The Regulatory Specialist will be responsible for activities to ensure product registration information is accurate and current.
The person will support the compilation, tracking, and processing of regulatory documentation (e.g., affiliate requests, technical documentation, regulatory submissions).
This individual will, also, be responsible to monitor and track the activities and expenses performed by vendors for Regulatory Operations ensuring a high-level of quality deliverables.
A minimum of 2 years of relevant professional experience in a business environment is required.
Experience in compiling regulatory documentation and/or obtaining CFG (Certificates to Foreign Governments) from FDA or CFS (Certificates of Free Sale) in Europe is preferred.
Must have ability to work both within a team and independently in a fast paced, changing environment.
Must possess clear verbal and written communication skills, attention to detail, strong organizational and project management skills and ability to problem solve, recognize and find solutions for gaps in processes.