Regulatory specialist

• 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.

• Must be proficient with MS Office applications.

Regards,

Indu Dubey
Clinical Recruiter
732-844-8725 

indu @irionline.com