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Senior Consultant - MedTech QMS Complaints

Minnesota - Minneapolis🌐 Remote💼 Full-time💰 $80,000–$80,000🗓 2025-06-23 → 2026-09-26

Core

Lead MedTech Complaints implementations and guide the transformation of customers' Complaints Management processes and technology for Veeva's Quality Management solutions.

Role type

Senior MedTech Quality Management Consultant (Complaints)

Builds

QMS implementations and customer adoption roadmaps for Vault

Domain

Life Sciences / MedTech / Quality Management Systems

Deliverable

production ML models | product features | dashboards & analysis | client delivery

Required skills

GMP Systems ownership, Complaints Management (Medical Device), FDA/EU MDR/IVDR regulatory knowledge, CAPA/Risk Management process understanding, ISO 13485/14971 compliance, SaaS/GxP principles, Data/Content Management applications

Preferred skills

Veeva Vault implementation, Management Consulting, Change Management, Field Action/Product Return, Clinical Medical Device/Biologics/SaMD

Technologies

Vault

Responsibilities

Review and analyze customer business processes to identify gaps and requirements, Lead QMS Complaints implementation workstreams, Function as primary customer liaison, Develop customer adoption and enhancement roadmaps, Guide customers in adopting Vault and industry best practices

Seniority

Senior, hands-on IC

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