Demo

Validation Consultant Lead

i-Pharm Consulting
Bedford, MA Full Time
POSTED ON 4/22/2025
AVAILABLE BEFORE 5/20/2025

Main Responsibilities

  • Provide execution and oversight across CQV projects, ensuring protocols, tests, and activities are properly planned and executed with minimal guidance.
  • Lead by example, mentor team members, and drive best practices in equipment validation.
  • Identify the right CQV approaches needed based on industry best practices.
  • Promote a deadline-driven and accountable work environment, identifying issues early and driving them to resolution.

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