What are the responsibilities and job description for the Lead CQV Consultant position at i-Pharm Consulting?
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
