Tech4Good Recruitment
CQV Consultant
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About the Company
A pharmaceutical manufacturing organisation operating within a GMP-regulated environment. The site is undertaking a focused remediation project to strengthen compliance and validation activities.
Why This Role Matters
You'll play a key role in delivering remediation activities that support GMP compliance and ensure critical facilities, equipment and systems remain fit for purpose.
The Role
You'll provide hands-on Commissioning, Qualification and Validation (CQV) support for a three-month remediation project at a GMP manufacturing site, working closely with site teams to progress and close validation activities.
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Key Responsibilities
- Execute CQV and remediation activities across relevant facilities, equipment, and systems at the manufacturing site.
- Prepare, review, and complete qualification and validation documentation required to support project delivery.
- Work with site stakeholders to identify, progress, and close remediation actions in line with GMP requirements.
Required Skills & Experience
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- Previous CQV experience within a GMP-regulated pharmaceutical or manufacturing environment.
- Hands-on experience delivering qualification and validation activities and associated documentation.
- Experience supporting remediation projects or resolving validation and compliance gaps within a regulated site.
What’s on Offer
- Three-month contract supporting a focused GMP remediation project.
- A hands-on assignment with direct involvement in site CQV and compliance activities.
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