
Senior Consultant - MedTech Regulatory Implementation
Experienced consultant role to lead RIM implementation workstreams for Veeva’s MedTech customers globally. Responsibilities include analyzing customer processes, configuring systems, serving as primary customer liaison, developing adoption/enhancement roadmaps, and guiding best practices for regulatory data and document management. Requires 8+ years in systems implementation/GxP/software consulting and 4+ years in Regulatory Operations/Regulatory Affairs within Medical Device or Diagnostics; direct experience with Veeva RIM or similar solutions and strong knowledge of global regulatory requirements (FDA, EU MDR/IVDR, UDI). Role is based in Chicago (Work Anywhere policy) and the listed base salary range is $80,000–$200,000 per year.