Summary

This mid-level Quality Operations Program Manager role owns document control and quality management processes across regulated life sciences products and systems. The role is remote and focuses on regulatory oversight, validation, quality records, process effectiveness, and compliance within Veeva's QMS.

Responsibilities

• Own document control processes and quality records
• Oversee regulated activities and product deliverables
• Define and maintain quality management processes
• Interpret regulations and guide quality requirements
• Develop metrics for system effectiveness
• Support validation testing and product changes