as required.
• Updating appropriate personnel on new and revised processes and procedures.

Process, execute, organize and archive various internal documentation related to Engineering and/or Quality Systems.

Preparing change order documentation and routing it for final approval.

Minimum of 2 year college degree, Bachelor's Degree (or greater) preferred. Relevant work experience, preferably in the medical or legal field and/or other regulated industry. Previous experience creating and revising labels and DFUs preferred. Knowledge of European, ISO 13485 and FDA regulations preferred. Knowledge of international regulatory guidelines regarding GMP requirements is desirable.