Lead CQV Consultant Job at i-Pharm Consulting, Bedford, MA

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  • i-Pharm Consulting
  • Bedford, MA

Job Description

I am recruiting for a Lead CQV Consultant on a six-month contract in Bedford, MA. This is a fully on-site role with a competitive W2 hourly rate.

Key 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.
  • Push the team to be deadline-driven and accountable, identifying issues early and driving them to resolution.

Required Experience:

  • Strong commissioning and qualification (C&Q) experience with a primary focus on equipment validation.
  • Ability to own equipment validation packages and work independently in a matrixed environment.
  • Experience with aseptic smoke studies is beneficial but not required.
  • Understanding of CSV and FDA CSA guidelines would be a significant value add.

If you have the right experience and are interested, reach out to discuss further.

Hamish Corson

Senior Business Manager | USA | GxP Contract Division

+1 646 536 4736 (USA)

HCorson@i-pharmconsulting.com

Job Tags

Hourly pay, Contract work,

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