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 a team tasked with achieving functional training across an internal Product Lifecycle management tool called 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 space 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 within the medical device or pharmaceutical industry
- 3+ years of experience of advanced MS Product skills (Project, Outlook, Powerpoint)
- Managed and create customer success surveys
- 3+ years experience developing job aids and handling ticketing issues within a PLM system
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