
Senior Consultant - MedTech QMS Complaints
Experienced consultant role to lead Complaints Management implementation workstreams for Veeva’s MedTech QMS customers. Responsibilities include analyzing customer processes, leading implementations, acting as primary customer liaison, and guiding post-implementation adoption. Requirements include 8+ years in GMP systems ownership or software consulting and 5+ years in medical device complaints management, with strong knowledge of FDA and EU regulations and standards (ISO 13485, ISO 14971).