MedTech Regulatory Implementation Lead - Remote

Veeva Systems, Inc.; Illinois; Hybrid; USD 80,000 - 200,000; Full time

Benefits offered by this job

Medical, dental, vision, and basiclife

Flexible PTO and holidays

Retirement programs

1% charitable giving program

Job summary

Veeva Systems, Inc. is seeking an experienced MedTech Regulatory Information Management consultant to lead implementations worldwide. You will guide Regulatory Affairs and Operations transformations, working with Professional Services to deliver end-to-end data and documentation workstreams.

The role emphasizes cross-team collaboration, customer liaison, and building adoption roadmaps while applying industry standards such as FDA, EU MDR/IVDR, and UDI.

Qualifications

• 8+ years in systems implementation or software consulting.
• 4+ years in Regulatory Operations in MedTech/Diagnostics.
• Direct experience implementing Veeva RIM or similar.
• Strong understanding of FDA, EU MDR/IVDR, and UDI.
• Excellent verbal and written communication.

Responsibilities

• Lead RIM implementation workstreams for MedTech Regulatory solutions.
• Review and analyze existing customer processes to identify gaps.
• Function as primary customer liaison among teams and stakeholders.
• Analyze customer requirements and new product features for adoption roadmaps.
• Guide customers in adopting Veeva RIM and best practices.

Skills

Systems implementation

Regulatory operations

Veeva RIM

Global regulatory knowledge

IT project leadership

Communication skills

Job description

Veeva Systems, Inc. is seeking an experienced MedTech Regulatory Information Management consultant to lead implementations worldwide. You will guide Regulatory Affairs and Operations transformations, working with Professional Services to deliver end-to-end data and documentation workstreams.

The role emphasizes cross-team collaboration, customer liaison, and building adoption roadmaps while applying industry standards such as FDA, EU MDR/IVDR, and UDI.