
Senior Consultant - MedTech QMS Complaints
Experienced consultant role focused on leading Complaints Management implementations for MedTech customers using Veeva's QMS solutions. Requires experience analyzing customer processes, leading implementation workstreams, liaising with stakeholders, and guiding post-implementation adoption. Requires 8+ years in GMP systems ownership or software consulting and 5+ years in medical device complaints management; strong knowledge of FDA and EU regulations and ISO standards. Veeva Vault experience is desirable. Location: Boston, Massachusetts / Remote US.