QA Clinical Specialist at Qcs Staffing in Hampshire, England, United Kingdom | Kablio

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QA Clinical Specialist

Employer undisclosedRole managed by a recruiter

Support quality compliance, SOPs, and inspection readiness for global clinical operations.

11 days ago ago

Expert & Leadership (13+ years), Experienced (8-12 years)

Contractor

Hampshire, England, United Kingdom

Onsite

Your recruiting firm

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Founded with the aim of providing top-tier staffing solutions for diverse sectors.
Focus on long-term partnerships with clients, ensuring the right talent for specialized roles.
Expert in recruiting for both large-scale projects and niche, high-demand sectors.
Has become a trusted partner in sectors such as Industrial, Energy, and Infrastructure.
Notable for a rapid response to market demands and changing industry trends.
Experience in delivering recruitment services for large infrastructure and energy projects.
Specializes in sourcing skilled professionals for both permanent and temporary roles.
Recognized for working on complex and large-scale projects with a diverse client base.

About the client

About the client

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Role

Description

audit planning

inspection preparation

inspection readiness

quality policies

sop development

compliance infrastructure

Participate in Audit and Inspection planning with Global Quality.
Represent or ensure GCSO representation including preparation during audits/inspections (on-site at UCB by internal and external parties).
Lead and drive GCSO Inspection Readiness Activities across all GCSO functions working closely with the relevant inspection team(s).
Support the HPQE in GCSO quality and compliance infrastructure development; assist with creation/revision of appropriate quality and compliance policies, Standard Operating Procedures (SOPs), processes, and best practices as needed.

Requirements

gcp

gvp

pharma

quality assurance

clinical development

sop writing

In depth experience of GCP and GVP, including hands on experience in global GCP audits and/or inspections.
Extensive pharmaceutical experience, preferably in a global Quality Assurance or a Clinical Development setting.
Extensive experience in SOP writing essential.

Benefits

Information not given or found

Training + Development

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Interview process

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Visa Sponsorship

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Security clearance

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