
Senior Consultant - MedTech Regulatory Implementation
Veeva is hiring a Senior Consultant to lead MedTech RIM implementations globally, guiding Regulatory Affairs and Operations transformations and ensuring customer adoption. Requires 8+ years in systems implementation, GxP ownership, or software consulting and 4+ years in Regulatory Affairs/Operations within Medical Device or Diagnostics. Experience with Veeva RIM or similar RIM solutions and knowledge of FDA, EU MDR/IVDR, UDI, and technical documentation is required. Location listed as Philadelphia, PA; role advertised as Work Anywhere/remote eligible. Base salary range: $80,000–$200,000 USD per year.









