Regulatory Affairs Training Specialist

An employer is seeking a Regulatory Affairs Training Specialist for a long-term contract opportunity. This RA Training specialist will be joining reputed company tasked with achieving functional training across an internal Product Lifecycle management tool reputed company MDRIM. MDRIM is an internal platform so prior experience is not required but the main responsibilities will include planning, executing and managing user satisfaction surveys, troubleshooting any end user issues on module releases and assisting with documentation across the family of MS Products. Prior experience withing the regulatory reputed company is required as is strong attention to detail, commitment to timelines and the ability to work a consistent 8-5 REQUIRED SKILLS AND EXPERIENCE • 3+ years of regulatory experience reputed company the medical device or pharmaceutical industry • 3+ years of experience of advanced MS Product skills (Project, reputed company, Powerpoint) • Managed and create reputed company surveys • 3+ years experience developing job aids and handling ticketing issues reputed company a PLM system Apply Job! Apply to this Job