We are supporting a pharmaceutical manufacturer in Belgium who require an experienced CQV Consultant to join their engineering and validation team. You will be responsible for delivering commissioning, qualification, and validation activities on a critical manufacturing project to ensure GMP compliance and readiness for regulatory inspection.
This role is ideal for a consultant who thrives in fast-paced, compliance-driven environments and can hit the ground running on high-priority deliverables.
Key Responsibilities
* Plan, execute, and document commissioning, qualification, and validation activities (IQ/OQ/PQ).
* Develop and review validation protocols and reports for equipment, utilities, and systems.
* Support facility start-up, equipment upgrades, or tech transfer projects.
* Ensure all activities meet EU GMP, FDA, and ICH guidelines.
* Collaborate with engineering, QA, and production teams to ensure validation timelines are met.
* Prepare for and support regulatory inspections.
Skills & Experience
* 5+ years’ CQV experience in the pharmaceutical or biotech industry.
* Strong understanding of EU GMP regulations.
* Proven track record in executing IQ/OQ/PQ protocols.
* Experience with utilities (WFI, HVAC, compressed air) and/or process equipment.
* Excellent documentation and organisational skills.
Why Apply?
* Competitive daily rates and strong likelihood of extension.
* Opportunity to make a direct impact on product supply readiness.
* Collaborate with cross-functional teams on critical compliance deliverables.