Senior Consultant - MedTech QMS

What you’d do

Lead QMS software implementations for MedTech customers, analyzing business processes and requirements, managing communication between implementation teams and stakeholders, and building adoption roadmaps. Full-time remote role based in Boston, Massachusetts. Found on the employer's careers page on Oct 21, 2026. Apply through the link.

You’ll need

• 6+ years in GMP systems ownership or software consulting
• Knowledge of FDA and EU MDR/IVDR requirements
• Understanding of ISO 13485 and ISO 14971
• Familiarity with 21 CFR Part 803/820/822/806 and EU GMP Annex 11
• QMS implementation experience