Role: GCP Consultant
Location: Hybrid - 2 days onsite London
Company: Global Pharmaceutical Company
Are you passionate about driving quality and compliance in clinical development? We’re looking for a GCP Consultant to support the development and maintenance of robust clinical quality systems and ensure inspection readiness across global clinical operations.
🌟 What You’ll Do:
* Partner with the Head of Process Quality Excellence to shape and evolve quality and compliance infrastructure.
* Develop and revise SOPs, policies, and best practices to align with GCP, GLP, and PV standards.
* Collaborate cross-functionally with Global Quality, Patient Safety, Regulatory Affairs, and strategic partners.
* Lead inspection readiness activities across all GCSO functions.
* Support audits and inspections, including planning, representation, and response coordination.
✅ What You Bring:
* 8+ years of experience in the pharmaceutical industry, ideally in global Quality Assurance or Clinical Development.
* Deep knowledge of GCP and GVP, with hands-on experience in global audits and inspections.
* At least 2 years of experience writing SOPs.
* A proactive mindset and strong collaboration skills.
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.