Remote MedTech QMS Lead Consultant

Veeva; Minneapolis (MN); Remote; USD 80,000 - 200,000; Full time

Benefits offered by this job

Medical, dental, vision

Flexible PTO

Retirement programs

Charitable giving program

Job summary

Veeva Systems is seeking an experienced MedTech Complaints consultant to lead global QMS implementations. You will guide transformation of customers’ Complaints Management processes and technology, working with Professional Services to ensure delivery success.

The role requires deep GMP/GxP knowledge, FDA/EU MDR experience, and strong communication skills to partner with customers and internal teams across regions.

Qualifications

• 8+ years of GMP systems ownership or software consulting experience.
• 5+ years in Complaints Management for Medical Device products.
• Strong knowledge of FDA/EU MDR/IVDR requirements and reporting.

Responsibilities

• Lead QMS Complaints implementation workstreams for MedTech customers.
• Act as primary liaison between implementation teams and customer stakeholders.
• Analyze requirements and guide adoption of Vault with best practices.

Skills

GMP Systems ownership

Complaints Management

FDA/EU MDR knowledge

SaaS and GxP understanding

Change Management

Stakeholder communication

Consulting

Life Sciences domain knowledge

Data or Content Management

Veeva Vault experience

Tools

Veeva Vault

Job description

Veeva Systems is seeking an experienced MedTech Complaints consultant to lead global QMS implementations. You will guide transformation of customers’ Complaints Management processes and technology, working with Professional Services to ensure delivery success.

The role requires deep GMP/GxP knowledge, FDA/EU MDR experience, and strong communication skills to partner with customers and internal teams across regions.